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Archive for the ‘Chemical Biology and its relations to Metabolic Disease’ Category

A Great University engaged in Drug Discovery: University of Pittsburgh

 

Reporter and Curator: Larry H. Bernstein, MD, FCAP

 

The US-based pharmaceutical companies have been consolidating and now are moving offshore to reduce taxes and other costs.  A part of the problem has been the large cost of clinical trials, the failure to detect toxicities in the early phases, and late phase failure or drug resistance conferring short term success.  This has been at a rate above 60%.  The result is that Big Pharma is looking to recycling old drugs for repurposing. Whatever success can be obtained from this, there is a larger problem in not having a comprehensive biological understanding of the problems imposed by the complexity on a deeper understanding.  I present here a major university, very well recognized in genetics, proteomics, and experimental pathology engaged in the drug development effort with reasonable promise of successes.

 

Perspective On: A Drug Discovery Lab

As lab manager at the University of Pittsburgh Drug Discovery Institute (UPDDI), Celeste Reese and her team use high-content imaging strategies and work with many other labs both within the university and outside the university on a wide range of projects.

By Rachel Muenz | July 03, 2014

 

We try to use new technologies and approaches and quantitative systems pharmacology (QSP) to complement the traditional drug discovery strategies

We try to use new technologies and approaches and quantitative systems pharmacology (QSP) to complement the traditional drug discovery strategies

 

 

Finding Clinically Relevant Solutions

Hard work, teamwork, and a whole lot of multitasking help this lab overcome a tough economic environment

“We try to use new technologies and approaches and quantitative systems pharmacology (QSP) to complement the traditional drug discovery strategies that are used by the large pharmacy companies,” she explains, adding that, on average, they have seven to ten active projects going on at any given time. “Right now we have a metastatic breast cancer program, a head and neck cancer project, and a Huntington’s disease project. We do some zebra fish modeling, some development of novel HIV diagnostics, liver modeling, and a variety of other things.”

Those projects take place in the institute’s 11,000 square feet of space, which covers two floors of the building the institute occupies and includes a large open lab on the top floor and an imaging lab, automation lab, and tissue culture facility on the floor below. Working in that space are 34 staff, including seven faculty, four graduate students, and five undergraduates, with the rest made up of technical specialists, administrative staff, and Reese herself. As in many other labs, staff members have a wide range of education levels—from high school for the undergrads all the way up to extensive post-doctoral experience for the faculty, Reese says, adding that staff receive quite a bit of training when they begin.

“The university has a lot of training modules that we send people to for such things as chemical hygiene, safety, and blood-borne pathogens, even things like safe shipping,” she says. “Then there are modules like conflict of interest training and research integrity training, which are also provided by the university. In-house, we train everyone on our equipment and on the procedures and protocols that we use within our institute.”

Training the grads and undergrads on those lab procedures is a big part of Reese’s role as lab manager, a task that she considers one of the highlights of the position.

“I really like working with the graduate students who come into the lab,” Reese says. “They always have a fresh perspective and they’re always challenging established protocols. They’re fresh and enthusiastic.”

The Catalyst Express robot is used to load plates onto a high-content imaging platform.It was a similar enthusiasm for science that led Reese to pursue the field in university, which led to a job in a pharmacology lab after graduation, getting her interested in the drug discovery field and—after 14 years staying home to raise her children—eventually brought her to the UPDDI, where she has worked for the past eight years.

“I’ve always loved science in general but then after college I got the job in the pharmacology lab and I just really liked experimental design and problem solving and implementation—which eventually led into the lab management position,” says Reese, who has now been lab manager at the UPDDI for four years.

Because of her enjoyment of experimenting, along with her other management duties of looking after supplies and equipment, Reese also likes to keep a hand in what’s going on in the lab.

“I keep an active role in at least one of the research projects that we have going on,” she explains. “I find that that’s very helpful in the lab management area as well, because I see key things while I’m doing experiments that I normally wouldn’t see on a walkthrough.”

Blocking out the day

Liquid nitrogen cell bank.

Liquid nitrogen cell bank.

 

 

Liquid nitrogen cell bank.For Reese, scheduling chunks of time for certain tasks is critical in ensuring she meets her goals for the day.

“Time management’s key when you’re trying to cover as many roles as it takes to do this job,” she says. “I try to keep the mornings for the lab management tasks and then the afternoons are usually taken up with meetings, experimental design and implementation, or data analysis.”

That means Reese’s mornings typically involve coming in, checking on what’s happening in the lab, looking after the ordering of supplies for the week, and attending to any equipment problems and emails. Along with meetings, her afternoons are usually taken up with running or designing experiments or analyzing data. Of course, the rest of the staff have a variety of different roles.

A few programs and regular inventory checks help keep everything organized.

“One of the big tools we have is a purchasing program that we have developed in-house—an access program that we use and a similar one for equipment reservations and things like that,” Reese says. “We do a weekly inventory. We have two stockroom areas and we have two student workers who go out and stock all the individual work areas for people every day. And then we also have written protocols and established procedures for things like routine equipment maintenance and buffer preparations and such.”

She adds that the main challenge her lab faces is the same one that many other labs face—doing more with less in the current tough economic climate. For her lab, multitasking and teamwork are a big part of solving that issue.

“We just have really talented people here,” Reese says of her staff. “Everybody takes on a variety of roles. Everybody pitches in with things like routine equipment maintenance and … rather than having one person in each job, everybody covers a variety of tasks.” Because of that strong teamwork, Reese finds she doesn’t need to do much to motivate members of the lab.

“I don’t manage people—I just try to lead by example and try to take care of any issues that come up promptly rather than put things off,” she explains. “Everybody’s pretty self-motivated and hardworking here.”

An automated compound storage system is used to store the institute’s screening libraries.

An automated compound storage system is used to store the institute’s screening libraries.

 

six separate tissue culture facilities

six separate tissue culture facilities

 

 

 

 

 

 

 

 

 

 

 

An automated compound storage system is used to store the institute’s screening libraries. The UPDDI has six separate tissue culture facilities equipped with biosafety cabinets, incubators, and microscopes.

The tech side

Along with the aforementioned high-content imaging, Reese’s lab also uses automated liquid handling platforms, biosensors, microfluidics, and immunofluorescence and fluorescence microscopy, and they are starting to implement 3D cell culture strategies to tackle their many projects.

“These fluorescent proteins react to the physiological changes in the cell in real time,” Reese says of the lab’s work with biosensors. “And [with] microfluidics you actually have a moving system. The system is more clinically relevant— it’s a better model for the in vivo systems.”

By “clinically relevant” Reese says she basically means the center is trying to more closely model what is actually going on in the human body, rather than relying on traditional 2D cell culture models or high throughput methods. That focus on clinically relevant methods is a result of big changes in the pharmaceutical industry in recent years.

Top 5 Instruments in the Lab

  • GE InCell6000 Imaging System
  • Agilent (Velocity 11) Bravo Liquid Handling Platform
  • Thermo Scientific Multidrop Combi Dispenser
  • PerkinElmer EnVision 2103 Multilabel Plate Reader
  • Brooks (Matrical) Ministore Automated Compound  Management System

“In the drug discovery field in general, big pharma has been using the mass-scale high throughput screening for a long time and of course now we’re coming to the patent cliff for a lot of the pharmaceutical companies, when a lot of their moneymakers are going off patent,” Reese explains. “So here, we’re trying to move away from that high throughput screening toward a more high-content [screening] where we’re looking at more clinically relevant methods and QSP approaches for drug discovery.”

And the most interesting work the lab is doing right now?

“I would say the coolest thing we have going on is a liver microphysiology project,” Reese says. “We’re making a liver biomimetic, which will be integrated with other organ biomimetics to create a human-on-a-chip for use as a model for drug toxicity and other kinds of organ analysis.”

Categories: Research-Specific Labs

Tags: Drug Discovery Labs

 

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Reference Genes in the Human Gut Microbiome: The BGI Catalogue

Reporter: Aviva Lev-Ari, PhD, RN

An integrated catalog of reference genes in the human gut microbiome

Nature Biotechnology (2014) doi:10.1038/nbt.2942

Received 01 April 2014

Accepted 03 June 2014

Published online 06 July 2014

Article tools

Abstract

Many analyses of the human gut microbiome depend on a catalog of reference genes. Existing catalogs for the human gut microbiome are based on samples from single cohorts or on reference genomes or protein sequences, which limits coverage of global microbiome diversity. Here we combined 249 newly sequenced samples of the Metagenomics of the Human Intestinal Tract (MetaHit) project with 1,018 previously sequenced samples to create a cohort from three continents that is at least threefold larger than cohorts used for previous gene catalogs. From this we established the integrated gene catalog (IGC) comprising 9,879,896 genes. The catalog includes close-to-complete sets of genes for most gut microbes, which are also of considerably higher quality than in previous catalogs. Analyses of a group of samples from Chinese and Danish individuals using the catalog revealed country-specific gut microbial signatures. This expanded catalog should facilitate quantitative characterization of metagenomic, metatranscriptomic and metaproteomic data from the gut microbiome to understand its variation across populations in human health and disease.

SOURCE
Nature Biotechnology (2014) doi:10.1038/nbt.2942

 

BGI Scientists Expand Reference Genes for Human Microbiome

By Aaron Krol

July 14, 2014 | The Beijing Genomics Institute (BGI), China’s gene sequencing powerhouse, has released a set of reference genes for the human gut microbiome, in a catalogue that is substantially larger and covers a greater diversity of human populations than any previous resources. The work is described in a recentNature Biotechnology paper, “An integrated catalog of reference genes in the human gut microbiome,” by senior author Jun Wang of BGI-Shenzhen, while the reference itself is freely available at meta.genomics.cn.

