Friday, January 13, 2012

Drug Discovery@nature.com 13 January 2012

Drug Discovery
TABLE OF CONTENTS

13 January 2012

News
Analysis
Research Highlights
Research & Reviews
Careers


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News

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Incyte comes of age with JAK inhibitor approval
doi:10.1038/nbt0112-3
Incyte's first drug to market, Jakafi (ruxolitinib), is one that validates a novel mechanism of action in cancer - blocking the Janus-kinases JAK1 and JAK2.
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Eylea approval transforms Regeneron
doi:10.1038/nbt0112-4
Regeneron's launch of Eylea (aflibercept) to treat wet age-related macular degeneration effectively changes the company from one dependent on partnering and licensing into a commercial organization.
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Rules tighten on use of antibiotics on farms
doi:10.1038/481125a
Clampdown aims to stop spread of drug-resistant microbes.
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An audience with Mark Fishman
doi:10.1038/nrd3640

Mark Fishman, President of the Novartis Institutes for BioMedical Research, looks back on his past decade of heading up R&D.
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Analysis

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No place like inflammasome
doi:10.1038/scibx.2012.1
Researchers have found that inhibiting inflammasome formation with P2X7 antagonists could help prevent heart failure following acute myocardial infarction. The findings highlight a repurposing opportunity for P2X7 antagonists that companies have in the clinic for inflammatory indications.
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Fresh from the Pipeline: Brentuximab vedotin
doi:10.1038/nrd3629
In August 2011, brentuximab vedotin (Adcetris; Seattle Genetics), a CD30-specific antibody-drug conjugate, was approved by the US Food and Drug Administration for the treatment of patients with Hodgkin's lymphoma and patients with systemic anaplastic large cell lymphoma.
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From the analyst's couch: A decade of change
doi:10.1038/nrd3630
Data on indicators such as the number and success rate of research and development projects illustrate trends in the pharmaceutical industry over the past decade.
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Research Highlights

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Vaccines: Enhancing glycan presentation increases vaccine efficacy
doi:10.1038/nrd3637
By maximizing the presentation of carbohydrate epitopes to T cells, scientists have constructed a vaccine against group B streptococcus that is significantly more potent than currently available vaccines.
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Antiparasitic drugs: Two-pronged tactics for malaria control
doi:10.1038/nrd3635
An academia–industry consortium has identified a new class of compounds that confer complete protection against parasite challenge in rodent models of malaria, as well as showing potent in vivo activity against blood-stage parasites.
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Epigenetics: Worth another look?
doi:10.1038/nrc3187
Patients with non-small-cell lung cancer with tumours that have a specific subset of methylated genes might benefit from combined treatment with a low-dose DNA methyltransferase inhibitor and a histone deacetylase inhibitor.
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Research & Reviews

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The pharmacological landscape and therapeutic potential of serine hydrolases
doi:10.1038/nrd3620
This article outlines the current state of pharmacology for mammalian serine hydrolases, including marketed drugs, compounds that are under clinical investigation and selective inhibitors emerging from academic probe development efforts.
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Cancer immunotherapy comes of age
doi:10.1038/nature10673
Advances in the understanding of how tolerance, immunity and immunosuppression regulate antitumour immune responses, together with the advent of targeted therapies, suggest that active immunotherapy represents a path to obtain a durable and long-lasting response in cancer patients.
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Topoisomerase inhibitors unsilence the dormant allele of Ube3a in neurons
doi:10.1038/nature10726
Findings from a recent Nature study suggest a therapeutic strategy for reactivating the functional but dormant allele of Ube3a in patients with Angelman syndrome using topoisomerase inhibitors.
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Antibodies targeting the catalytic zinc complex of activated matrix metalloproteinases show therapeutic potential
doi:10.1038/nm.2582
Antibodies that bind and inhibit activated matrix metalloproteinases 2 and 9 in a manner analogous to the mechanism of action of tissue inhibitors of metalloproteinases are therapeutically effective in mouse models of inflammatory bowel disease.
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Drug Discovery
JOBS of the week
Head of Structural Biology / Crystallography
H3 Biomedicine
MRes in Drug Discovery and Development
Imperial College London
Scientist, Small Molecule Discovery Toxicology (Safety Assessment)
Genentech
(Senior) Principal Scientist
Eisai Ltd
Research Investigator in Oncology
BeiGene Inc.
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Drug Discovery
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Advances and Progress in Drug Design
21.-22.01.12
London, UK
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Careers

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Career snapshots archive
Career snapshots feature people associated with drug discovery and drug development, with the aim of providing expert insights and advice on a wide range of positions and career paths in this field.
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