A reference set of genes that have been found in organisms living in the human gut is an essential resource for profiling the species present in a person’s microbiota, and can also help to estimate their abundance and phylogenetic relationships, or to identify species that are correlated with aspects of human health. However, as the authors note, “there has been no comprehensive and uniformly processed database that can represent the human gut microbiota around the world.” The two largest previous reference catalogues, from the MetaHIT project and the Human Microbiome Project (HMP), have contained imperfectly sequenced and redundant genes, and have only sequenced samples taken from individuals from Europe and the U.S., respectively. The BGI team combined sequencing data from both of those projects with hundreds of Chinese samples from a study of diabetes, plus 249 newly-sequenced samples from Europe. In order to adequately cover the genomes of organisms that occur commonly in the human gut, but at such low abundance that few reads can be recovered from them, the team also integrated reference genomes of bacteria and archaea from the NCBI and EMBL databases for any species that were 90% covered by the combined samples used in this project.

The resulting catalogue, the Integrated Gene Catalogue (IGC), contains nearly 10 million unique genes — a greater than 70% increase over either the MetaHIT or HMP resources. Because of a stricter quality control pipeline, the IGC also eliminates large proportions of short or fragmented genes from the prior databases. When using the IGC to assemble metagenomes from both the sample sets used in the creation of the IGC, and three independent sample sets, in all cases between 74 and 81% of sequencing data could be mapped to the IGC. The authors suggest that this is “close to the maximum achievable mapping rates,” given the estimate that prokaryotic genomes have on average 87% gene content.

The impressive breadth of the IGC allows for some interesting observations. Individual samples used in the project contained roughly 760,000 genes on average, and any two samples would share roughly one third of those genes in common. Each sample contributed an average of 469 genes found in no other sample. As in other microbiome references, the species identity of most genes remains a mystery; only around 16% could be confidently assigned to a genus. While nearly all species found in a large proportion of samples were already known to be part of the human microbiota from previous studies, the wine-fermenting genus Oenococcus, found in 13.5% of samples in the IGC, had never previously been shown to live in the human gut.

Based on their experience creating the IGC, the BGI team offer a number of suggestions for future investigation of the human gut microbiome. They speculate that “we may have reached saturated coverage of core gene content and functions, but rare genes will continue to be discovered,” adding that most of the new genes included in the IGC were found in only a small minority of individuals. They also propose that, while deeper sequencing of individuals is a tempting way to get better read depth of low-abundance species, it may in fact be more cost-effective to simply sequence more samples at current read depths. In the case of the low-abundance genus Enterococcus, the IGC was able to improve coverage by over 70% thanks to a handful of samples where the genus was found in unexpectedly high abundance, a finding that may be repeated with other organisms.

Discovering more of these rare genes, the authors suggest, may shed a great deal of light on important functional differences between humans’ commensal organisms. While the genes of known function that are found at high frequency in the IGC tend to cover basic processes like metabolism and signal transduction, those found in fewer than 1% of individuals tend to be involved in adaptive processes, like DNA repair, antibiotic resistance, and responses to phages and the human immune system. Covering more human populations is also likely to yield new functional insights: in a comparison of Danish to Chinese samples, using the IGC as a map, genes highly divergent between the two groups tended to be involved in the metabolism of specific carbohydrates, amino acids, and vitamins, strongly suggesting a relationship with human diet.

“Similar to the field of human genetics, where the search for new alleles has progressed from common to rare,” the authors conclude, “our data indicate that cataloging of our ‘other genome,’ the human gut microbiome, is also entering the stage for identification of rare or individual-specific genes.”

With the IGC made available to all researchers around the world online, it is likely that in the coming months new studies will appear using the IGC as a reference map, helping to show whether outside groups find the new catalogue a useful and reliable tool for studying the human microbiome.

 SOURCE

 

 

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Loss of Normal Growth Regulation

Curator: Larry H Bernstein, MD, FCAP

 

 

Reposted from Dr. Melvin Crasso

Cells from most major human solid and hematologic malignancies exhibit abnormal cellular localization of a variety of oncogenic proteins, tumor suppressor proteins, and cell cycle regulators (Cronshaw et al. 2004, Falini et al 2006). For example, certain p53 mutations lead to localization in the cytoplasm rather than in the nucleus. This results in the loss of normal growth regulation, despite intact tumor suppressor function. In other tumors, wild-type p53 is sequestered in the cytoplasm or rapidly degraded, again leading to loss of its suppressor function. Restoration of appropriate nuclear localization of functional p53 protein can normalize some properties of neoplastic cells (Cai et al. 2008; Hoshino et al. 2008; Lain et al. 1999a; Lain et al. 1999b; Smart et al. 1999), can restore sensitivity of cancer cells to DNA damaging agents (Cai et al. 2008), and can lead to regression of established tumors (Sharpless & DePinho 2007, Xue et al. 2007). Similar data have been obtained for other tumor suppressor proteins such as forkhead (Turner and Sullivan 2008) and c-Abl (Vignari and Wang 2001). In addition, abnormal localization of several tumor suppressor and growth regulatory proteins may be involved in the pathogenesis of autoimmune diseases (Davis 2007, Nakahara 2009). CRMl inhibition may provide particularly interesting utility in familial cancer syndromes (e.g. , Li-Fraumeni Syndrome due to loss of one p53 allele,

BRCA1 or 2 cancer syndromes), where specific tumor suppressor proteins (TSP) are deleted or dysfunctional and where increasing TSP levels by systemic (or local) administration of CRMl inhibitors could help restore normal tumor suppressor function. Specific proteins and R As are carried into and out of the nucleus by specialized transport molecules, which are classified as importins if they transport molecules into the nucleus, and exportins if they transport molecules out of the nucleus (Terry et al. 2007;

Sorokin et al. 2007). Proteins that are transported into or out of the nucleus contain nuclear import/localization (NLS) or export (NES) sequences that allow them to interact with the relevant transporters. Chromosomal Region Maintenance 1 (Crml or CRM1), which is also called exportin-1 or Xpol, is a major exportin.

Overexpression of Crml has been reported in several tumors, including human ovarian cancer (Noske et al. 2008), cervical cancer (van der Watt et al. 2009), pancreatic cancer (Huang et al. 2009), hepatocellular carcinoma (Pascale et al. 2005) and osteosarcoma (Yao et al. 2009) and is independently correlated with poor clinical outcomes in these tumor types.

Inhibition of Crml blocks the exodus of tumor suppressor proteins and/or growth regulators such as p53, c-Abl, p21, p27, pRB, BRCA1, IkB, ICp27, E2F4, KLF5, YAP1, ZAP, KLF5, HDAC4, HDAC5 or forkhead proteins (e.g., FOX03a) from the nucleus that are associated with gene expression, cell proliferation, angiogenesis and epigenetics. Crml inhibitors have been shown to induce apoptosis in cancer cells even in the presence of activating oncogenic or growth stimulating signals, while sparing normal (untransformed) cells. Most studies of Crml inhibition have utilized the natural product Crml inhibitor Leptomycin B (LMB). LMB itself is highly toxic to neoplastic cells, but poorly tolerated with marked gastrointestinal toxicity in animals (Roberts et al. 1986) and humans (Newlands et al. 1996). Derivatization of LMB to improve drug-like properties leads to compounds that retain antitumor activity and are better tolerated in animal tumor models (Yang et al. 2007, Yang et al. 2008, Mutka et al. 2009). Therefore, nuclear export inhibitors could have beneficial effects in neoplastic and other proliferative disorders.

In addition to tumor suppressor proteins, Crml also exports several key proteins that are involved in many inflammatory processes. These include IkB, NF-kB, Cox-2, RXRa, Commdl, HIFl, HMGBl, FOXO, FOXP and others. The nuclear factor kappa B (NF-kB/rel) family of transcriptional activators, named for the discovery that it drives immunoglobulin kappa gene expression, regulate the mRNA expression of variety of genes involved in inflammation, proliferation, immunity and cell survival. Under basal conditions, a protein inhibitor of NF-kB, called IkB, binds to NF-kB in the nucleus and the complex IkB-NF-kB renders the NF-kB transcriptional function inactive. In response to inflammatory stimuli, IkB dissociates from the IkB-NF-kB complex, which releases NF-kB and unmasks its potent transcriptional activity. Many signals that activate NF-kB do so by targeting IkB for proteolysis (phosphorylation of IkB renders it “marked” for ubiquitination and then proteolysis). The nuclear IkBa-NF-kB complex can be exported to the cytoplasm by Crml where it dissociates and NF-kB can be reactivated. Ubiquitinated IkB may also dissociate from the NF-kB complex, restoring NF-kB transcriptional activity. Inhibition of Crml induced export in human neutrophils and macrophage like cells (U937) by LMB not only results in accumulation of transcriptionally inactive, nuclear IkBa-NF-kB complex but also prevents the initial activation of NF-kB even upon cell stimulation (Ghosh 2008, Huang 2000). In a different study, treatment with LMB inhibited IL-Ιβ induced NF-kB DNA binding (the first step in NF-kB transcriptional activation), IL-8 expression and intercellular adhesion molecule expression in pulmonary microvascular endothelial cells (Walsh 2008). COMMDl is another nuclear inhibitor of both NF-kB and hypoxia-inducible factor 1 (HIFl) transcriptional activity. Blocking the nuclear export of COMMDl by inhibiting Crml results in increased inhibition of NF-kB and HIFl transcriptional activity (Muller 2009).

Crml also mediates retinoid X receptor a (RXRa) transport. RXRa is highly expressed in the liver and plays a central role in regulating bile acid, cholesterol, fatty acid, steroid and xenobiotic metabolism and homeostasis. During liver inflammation, nuclear RXRa levels are significantly reduced, mainly due to inflammation-mediated nuclear export of RXRa by Crml . LMB is able to prevent IL-Ιβ induced cytoplasmic increase in RXRa levels in human liver derived cells (Zimmerman 2006).

The role of Crml -mediated nuclear export in NF-kB, HIF-1 and RXRa signalling suggests that blocking nuclear export can be potentially beneficial in many inflammatory processes across multiple tissues and organs including the vasculature (vasculitis, arteritis, polymyalgia rheumatic, atherosclerosis), dermatologic (see below), rheumatologic

(rheumatoid and related arthritis, psoriatic arthritis, spondyloarthropathies, crystal arthropathies, systemic lupus erythematosus, mixed connective tissue disease, myositis syndromes, dermatomyositis, inclusion body myositis, undifferentiated connective tissue disease, Sjogren’s syndrome, scleroderma and overlap syndromes, etc.).

CRM1 inhibition affects gene expression by inhibiting/activating a series of transcription factors like ICp27, E2F4, KLF5, YAP1, and ZAP.

Crml inhibition has potential therapeutic effects across many dermatologic syndromes including inflammatory dermatoses (atopy, allergic dermatitis, chemical dermatitis, psoriasis), sun-damage (ultraviolet (UV) damage), and infections. CRMl inhibition, best studied with LMB, showed minimal effects on normal keratinocytes, and exerted anti-inflammatory activity on keratinocytes subjected to UV, TNFa, or other inflammatory stimuli (Kobayashi & Shinkai 2005, Kannan & Jaiswal 2006). Crml inhibition also upregulates NRF2 (nuclear factor erythroid-related factor 2) activity, which protects keratinocytes (Schafer et al. 2010, Kannan & Jaiswal 2006) and other cell types (Wang et al. 2009) from oxidative damage. LMB induces apoptosis in keratinocytes infected with oncogenic human papillomavirus (HPV) strains such as HPV 16, but not in uninfected keratinocytes (Jolly et al. 2009).

Crml also mediates the transport of key neuroprotectant proteins that may be useful in neurodegenerative diseases including Parkinson’s disease (PD), Alzheimer’s disease, and amyotrophic lateral sclerosis (ALS). For example, by (1) forcing nuclear retention of key neuroprotective regulators such as NRF2 (Wang 2009), FOXA2 (Kittappa et al. 2007), parking in neuronal cells, and/or (2) inhibiting NFKB transcriptional activity by sequestering IKB to the nucleus in glial cells, Crml inhibition could slow or prevent neuronal cell death found in these disorders. There is also evidence linking abnormal glial cell proliferation to abnormalities in CRMl levels or CRMl function (Shen 2008).

Intact nuclear export, primarily mediated through CRMl, is also required for the intact maturation of many viruses. Viruses where nuclear export, and/or CRMl itself, has been implicated in their lifecycle include human immunodeficiency virus (HIV), adenovirus, simian retrovirus type 1, Borna disease virus, influenza (usual strains as well as H1N1 and avian H5N1 strains), hepatitis B (HBV) and C (HCV) viruses, human papillomavirus (HPV), respiratory syncytial virus (RSV), Dungee, Severe Acute Respiratory Syndrome coronavirus, yellow fever virus, West Nile virus, herpes simplex virus (HSV), cytomegalovirus (CMV), and Merkel cell polyomavirus (MCV). (Bhuvanakantham 2010, Cohen 2010, Whittaker 1998). It is anticipated that additional viral infections reliant on intact nuclear export will be uncovered in the future.

The HIV-1 Rev protein, which traffics through nucleolus and shuttles between the nucleus and cytoplasm, facilitates export of unspliced and singly spliced HIV transcripts containing Rev Response Elements (RRE) RNA by the CRMl export pathway. Inhibition of Rev-mediated RNA transport using CRMl inhibitors such as LMBor PKF050-638 can arrest the HIV-1 transcriptional process, inhibit the production of new HIV-1 virions, and thereby reduce HIV-1 levels (Pollard 1998, Daelemans 2002). Dengue virus (DENV) is the causative agent of the common arthropod-borne viral disease, Dengue fever (DF), and its more severe and potentially deadly Dengue hemorrhagic fever (DHF). DHF appears to be the result of an over exuberant inflammatory response to DENV. NS5 is the largest and most conserved protein of DENV. CRMl regulates the transport of NS5 from the nucleus to the cytoplasm, where most of the NS5 functions are mediated. Inhibition of CRMl -mediated export of NS5 results in altered kinetics of virus production and reduces induction of the inflammatory chemokine interleukin-8 (IL-8), presenting a new avenue for the treatment of diseases caused by DENV and other medically important flaviviruses including hepatitis C virus (Rawlinson 2009).

Other virus-encoded RNA-binding proteins that use CRMl to exit the nucleus include the HSV type 1 tegument protein (VP 13/14, or hUL47), human CMV protein pp65, the SARS Coronavirus ORF 3b Protein, and the RSV matrix (M) protein (Williams 2008, Sanchez 2007, Freundt 2009, Ghildyal 2009).

Interestingly, many of these viruses are associated with specific types of human cancer including hepatocellular carcinoma (HCC) due to chronic HBV or HCV infection, cervical cancer due to HPV, and Merkel cell carcinoma associated with MCV. CRMl inhibitors could therefore have beneficial effects on both the viral infectious process as well as on the process of neoplastic transformation due to these viruses.

CRMl controls the nuclear localization and therefore activity of multiple DNA metabolizing enzymes including histone deacetylases (HDAC), histone acetyltransferases (HAT), and histone methyltransferases (HMT). Suppression of cardiomyocyte hypertrophy with irreversible CRMl inhibitors has been demonstrated and is believed to be linked to nuclear retention (and activation) of HDAC 5, an enzyme known to suppress a hypertrophic genetic program (Monovich et al. 2009). Thus, CRMl inhibition may have beneficial effects in hypertrophic syndromes, including certain forms of congestive heart failure and hypertrophic cardiomyopathies.

 

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Larry H. Bernstein, MD, FCAP, Curator

http://pharmaceuticalinnovation/6/7/2014/Omega-3 fatty acids, depleting the source, and protein insufficiency in renal disease

 

This article is concerned only with updating the importance of key nutrients for maintenance of health. Nutritional losses are associated with memory loss, impaired immunity, and loss of lean body mass.

 

Low levels of omega-3 fatty acids may cause memory problems

Disease and ConditionsGeneral Diet • Tags: Alzheimer’s diseaseAmerican Academy of NeurologyDocosahexaenoic acidMagnetic resonance imagingNeurologyOmega-3 fatty acid, United States Environmental Protection AgencyUniversity of California Los Angeles

09 Mar 2012

 

ST. PAUL, Minn. – A diet lacking in omega-3 fatty acids, nutrients commonly found in fish, may cause your brain to age faster and lose some of its memory and thinking abilities, according to a study published in the February 28, 2012, print issue of Neurology®, the medical journal of the American Academy of Neurology. Omega-3 fatty acids include the nutrients called docosahexaenoic acid (DHA) and eicosapentaenoic acid (EPA).

salmon dinner

salmon dinner

 

 

 

 

 

 

 

 

 

“People with lower blood levels of omega-3 fatty acids had lower brain volumes that were equivalent to about two years of structural brain aging,” said study author Zaldy S. Tan, MD, MPH, of the Easton Center for Alzheimer’s Disease Research and the Division of Geriatrics, University of California at Los Angeles.

For the study, 1,575 people with an average age of 67 and free of dementia underwent MRI brain scans. They were also given tests that measured mental function, body mass and the omega-3 fatty acid levels in their red blood cells.

The researchers found that people whose DHA levels were among the bottom 25 percent of the participants had lower brain volume compared to people who had higher DHA levels. Similarly, participants with levels of all omega-3 fatty acids in the bottom 25 percent also scored lower on tests of visual memory and executive function, such as problem solving and multi-tasking and abstract thinking.

Related articles

 

Mechanisms of muscle wasting in chronic kidney disease.

Xiaonan H WangWilliam E Mitch

Nature Reviews Nephrology (Impact Factor: 7.94). 07/2014; DOI: 10.1038/nrneph.2014.112

Source: PubMed

ABSTRACT In patients with chronic kidney disease (CKD), loss of cellular proteins increases the risks of morbidity and mortality. Persistence of muscle protein catabolism in CKD results in striking losses of muscle proteins as whole-body protein turnover is great; even small but persistent imbalances between protein synthesis and degradation cause substantial protein loss. No reliable methods to prevent CKD-induced muscle wasting currently exist, but mechanisms that control cellular protein turnover have been identified, suggesting that therapeutic strategies will be developed to suppress or block protein loss. Catabolic pathways that cause protein wasting include activation of the ubiquitin-proteasome system (UPS), caspase-3, lysosomes and myostatin (a negative regulator of skeletal muscle growth). These pathways can be initiated by complications associated with CKD, such as metabolic acidosis, defective insulin signalling, inflammation, increased angiotensin II levels, abnormal appetite regulation and impaired microRNA responses. Inflammation stimulates cellular signalling pathways that activate myostatin, which accelerates UPS-mediated catabolism. Blocking this pathway can prevent loss of muscle proteins. Myostatin inhibition could yield new therapeutic directions for blocking muscle protein wasting in CKD or disorders associated with its complications.

 

We’re Fishing the Oceans Dry. It’s Time to Reconsider Fish Farms.

Food and Agriculture Organization of the United Nations -State of World Fisheries and Aquaculture  2014

Food and Agriculture Organization of the United Nations -State of World Fisheries and Aquaculture 2014

 

 

 

 

 

 

 

 

 

 

 

 

Aquaculture has gotten much greener, with American innovators leading the way.

— Text by Maddie Oatman; video by Brett Brownell

| Wed Jul. 2, 2014 6:00 AM EDT    MotherJones.com

 

When I meet Kenny Belov mid-morning at San Francisco’s Fisherman’s Wharf, the boats that would normally be out at sea chasing salmon sit tethered to their docks. The steady breeze coursing through the bay belies choppier conditions farther out—so rough that the local fishermen threw in the towel for the fifth morning in a row. Belov scans the horizon as he explains this, feet away from the warehouse of his sustainable seafood company, TwoXSea. Because his business hinges on what local fishermen can bring in, he’s used to coping with wild fish shortages.

If we continue to fish at the current pace, some scientists predict we’ll be facing oceans devoid of edible marine creatures by 2050.

But unlike these fishermen, Belov has a stash of treasure in his warehouse, as he soon shows me: a golf-cart-size container of plump trout, their glossy bodies still taut from rigor mortis. The night before, Belov drove north to Humboldt to help “chill kill” the fish by submerging them live into barrels of slushy ice water. Belov can count on shipments of these McFarland Springs trout every week—because he helped grow them himself on a farm.

For many consumers, aquaculture lost its appeal after unappetizing news spread about commercial fish farms—like fish feed’s pressure on wild resources, overflowing waste, toxic buildup in the water, and displacement of natural species. But consider this: Our appetite for seafood continues to rise. Globally, we’ve hungered for 3.2 percent more seafood every year for the last five decades, double the rate of our population. Yet more than four-fifths of the world’s wild fisheries are overexploited or fully exploited (yielding the most fish possible with no expected room for growth). Only 3 percent of stocks are considered underexploited—meaning they have any significant room for expansion. If we continue to fish at the current pace, some scientists predict we’ll be facing oceans devoid of edible marine creatures by 2050.

Aquaculture could come to the rescue. The Food and Agriculture Organization of the United Nations predicts that farmed fish will soon surpass wild-caught; by 2030, aquaculture may produce more than 60 percent of fish we consume as food.

Food and Agriculture Organization of the United Nations “State of World Fisheries and Aquaculture” 2014 report

One of the most pressing concerns about aquaculture, though, is that many farmed fish are raised on a diet of 15 million tons a year of smaller bait fish—species like anchovies and menhaden. These bait—also known as forage fish—are ground up and converted into a substance called fishmeal. It takes roughly five pounds of them to produce one pound of farmed salmon. Bait fish are also used for nonfood products like pet food, makeup, farm animal feed, and fish oil supplements.

Forage fish are a “finite resource that’s been fully utilized.”

It may appear as though the ocean enjoys endless schools of these tiny fish, but they too have been mismanaged, and their populations are prone to collapse. They’re a “finite resource that’s been fully utilized,” says Mike Rust of NOAA’s fisheries arm. Which is disturbing, considering that researchers like those at Oceana argue that forage fish may play an outsize role in maintaining the ocean’s ecological balance, including by contributing to the abundance of bigger predatory fish.

And that’s where Belov’s trout come in: Though he swears no one can taste the difference, his fish are vegetarians. That means those five pounds of forage fish can rest easy at sea. It also means that the trout don’t consume some of the other rendered animal proteins in normal fishmeal pellets: bone meal, feather meal, blood meal, and chicken byproducts.

Belov and McFarland Springs’ owner David McFarland were inspired to switch to vegetarian feed in part by Rick Barrows, a USDA researcher. About six years ago, recounts Barrows, several USDA studies confirmed that fish rely on nutrients—vitamins, minerals, fatty acids, and protein—rather than fishmeal or fish oil, to thrive. If those nutrients could be found in other products, including purely plant-based substances, then aquaculture might not be so dependent on feeding fish other smaller fish.

Barrows and team began to test about 50 potential materials a year, and now have a database of 140 that anyone can browse through online. Belov was one of their first commercial partners. The plant-based food fed to McFarland Springs’ trout consists of a hearty blend of marine algae, freshwater micro algae, vitamins, minerals, flax, flax oil, corn, and nut waste. The resulting complete protein means the trout’s omega 3s are high and their omega 6s are low—a ratio that’s said to enhance anti-inflammatory properties. And “they don’t have the concentration of heavy metals that come from the bait fish,” Belov says. I took one of his rosy fillets home and turned it into trout lox; find the recipe here.

McFarland Springs manages the trout’s waste by funneling it out into a natural sagebrush pasture where it composts the soil.

Belov’s fish feed includes California nuts that are too broken or disfigured to be sold.

Barrows thinks region-specific material for this type of feed offers the most potential. For instance, his team learned that around 5 percent of California nuts can’t be sold because they’re broken or disfigured. They realized they could repurpose excess nut parts for the trout feed; the nut bits helped round out the complete protein. Lately, Barrows has become especially excited about turning barley surplus from the beer industry—which comes at a cheap price in Montana, where he’s based—into a feed-grade concentrate for trout feed.

“You can get just as much growth rate out of fishmeal-free feeds as fishmeal,” says Barrows. And his lab has proven as much with eight different fish species: cobia, Florida pompano, coho salmon, Atlantic salmon, walleye, yellowtail, and White seabass.

But the price difference still stands in the way for many fish farmers. Belov pays slightly more than $1/pound for his plant-based feed, whereas fishmeal pellets average around $0.71/pound. He sells his trout for $6.95/pound, about a dollar more than conventional. But he’s well positioned in the affluent Bay Area, and he usually sells out of his McFarland Springs trout well before the end of each week. As innovation continues in the realm of plant-based feeds, he’s hopeful, along with Barrows, that the price of the pellets will continue to drop.

Here in the United States, we consume plenty of farmed fish already, but only 5 percent of it is sourced domestically. “If we didn’t import so much farmed seafood,” implored Four Fish author Paul Greenberg in a recent New York Times op-ed, “we might develop a viable, sustainable aquaculture sector of our own.” It doesn’t just boil down to economics: The locations we generally export from, like China and South Asia, don’t have near the stringent environmental and health regulations as the US. “Growing more seafood at home would help with trade deficit, but also we could control the safety more,” says Barrows.

Though our current aquaculture sector is relatively tiny, US farmers are in a better position to innovate, because we have a sophisticated animal nutrition research center and feed sector, says NOAA’s Rust. “We’re the leading technical country in the world on feed.”

Belov wasn’t always open to aquaculture, and he still feels that fish—such as some salmon—with healthy wild fisheries attached to them should never be farmed. That way, environmentally responsible fishermen can stay in business. His long-term strategy for sustainable seafood? Draw from the “amazing [wild] fisheries that exist, and then you backfill with intelligent aquaculture, and yes, you can feed the planet with sustainable marine products.” Which may take more work, but as he puts it, “We depleted the ocean. It wasn’t anybody else’s fault. So it’s our job to fix it.”

 

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Larry H Bernstein, MD, FCAP

http://pharmaceuticalintelligence.com/6-19-2014/larryhbern/Gene Switch Takes Blood Cells to Leukemia and Back Again

Kevin Mayer

 

Summary

Loss-of-function mutations in a gene called Pax5 have been known to drive normal blood cells to turn into leukemia cells. Such mutations are permanent, so it remained unclear whether an initial, temporary loss of function would instigate an irreversible cascade of events leading to an accumulation of undifferentiated lymphoblasts, or whether an ongoing loss of function would be needed to maintain the disease state.

 

With the publication of a new study, the question has become more than academic. The study, by researchers at Melbourne’s Walter and Eliza Hall Institute, has not only shown that switching off Pax5 causes cancer in a murine model of B-progenitor acute lymphoblastic leukemia (B-ALL), it has also demonstrated that switching on Pax5 essentially cures the disease.

The results of the study appeared June 15 in the journal Genes & Development, in an article entitled “Pax5 loss imposes a reversible differentiation block in B-progenitor acute lymphoblastic leukemia.” The article described how the researchers used transgenic RNAi to reversibly suppress endogenous Pax5 expression in the hematopoietic compartment of mice, which cooperates with activated signal transducer and activator of transcription 5 (STAT5) to induce B-ALL.

“In this model, restoring endogenous Pax5 expression in established B-ALL triggers immunophenotypic maturation and durable disease remission by engaging a transcriptional program reminiscent of normal B-cell differentiation,” wrote the authors. “Notably, even brief Pax5 restoration in B-ALL cells causes rapid cell cycle exit and disables their leukemia-initiating capacity.”

Institute researcher Grace Liu noted that Pax5, which is frequently “lost” in childhood B-ALL, is essential for normal development of B cells. “When Pax5 function is compromised, developing B cells can get trapped in an immature state and become cancerous,” she said. “We have shown that restoring Pax5 function, even in cells that have already become cancerous, removes this ‘block,’ and enables the cells to develop into normal white blood cells.”

Simply restoring Pax5 sufficed to normalize cancer cells. That is, re-engaging the stalled differentiation program in immature white blood cells restored normal development “despite the presence of additional oncogenic lesions.”

Institute researcher Ross Dickins, Ph.D., said that forcing B-ALL cells to resume their normal development could provide a new strategy for treating leukemia: “While B-ALL has a relatively good prognosis compared with other cancers, current treatments can last years and have major side effects. By understanding how specific genetic changes drive B-ALL, it may be possible to develop more specific treatments that act faster with fewer side effects.”

“It is very difficult to develop drugs that restore the function of genes that are lost during cancer development,” Dr. Dickins added. “However, by understanding the mechanisms by which Pax5 loss causes leukemia, we can begin to look at ways of developing drugs that could have the same effect as restoring Pax5 function.”

Pax5 is just one of about 100 genes known to suppress human tumors. Now that Pax5 has been scrutinized with genetic switch technology, the researchers speculate that similar technology could be used to characterize other tumor suppressor genes.

 

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Koala, The Tree Hugger – Why?

Reporter: Aviva Lev-Ari, PhD, RN

 

This article is dedicated to Dr. Larry H Bernstein

https://www.google.com/search?site=&tbm=isch&source=hp&biw=1320&bih=825&q=Koala&oq=Koala&gs_l=img.3…4139.4839.0.5191.5.5.0.0.0.0.0.0..0.0….0…1ac.1.45.img..5.0.0.4WdTasUvIxM

 

Why Koalas Hug Trees

 

Editor’s Recommendations

 

SOURCE

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Cancer Labs at School of Medicine @ Technion: Janet and David Polak Cancer and Vascular Biology Research Center

Cancer Labs at School of Medicine @ Technion

Reporter: Aviva Lev-Ari, PhD, RN

Article ID #139: Cancer Labs at School of Medicine @ Technion: Janet and David Polak Cancer and Vascular Biology Research Center. Published on 5/28/2014

WordCloud Image Produced by Adam Tubman

Janet and David Polak Cancer and Vascular Biology Research CenterThe Rappaport Faculty of Medicine Research Institute and Faculty of Medicine, Technion – Israel Institute of Technology, Haifa, Israel

The center was established in 2003 to promote an in-depth interdisciplinary basic and clinical research on the control of cellular and molecular processes that are involved in cancer initiation and progression. We strongly believe that the understanding of basic biological processes that underlie normal development and their deregulation in cancer, is crucial for our ability to identify molecular targets for early detection, intervention, and cure of the disease. We are interested in a broad view of cancer – from the single malignantly transformed cell and its microenvironment, through the entire tumor in the animal. We focus on targeted ubiquitin-mediated degradation of key regulatory proteins that are involved in malignant transformation [Prof. Aaron Ciechanover (Nobel Prize in Chemistry 2004)], angiogenesis and cancer progression (Prof. Gera Neufeld), metastasis and tumor microenvironment (Prof. Israel Vlodavsky), as well as genetic and genomic dissection of embryonic and cancer transcriptional networks (Dr. Amir Orian). Towards these objectives, we combine molecular, biochemical, cell biological with Drosophila genetic and genomics experimental approaches, as well as employing advanced models of angiogenesis and metastasis.

We believe that scientific excellence and collegiality go together. Therefore, the center has an open and friendly atmosphere, creating a highly stimulating environment. The center is located in the 11th Floor of the Rappaport Faculty of Medicine building. It currently trains 45 graduate students, post-doctoral fellows, clinicians and researchers that are at the heart of our research. Formal and informal collaborations between individuals and laboratories are on-going and encouraged. We are running a series of joint seminars to which we invite researchers from Israel and abroad. The Center has advanced state-of-the-art microscopic and image analysis equipment, as well as other shared pieces of infrastructural equipment . The center is an integral part of the Faculty of Medicine and the Rappaport Research Institute which are home for excellent research groups, and enjoys their advanced Interdepartmental Equipment Unit. It is also adjacent to the Rambam Medical Center – the major hospital in the north of Israel – which provides us with access to rich clinical material and collaboration with clinicians. Many of them spend active research periods in our laboratories and bring the bench closer to the patient bed and vice versa. The Center is in an active phase of growth, and offers excellent research opportunities, space and facilities for students, post-doctoral fellows, and physicians.

Research Groups

The Ubiquitin System and Cellular Protein Turnover and Interactions

Immunity and Host Defense

Cardiovascular Biology

The Central Nervous System in Health and Disease

Developmental Biology and Cancer Research

Genetics

SOURCE 

http://www.rappaport.org.il/Rappaport/Templates/ShowPage.asp?DBID=1&TMID=842&FID=76

The cancer and vascular biology research center was established in 2003 to promote an in-depth interdisciplinary basic and clinical research on the control of cellular and molecular processes that are involved in cancer development and progression. Our goal is to advance knowledge in fundamental biological questions that are highly relevant for cancer.

The cancer and vascular biology research center was established in 2003 to promote an in-depth interdisciplinary basic and clinical research on the control of cellular and molecular processes that are involved in cancer development and progression. Our goal is to advance knowledge in fundamental biological questions that are highly relevant for cancer.

SOURCE

http://www.technioncancer.co.il/index.php

Home  >>  Research Groups

Aaron Ciechanover
Protein Turnover

Intracellular protein degradation and mechanisms of cancer
Israel Vlodavsky
Cancer Biology

Impact of heparanase and the tumor microenvironment on cancer progression: Basic aspects and clinical implications
Gera Neufeld
Tumor Progression & Angiogenesis

Blood vessels and tumor progression: The neuropilin connection
Amir Orian
Genetic Networks

Genetic networks in development and cancer
Home
About the Cancer Centers
Research Groups
Administration / Contact
Join – Us
Seminars and Events
Links
Beyond Science
Friends and supporters

Ms. Sigal Alfasi – Izrael, Center’s coordinator
e-mail: gsigal@tx.technion.ac.il
Tel: +972-4-829-5424
Fax: +972-4-852-3947

SOURCE

http://www.technioncancer.co.il/ResearchGroups.php

Yuval Shaked, PhD

Assistant Professor of Molecular Pharmacology

PhD, 2004 – Hebrew University, Israel

Understanding host – tumor interactions during cancer therapy

Personalized medicine holds promise of better cures with fewer side effects for many diseases. Individualized cancer therapy is sometimes utilized after multiple attempts of standard therapies and is based on several considerations, such as tumor type, acquired resistance to a specific therapy, previous treatment protocols, and other tumor-related factors. We have recently demonstrated that many cancer therapies can induce pro-tumorigenic or metastatic effects that derive not only from the tumor cells themselves, but also from host cells within the tumor microenvironment. The focus of research in my laboratory is to identify, characterize, and seek ways to block such pro-tumorigenic host effects observed after anti-cancer therapy, and thus potentially improve the outcome of current cancer therapies. Our findings may foster a paradigm shift in cancer therapy by minimizing the gap between preclinical findings and the clinical setting, laying the foundation for development of entirely new strategies for improving cancer therapy.

SOURCE

http://www.rappaport.org.il/Rappaport/Templates/ShowPage.asp?DBID=1&TMID=610&FID=77&PID=0&IID=1268

 

Other Related articled published on this Open Access Online Scientific Journal included the following:

D&D NT’s Solution: Galectin Proteins for Therapy and Diagnosis of Autoimmune Inflammatory and Cancer Diseases, Dr. Itshak Golan, CEO

http://pharmaceuticalintelligence.com/2014/05/28/dd-nts-solution-galectin-proteins-for-therapy-and-diagnosis-of-autoimmune-inflammatory-and-cancer-diseases-dr-itshak-golan-ceo/

MaimoniDex RA:  Monoclonal Antibodies for Therapy and Diagnosis of Cancer and Autoimmune Inflammatory Diseases – Dr. Itshak Golan, CEO

http://pharmaceuticalintelligence.com/2014/05/28/maimonidex-ra-monoclonal-antibodies-for-therapy-and-diagnosis-of-cancer-and-autoimmune-inflammatory-diseases-dr-itshak-golan-ceo/

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Immunity and Host Defense – A Bibliography of Research @Technion

Reporter: Aviva Lev-Ari, PhD, RN

Article ID #138: Immunity and Host Defense – A Bibliography of Research @Technion. Published on 5/27/2014

WordCloud Image Produced by Adam Tubman

 

 

 

Antigen-Dependent Integration of Opposing Proximal TCR-Signaling Cascades Determines the Functional Fate of T Lymphocytes

2014

Shai Shen-Orr, PhD
Authors : Wolchinsky R, Hod-Marco M, Oved K, Shen-Orr SS, Bendall SC, Nolan GP, Reiter Y.
J Immunol. 2014 Mar 1;192(5):2109-19.
Identification of functionally important conserved trans-membrane residues of bacterial P(IB) -type ATPases

2013

Oded Lewinson, PhD
Authors : Zhitnitsky D, Lewinson O.
Mol Microbiol. 2013 Dec 19. doi: 10.1111/mmi.12495. [Epub ahead of print] PubMed PMID: 24350798.
Variability in the immune system: of vaccine responses and immune states

2013

Shai Shen-Orr, PhD
Authors : Shen-Orr SS, Furman D.
Curr Opin Immunol. 2013 Aug;25(4):542-7.
Computational deconvolution: extracting cell type-specific information from heterogeneous samples.

2013

Shai Shen-Orr, PhD
Authors : Shen-Orr SS, Gaujoux R.
Curr Opin Immunol. 2013 Oct 19. [Epub ahead of print] PubMed PMID: 24148234.
Challenges and promise for the development of human immune monitoring.

2013

Shai Shen-Orr, PhD
Authors : Shen-Orr S.
Rambam Maimonides Med J. 2012 Oct 31;3(4):e0023.
Homeostatic regulation of aging and rejuvenation in the B lineage cells

2013

Doron Melamed, PhD
Authors : Melamed D.
Crit Rev Immunol. 2013;33(1):41-56.
Variability in the immune system: of vaccine responses and immune states

2013

Shai Shen-Orr, PhD
Authors : Shen-Orr S, Furman D.
Curr Opin Immunol. 2013 Aug 13. doi:pii: S0952-7915(13)00113-1.
A single intact ATPase site of the ABC transporter BtuCD drives 5% transport activity yet supports full in-vivo vitamin B12 utilization.

2013

Oded Lewinson, PhD
Authors : Tal N, Ovcharenko E, Lewinson O.
Proc Natl Acad Sci U S A. (March 19 Epub ahead of print)
Apoptosis and other immune biomarkers predict influenza vaccine responsiveness.

2013

Shai Shen-Orr, PhD
Authors : Furman D, Jojic V, Kidd B, Shen-Orr S, Price J, Jarrell J, Tse T, Huang H, Lund P, Maecker HT, Utz PJ, Dekker CL, Koller D, Davis MM.
Molecular Systems Biology. 9, 659
The dual roles of inflammatory cytokines and chemokines in the regulation of autoimmune diseases and their clinical implications.

2013

Nathan Karin, PhD
Authors : Shachar, I., and N. Karin.
J Leukoc Biol 93:51-61.
Two molybdate/tungstate ABC transporters that interact very differently with their substrate binding proteins.

2013

Oded Lewinson, PhD
Authors : Vigonsky, Ovcharenko E, Lewinson O.
Proc Natl Acad Sci U S A. (March 19 Epub ahead of print)
Dissecting the Autocrine and Paracrine Roles of the CCR2-CCL2 Axis in Tumor Survival and Angiogenesis.

2012

Nathan Karin, PhD
Authors : Izhak, L., G. Wildbaum, S. Jung, A. Stein, Y. Shaked, and N. Karin.
PloS one 7:e28305
Dose-related effects of hyperoxia on the lung inflammatory response in septic rats

2012

Nitza Lahat, PhD
Authors : Waisman D, Brod V, Rahat MA, Amit-Cohen BC, Lahat N, Rimar D, Menn-Josephy H, David M, Lavon O, Cavari Y, Bitterman H.
Shock. 2012 Jan;37(1):95-102.
Robust and sensitive analysis of xMap bead arrays using SAxCyB.

2012

Shai Shen-Orr, PhD
Authors : Won JH, Goldberger O, Shen-Orr SS, David MM, Olshen RA.
Proc Natl Acad Sci U S A. 109, 2848-53.
The Entamoeba histolytica methylated LINE-binding protein EhMLBP provides protection against heat shock

2012

Serge Ankri, PhD
Authors : Katz S, Kushnir O, Tovy A, Siman Tov R, Ankri S.
Cell Microbiol. 2012 Jan;14(1):58-70
Hypoxia increases membranal and secreted HLA-DR in endothelial cells, rendering them T-cell activators.

2011

Nitza Lahat, PhD
Authors : Lahat N, Bitterman H, Weiss-Cerem L, Rahat MA.
Transpl Int. 2011 Oct;24(10):1018-26.
The Entamoeba histolytica methylated LINE-binding protein EhMLBP provides protection against heat shock.

2011

Serge Ankri, PhD
Authors : Katz S, Kushnir O, Tovy A, Siman Tov R, Ankri S.
Cell Microbiol. 2011 Sep 8. [Epub ahead of print]
Dose-Related Effects of Hyperoxia on the Lung Inflammatory Response in Septic Rats. Shoc

2011

Nitza Lahat, PhD
Authors : Waisman D, Brod V, Rahat MA, Amit-Cohen BC, Lahat N, Rimar D, Menn-Josephy H, David M, Lavon O, Cavari Y, Bitterman H.
2011 Sep 3. [Epub ahead of print]
Glucose starvation boosts Entamoeba histolytica virulence.

2011

Serge Ankri, PhD
Authors : Tovy A, Hertz R, Siman-Tov R, Syan S, Faust D, Guillen N, Ankri S.
PLoS Negl Trop Dis. 2011 Aug;5(8):e1247.
The binding activity of Mel-18 at the Il17a promoter is regulated by the integrated signals of the TCR and polarizing cytokines.

2011

Eur J Immunol. 2011 Aug;41(8):2424-35.
phosphorylation of SLP-76 at tyrosine 173 is required for activation of T and mast cells.

2011

Deborah Yablonski, PhD
Authors : Sela M, Bogin Y, Beach D, Oellerich T, Lehne J, Smith-Garvin JE, Okumura M, Starosvetsky E, Kosoff R, Libman E, Koretzky G, Kambayashi T, Urlaub H, Wienands J, Chernoff J, Yablonski D. Sequential
EMBO J. 2011 Jul 1;30(15):3160-72.
The binding activity of Mel-18 at the Il17a promoter is regulated by the integrated signals of the TCR and polarizing cytokines.

2011

Orly Avni, PhD
Authors : Hod-Dvorai R, Jacob E, Boyko Y, Avni O.
Eur J Immunol. 2011 Jun 15. [Epub ahead of print]
MMP expression in leaking filtering blebs and tears after glaucoma filtering surgery.

2011

Nitza Lahat, PhD
Authors : Mathalone N, Marmor S, Rahat MA, Lahat N, Oron Y, Geyer O.
Graefes Arch Clin Exp Ophthalmol. 2011 Mar 31. [Epub ahead of print]
B cell depletion reactivates B lymphopoiesis in the BM and rejuvenates the B lineage in aging.

2011

Doron Melamed, PhD
Authors : Keren Z, Naor S, Nussbaum S Golan K, Itkin T, Sasaki Y, Schmidt-Supprian M, Lapidot T, Melamed D.
Blood 117, 3104 – 3112.
Chronic B cell deficiency from birth prevents age-related alterations in the B lineage J.

2011

Doron Melamed, PhD
Authors : Keren Z, Averbuch D, Shahaf G, Zisman-Rozen S, Golan K, Itkin T, Lapidot T, Mehr R, Melamed D.
Immunol 187, 2140 – 2147.
Epigenetics in the unicellular parasite Entamoeba histolytica.

2010

Serge Ankri, PhD
Authors : Tovy A, Ankri S.
Future Microbiol. 2010 Dec;5:1875-84.
The MAPK/ERK and PI3K pathways additively coordinate the transcription of recombination-activating genes in B lineage cells

2010

Orly Avni, PhD
Authors : Novak R, Jacob E, Haimovich J, Avni O, Melamed D.
J Immunol. 2010 Sep 15;185(6):3239-47
A fusion protein encoding the second extracellular domain of CCR5 arrests chemokine-induced cosignaling and effectively suppresses ongoing experimental autoimmune encephalomyelitis

2010

Nathan Karin, PhD
Authors : Sapir Y, Vitenshtein A, Barsheshet Y, Zohar Y, Wildbaum G, Karin N.
J Immunol. 2010 Aug 15;185(4):2589-99.
Antigen-specific CD25- Foxp3- IFN-gamma(high) CD4+ T cells restrain the development of experimental allergic encephalomyelitis by suppressing Th17

2010

Nathan Karin, PhD
Authors : Wildbaum G, Zohar Y, Karin N.
Am J Pathol. 2010 Jun; 176(6):2764-75.
Circulating interleukin-10: association with higher mortality in systolic heart failure patients with elevated tumor necrosis factor-alpha

2010

Nitza Lahat, PhD
Authors : Amir O, Rogowski O, David M, Lahat N, Wolff R, Lewis BS.
Isr Med Assoc J. 2010 Mar;12(3):158-62.
In vitro tRNA Methylation Assay with the Entamoeba histolytica DNA and tRNA Methyltransferase Dnmt2 (Ehmeth) Enzyme

2010

Serge Ankri, PhD
Authors : Tovy A, Hofmann B, Helm M, Ankri S.
J Vis Exp. 2010 Oct 19;(44). pii: 2390. doi: 10.3791/2390.
Circulating interleukin-10: association with higher mortality in systolic heart failure patients with elevated tumor necrosis factor-alpha

2010

Nitza Lahat, PhD
Authors : Amir O, Rogowski O, David M, Lahat N, Wolff R, Lewis BS
Isr Med Assoc J. 2010 Mar;12(3):158-62
A distinct mechanism for the ABC transporter BtuCD-BtuF revealed by the dynamics of complex formation.

2010

Oded Lewinson, PhD
Authors : Lewinson O, Lee AT, Locher KP, Rees DC.
Nat Struct Mol Biol. 17, 332-8.
Extracting Cell-Type-Specific Gene Expression Differences from Complex Tissues.

2010

Shai Shen-Orr, PhD
Authors : Shen-Orr SS*, Tibshirani R*, Khatri P, Bodian DL, Staedtler F, Perry NM, Hastie T, Sarwal MM, Davis MM*, Butte AJ*.
Nature Methods 7, 287-9.
The MAPK/ERK and PI(3)K Pathways Additively Coordinate the Transcription of Recombination-Activating Genes in B Lineage Cells.

2010

Doron Melamed, PhD
Authors : Novak R, Jacob E, Haimovich J, Avni O, Melamed D.
Immunol 185, 3239 – 3247.
Protein denitrosylation: enzymatic mechanisms and cellular functions

2009

Moran Benhar, PhD
Authors : Benhar, M., Forrester, M.T., Stamler, J.S.
Nat. Rev. Mol. Cell Biol. 10:721-32.
Psoriasis patients generate increased serum levels of autoantibodies to tumor necrosis factor-alpha and interferon-alpha

2009

Nathan Karin, PhD
Authors : Bergman R, Ramon M, Wildbaum G, Avitan-Hersh E, Mayer E, Shemer A, Karin N.
J Dermatol Sci. 2009 Oct 1. Epub
The role of macrophage-derived IL-1 in induction and maintenance of angiogenesis

2009

Nitza Lahat, PhD
Authors : Carmi Y, Voronov E, Dotan S, Lahat N, Rahat MA, Fogel M, Huszar M, White MR, Dinarello CA, Apte RN.
J Immunol. 2009 Oct 1;183(7):4705-14.
Insights into the mechanism of DNA recognition by the methylated LINE binding protein EhMLBP of Entamoeba histolytica

2009

Serge Ankri, PhD
Authors : Lavi T, Siman-Tov R, Ankri S.
Mol Biochem Parasitol. 2009 Aug;166(2):117-25. Epub 2009 Mar 20.
A novel recombinant fusion protein encoding a 20-amino acid residue of the third extracellular (E3) domain of CCR2 neutralizes the biological activity of CCL2

2009

Nathan Karin, PhD
Authors : Izhak L, Wildbaum G, Zohar Y, Anunu R, Klapper L, Elkeles A, Seagal J, Yefenof E, Ayalon-Soffer M, Karin N
J Immunol. 2009 Jul 1;183(1):732-9
Selective autoantibody production against CCL3‭ ‬is associated with human type 1‭ ‬diabetes mellitus and serves as a novel biomarker for its diagnosis

2009

Nathan Karin, PhD
Authors : Shehadeh N‭, ‬Pollack S‭, ‬Wildbaum G‭, ‬Zohar Y‭, ‬Shafat I‭, ‬Makhoul R‭, ‬Daod E‭,‬
J Immunol‭. ‬2009‭ ‬Jun 15‭;‬182‭(‬12‭):‬8104-9
The effect of 100% oxygen on intestinal preservation and recovery following ischemia-reperfusion injury in rats

2009

Nitza Lahat, PhD
Authors : Sukhotnik I, Brod V, Lurie M, Rahat MA, Shnizer S, Lahat N, Mogilner JG, Bitterman H.
Crit Care Med. 2009 Mar;37(3):1054-61.
Transcriptional regulation of GATA3 in T helper cells by the integrated activities of transcription factors downstream of the interleukin-4 receptor and T cell receptor

2009

Orly Avni, PhD
Authors : Scheinman EJ, Avni O.
J Biol Chem. 2009 30;284(5):3037-48.
TOLL-like receptor ligands stimulate aberrant class switch recombination in early B cell precursors

2008

Doron Melamed, PhD
Authors : Edry E, Azulay-Debby H, Melamed D.
Int Immunol. 2008 Dec;20(12):1575-85. Epub 2008 Oct 29.
EhMLBP is an essential constituent of the Entamoeba histolytica epigenetic machinery and a potential drug target

2008

Serge Ankri, PhD
Authors : Lavi T, Siman-Tov R, Ankri S.
Mol Microbiol. 2008 Jul;69(1):55-66. Epub 2008 May 12
Hypoxia enhances lysosomal TNF-α degradation in mouse peritoneal macrophages

2008

Nitza Lahat, PhD
Authors : Lahat, N., Rahat, M. A., Kinarty, A., Weiss-Cerem, L., Pinchevski, S., Bitterman, H.
Am J Physiol Cell Physiol 295, C2-12.
What do unicellular organisms teach us about DNA methylation?

2008

Serge Ankri, PhD
Authors : Harony H
Trends Parasitol. 2008 May;24(5):205-9. Epub 2008 Apr 9. PMID: 18403268 [PubMed – in process]
Regulated protein denitrosylation by cytosolic and mitochondrial thioredoxins

2008

Moran Benhar, PhD
Authors : Benhar, M., Forrester, M.T., Hess, D.T., Stamler, J.S.
Science 320:1050-4
Trichostatin A regulates peroxiredoxin expression and virulence of the parasite Entamoeba histolytica.

2008

Serge Ankri, PhD
Authors : Isakov E, Siman-Tov R, Weber C, Guillen N
Mol Biochem Parasitol. 2008 Mar;158(1):82-94.
Progress and prospects of gene inactivation in Entamoeba histolytica.

2008

Serge Ankri, PhD
Authors : Abed M
Exp Parasitol. 2008 Feb;118(2):151-5
Class switch recombination: a friend and a foe.

2007

Doron Melamed, PhD
Authors : Edry E.
Clin Immunol. 2007 Jun;123(3):244-51.
Native and fragmented fibronectin oppositely modulate monocyte secretion of MMP-9

2007

Nitza Lahat, PhD
Authors : Marom, B., Rahat, M. A., Lahat, N., Weiss-Cerem, L., Kinarty, A., Bitterman, H.
J Leukoc Biol 81, 1466-1476.
SLP-76 mediates and maintains activation of the Tec family kinase ITK via the T cell antigen receptor-induced association between SLP-76 and ITK.

2007

Deborah Yablonski, PhD
Authors : Bogin Y, Ainey C, Beach D
Proc Natl Acad Sci U S A. 2007 Apr 17;104(16):6638-43.
Dual role of SLP-76 in mediating T cell receptor-induced activation of phospholipase C-gamma1.

2007

Deborah Yablonski, PhD
Authors : Beach D, Gonen R, Bogin Y, Reischl IG
J Biol Chem. 2007 Feb 2;282(5):2937-46. Epub 2006 Dec 4.
B cell receptor editing in tolerance and autoimmunity.

2007

Doron Melamed, PhD
Authors : Azulay-Debby H.
Front Biosci. 2007 Jan 1;12:2136-47.
Genome-wide analysis of mRNA polysomal profiles with spotted DNA microarrays.

2007

Doron Melamed, PhD
Authors : Arava Y.
Methods Enzymol. 2007;431:177-201
Coadministration of plasmid DNA constructs encoding an encephalitogenic determinant and IL-10 elicits regulatory T cell-mediated protective immunity in the central nervous system.

2006

Nathan Karin, PhD
Authors : Schif-Zuck S, Wildbaum G, Karin N.
J Immunol. 2006 Dec 1;177(11):8241-7.
Sensing DNA methylation in the protozoan parasite Entamoeba histolytica.

2006

Serge Ankri, PhD
Authors : Lavi T, Isakov E, Harony H, Fisher O, Siman-Tov R.
Mol Microbiol. 2006 Dec;62(5):1373-86.
Modulation of matrix metalloproteinase-9 (MMP-9) secretion in B lymphopoiesis.

2006

Doron Melamed, PhD
Authors : Melamed D, Messika O, Glass-Marmor L, Miller A.
Int Immunol. 2006 Sep;18(9):1355-62.
A Pak- and Pix-dependent branch of the SDF-1alpha signalling pathway mediates T cell chemotaxis across restrictive barriers.

2006

Deborah Yablonski, PhD
Authors : Volinsky N, Gantman A, Yablonski D.
Biochem J. 2006 Jul 1;397(1):213-22. PMID: 16515536 [PubMed – in process]
DNA methylation and targeting of LINE retrotransposons in Entamoeba histolytica and Entamoeba invadens.

2006

Serge Ankri, PhD
Authors : Harony H, Bernes S, Siman-Tov R, Ankri S.
Mol Biochem Parasitol. 2006 May;147(1):55-63. Epub 2006 Feb 23. PMID: 16530279 [PubMed � in process]
Pleiotropic phenotype in Entamoeba histolytica overexpressing DNA methyltransferase (Ehmeth).

2006

Serge Ankri, PhD
Authors : Fisher O, Siman-Tov R, Ankri S.
Mol Biochem Parasitol. 2006 May;147(1):48-54. Epub 2006 Feb 9. PMID: 16497397 [PubMed � in process]
Hypoxia reduces the output of matrix metalloproteinase-9 (MMP-9) in monocytes by inhibiting its secretion and elevating membranal association

2006

Nitza Lahat, PhD
Authors : Rahat, M. A., Marom, B., Bitterman, H., Weiss-Cerem, L., Kinarty, A., Lahat, N.
J Leukoc Biol 79, 706-718.
Antisense inhibition of Entamoeba histolytica cysteine proteases inhibits colonic mucus degradation

2006

Serge Ankri, PhD
Authors : Moncada D, Keller K, Ankri S, Mirelman D, Chadee K.
Gastroenterology. 2006 Mar;130(3):721-30. PMID: 16530514 [PubMed � indexed for MEDLINE]
Beneficial autoimmunity participates in the regulation of rheumatoid arthritis.

2006

Nathan Karin, PhD
Authors : Zohar Y, Wildbaum G, Karin N.
Front Biosci. 2006 Jan 1;11:368-79. Review. PMID: 16146738 [PubMed – indexed for MEDLINE]
The RNA polymerase II subunit Rpb4p mediates decay of a specific class of mRNAs.

2005

Doron Melamed, PhD
Authors : Lotan R, Bar-On VG, Harel-Sharvit L, Duek L, Melamed D, Choder M.
Genes Dev. 2005 Dec 15;19(24):3004-16. PMID: 16357218 [PubMed – indexed for MEDLINE]
Single point mutations in the zinc finger motifs of the human immunodeficiency virus type 1 nucleocapsid alter RNA binding specificities of the gag protein and enhance packaging and infectivity.

2005

Doron Melamed, PhD
Authors : Mark-Danieli M, Laham N, Kenan-Eichler M, Castiel A, Melamed D, Landau M, Bouvier NM, Evans MJ, Bacharach E.
J Virol. 2005 Jun;79(12):7756-67. PMID: 15919928 [PubMed – indexed for MEDLINE]
Molecular characterization of Entamoeba histolytica Rnase III and AGO2, two RNA interference hallmark proteins.

2005

Serge Ankri, PhD
Authors : Abed M, Ankri S.
Exp Parasitol. 2005 Jul;110(3):265-9. Epub 2005 Apr 7. PMID: 15955322 [PubMed � indexed for MEDLINE]
Targeted overexpression of IL-18 binding protein at the central nervous system overrides flexibility in functional polarization of antigen-specific Th2 cells.

2005

Nathan Karin, PhD
Authors : Schif-Zuck S, Westermann J, Netzer N, Zohar Y, Meiron M, Wildbaum G, Karin N.
Immunol. 2005 Apr 1;174(7):4307-15. PMID: 15778395 [PubMed – indexed for MEDLINE]
T cell receptor-induced activation of phospholipase C-gamma1 depends on a sequence-independent function of the P-I region of SLP-76.

2005

Deborah Yablonski, PhD
Authors : Gonen R, Beach D, Ainey C, Yablonski D.
J Biol Chem. 2005 Mar 4;280(9):8364-70. Epub 2004 Dec 28. PMID: 15623534 [PubMed – indexed for MEDLINE]
Naive, effector, and memory T lymphocytes efficiently scan dendritic cells in vivo: contact frequency in T cell zones of secondary lymphoid organs does not depend on LFA-1 expression and facilitates

2005

Nathan Karin, PhD
Authors : Westermann J, Bode U, Sahle A, Speck U, Karin N, Bell EB, Kalies K, Gebert A.
J Immunol. 2005 Mar 1;174(5):2517-24. PMID: 15728457 [PubMed – indexed for MEDLINE]
Antigen receptor signaling competence and the determination of B cell fate in B-lymphopoiesis.

2005

Doron Melamed, PhD
Authors : Keren Z, Melamed D.
Histol Histopathol. 2005 Jan;20(1):187-96. Review. PMID: 15578437 [PubMed – indexed for MEDLINE]
CD19 regulates positive selection and maturation in B lymphopoiesis: lack of CD19 imposes developmental arrest of immature B cells and consequential stimulation of receptor editing.

2005

Doron Melamed, PhD
Authors : Diamant E, Keren Z, Melamed D.
Blood ;105:3247-3254.
Entamoeba histolytica DNA methyltransferase (Ehmeth) is a nuclear matrix protein that binds EhMRS2, a DNA that includes a scaffold/matrix attachment region (S/MAR).

2005

Serge Ankri, PhD
Authors : Banerjee S, Fisher O, Lohia A, Ankri S.
Mol Biochem Parasitol. 2005 Jan;139(1):91-7. PMID: 15610823 [PubMed � indexed for MEDLINE]
Epigenetic and classical activation of Entamoeba histolytica heat shock protein 100 (EHsp100) expression.

2005

Serge Ankri, PhD
Authors : Bernes S, Siman-Tov R, Ankri S.
FEBS Lett;579:6395-6402.
T cell receptor-induced activation of phospholipase C-γ1 depends on a sequence-independent function of the P-I region of SLP-76.

2005

Deborah Yablonski, PhD
Authors : Gonen R, Beach D, Ainey C, Yablonski D.
J Biol Chem ;280:8364-8370.
Characterization of cytosine methylated regions and 5-cytosine DNA methyltransferase (Ehmeth) in the protozoan parasite Entamoeba histolytica.

2004

Serge Ankri, PhD
Authors : Fisher O, Siman-Tov R, Ankri S.
Nucleic Acids Res ;1:287-297.
Modification of ligandindependent B cell receptor tonic signals activates receptor editing in immature B lymphocytes.

2004

Doron Melamed, PhD
Authors : Keren Z, Diamant E, Ostrovsky O, Bengal E, Melamed D.
J Biol Chem ;279:13418-13424.
A failsafe mechanism for negative selection of isotype-switched B cell precursors is regulated by the Fas/FasL pathway

2003

Doron Melamed, PhD
Authors : Seagal J, Edry E, Keren Z, Leider N, Benny O, Machluf M, Melamed D.
J Exp Med ;198:1609-1619.
Beneficial autoimmunity to proinflammatory mediators restrains the consequences of self-destructive immunity.

2003

Nathan Karin, PhD
Authors : Wildbaum G, Nahir MA, Karin N.
Immunity;19:679-688.
T(H) cell differentiation is accompanied by dynamic changes in histone acetylation of cytokine genes.

2002

Orly Avni, PhD
Authors : Avni O, Lee D, Macian F, Szabo SJ, Glimcher LH, Rao A.
Nat Immunol ;3:643-651.
Tr1 cell-dependent active tolerance blunts the pathogenic effects of determinant spreading.

2002

Nathan Karin, PhD
Authors : Wildbaum G, Netzer N, Karin N.
J Clin Invest ;110:701-710.
A PAK1-PIX-PKL complex is activated by the T-cell receptor independent of Nck, Slp-76 and LAT.

2001

Deborah Yablonski, PhD
Authors : Ku GM, Yablonski D, Manser E, Lim L, Weiss A.
EMBO Journal ;20:457-465.
Identification of a phospholipase C-γ1 (PLC- γ1) SH3 domain-binding site in SLP-76 required for T-cell receptor-mediated activation of PLC-γ1 and NFAT

2001

Deborah Yablonski, PhD
Authors : Yablonski D, Kadlecek T, Weiss A.
Mol Cell Biol ;21:4208-4218.
C-C chemokineencoding DNA vaccines enhance breakdown of tolerance to their gene products and treat ongoing adjuvant arthritis.

2000

Nathan Karin, PhD
Authors : Youssef S, Maor G, Wildbaum G, Grabie N, Gour-Lavie A, Karin N.
J Clin Invest ;106:361-371.
Cell-type-restricted binding of the transcription factor NFAT to a distal IL-4 enhancer in vivo.

2000

Orly Avni, PhD
Authors : Agarwal S, Avni O, Rao A.
Immunity ;12:643-652.
T cell differentiation: a mechanistic view.

2000

Orly Avni, PhD
Authors : Avni O, Rao A.
Curr Opin Immunol; 12:654-659.
A systemic cytokine response defect stratifies older adults into distinct immune profiles.

1900

Shai Shen-Orr, PhD
Authors : Shen-Orr SS*, Furman D*, Kidd BA, Morgan A, Lovelace P, Rosenberg-Hasson Y, Maecker H, Mackey S, Dekker C, Butte AJ, Davis MM.
Submitted.

 

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A Profile of a Notable Oncologist: Dr. Jeanette Wood appointed as Chief Scientific Officer at Genkyotex

 

Reporter: Aviva Lev-Ari, PhD, RN

 

Genkyotex Announces New Senior Management and Board Appointments

May 19, 2014 03:00 AM Eastern Daylight Time

GENEVA & ARCHAMPS, France–(BUSINESS WIRE)–

Genkyotex, the leading developer of selective NOX enzyme inhibitors, announced today the appointment of Dr. Jeanette Wood as Chief Scientific Officer and Dr. Joseph McCracken to the Board of Directors.

“Joe is a very welcome addition to the Board. His extensive global partnering expertise is a great asset, particularly when we look to the future of GKT137831 after Phase 2 and leveraging our NOX inhibitor technology platform to potential partners.”

A Profile of a Notable Oncologist

Dr. Wood joins Genkyotex with more than 30 years research experience in the pharmaceutical industry, most recently at AstraZeneca. In her role as Vice President and Head of iScience, Oncology iMed, she was responsible for the oncology early discovery portfolio, which consisted mostly of small molecule candidates, and leading the biology, chemistry and DMPK functions, which support both the research and development portfolios.

Before joining AstraZeneca, Dr. Wood was Head of Biology at oncology company S*BIO Pte Ltd in Singapore.

For more than 11 years, Dr. Wood worked in the oncology unit of Novartis developing expertise and a portfolio based on angiogenesis.

Her industry career started in the cardiovascular group at Ciba-Geigy, where as Hypertension Group Leader she led the team that played a major role in the discovery and development of the angiotensin II receptor antagonist valsartan (DIOVAN) and the renin inhibitor aliskiren (TEKTURNA).

Dr. Wood earned her PhD in pharmacology from the University of Otago (Dunedin, New Zealand).

“These appointments bring a wealth of experience to our management team and Board. Jeanette has a strong track record in developing new drugs through early stages of R&D. She joins Genkyotex at a perfect time as we are looking to advance novel NOX inhibitors further into development to add to our maturing pipeline of drug candidates led by GKT137831, in Phase 2 for diabetic nephropathy,” said Dr. Ursula Ney, CEO of Genkyotex. “Joe is a very welcome addition to the Board. His extensive global partnering expertise is a great asset, particularly when we look to the future of GKT137831 after Phase 2 and leveraging our NOX inhibitor technology platform to potential partners.”

Dr. Joe McCracken has more than 25 years of experience in technical, business development and market development roles with biotechnology and pharmaceutical companies. Most recently he was Global Head for Business Development & Licensing at Roche Pharma, where he was responsible for Roche Pharma’s global in-licensing and out-licensing activities. Prior to Roche Pharma, Dr. McCracken held the position of Vice President, Business Development at Genentech for more than 10 years. He was also at one time Director of Business Development and Representative Director of Genentech Ltd., Genentech’s wholly owned subsidiary in Japan, and has also held the positions of President of Technology Licensing and Alliances at Aventis, and Vice President of Worldwide Business and Technology Development at Rhone-Poulenc Rorer S.A.

Dr. McCracken holds a BSc in Microbiology, a MSc in Pharmacology and a Doctorate of Veterinary Medicine from The Ohio State University (Columbus, Ohio, USA).

About Genkyotex

Genkyotex is developing first in class, small molecule therapeutics that specifically and selectively inhibit the NOX family of enzymes. Using a unique screening platform, Genkyotex has identified novel NOX inhibitors with the potential to treat disease areas with a high clinical need and large market potential. The company’s lead product, GKT137831, is now in a Phase 2 clinical study in patients with diabetic nephropathy and has shown promise in several other disease models, including atherosclerosis, lung and liver fibrosis, osteoporosis, and in models of angiogenesis.

Early Funding of R&D:

Genkyotex was founded in 2006 by scientists from Switzerland, the USA and Japan, with backing from Geneva incubator Eclosion.

Mezzanine Funding:

Since 2011, expansion of the investor base, led by

  • Edmond de Rothschild Investment Partners, with
  • Vesalius BioCapital and
  • MP Healthcare Venture Management,

has provided significant investment to Genkyotex. Further information can be found at: www.genkyotex.com.

 

Contacts

Genkyotex
Dr. Ursula Ney, CEO
Tel: +41 22 880 1025
Mo: +44 7900 898 708
Email: ursula.ney@genkyotex.com
or
Halsin Partners
Mike Sinclair
Tel: +44 20 7318 2955
Mo: +44 7968 022075
Email: msinclair@halsin.com

 

SOURCES

http://www.businesswire.com/news/home/20140519005106/en/Genkyotex-Announces-Senior-Management-Board-Appointments#.U3t2Wxy7Rwh

On 5/19/14 5:37 PM, “info@newmedinc.com” <info@newmedinc.com> wrote:

http://www.businesswire.com/news/home/20140519005106/en/Genkyotex-Announces-Senior-Management-Board-Appointments#.U3p5gkTDcb0.email

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