Thursday, January 19, 2012

SciBX: Science-Business eXchange Contents: January 19 2012, Volume 5/ Issue 3

SciBX: Science-Business eXchange

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TABLE OF CONTENTS

January 19 2012, Volume 5 / Issue 3

Analysis

Cover Story
Translational Notes
Targets and Mechanisms

The Distillery: Therapeutics

Autoimmune disease
Cancer
Endocrine/metabolic disease
Hematology
Infectious disease
Inflammation
Neurology
Other
Transplantation
Various

The Distillery: Techniques

Disease models
Drug platforms
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Analysis

Cover Story

Top

Spreadin' the news
Kai-Jye Lou
doi:10.1038/scibx.2012.59
SciBX's roundup of 2011 public-private partnership data shows the emergence of New York as a translational hub, the impact of nongovernmental funding on infectious disease research compared with the more muted VC support of this area, and the high interest of foreign companies in funding research in China.
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Translational Notes

Top

Seeing the (En)light
Chris Cain
doi:10.1038/scibx.2012.60
AstraZeneca and Novo Nordisk have come off the sidelines to partner with Enlight Biosciences, making them the sixth and seventh pharmas currently working with Enlight to form platform companies.
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Scripps' partnering rethink
Lev Osherovich
doi:10.1038/scibx.2012.61
The Scripps Research Institute has decided that the kind of broad deals it used to do with industry do not work anymore. Instead, the institute now hopes to forge a series of smaller, more focused collaborations with midsize biotechs.
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Targets and Mechanisms

Top

Heat shock and awe
Tim Fulmer
doi:10.1038/scibx.2012.62
U.S. researchers have identified several small molecules that decrease toxic protein aggregation in vitro. The first-generation compounds have been licensed by Proteostasis and are proof of concept for the biotech's approach to treating protein misfolding diseases like Huntington's and cystic fibrosis.
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Distillery: Therapeutics

Autoimmune disease

Top

Transglutaminase 2 (TGM2; TG2)
doi:10.1038/scibx.2012.63
In vitro studies identified autoantibody binding sites of TG2 that could be blocked to help treat celiac disease.
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Cancer

Top

ADP-ribosylation factor 1 (ARF1)
doi:10.1038/scibx.2012.64
Mouse studies identified an ARF1 inhibitor that could help treat breast cancer.
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Mucin 1 (MUC1; CD227)
doi:10.1038/scibx.2012.65
Mouse studies suggest an immunotherapy based on a MUC1 glycopeptide could help treat breast cancer.
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Nerve growth factor (NGF)
doi:10.1038/scibx.2012.66
Cell culture and patient tissue studies suggest pro-NGF could be antagonized to treat breast cancer.
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Taspase threonine aspartase 1 (TASP1)
doi:10.1038/scibx.2012.67
Cell culture and mouse studies identified a TASP1 inhibitor that could help treat breast cancer and gliomas.
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Checkpoint kinase 1-short (Chk1-S)
doi:10.1038/scibx.2012.68
In vitro and mouse studies suggest increasing levels of Chk1-S may help treat cancer.
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Fibronectin 1 (FN1; FN)
doi:10.1038/scibx.2012.69
Mouse studies identified an FN1-targeting antibody-drug conjugate that could help treat cancer.
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Not applicable
doi:10.1038/scibx.2012.70
Mouse studies suggest activating autophagy or increasing ATP release from tumor cells could help treat cancer.
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Sirtuin 1 (SIRT1)
doi:10.1038/scibx.2012.71
In vitro and mouse studies suggest inhibiting SIRT1 could increase the efficacy of Gleevec imatinib in CML.
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Endocrine/metabolic disease

Top

Fibroblast growth factor receptor 1 (FGFR1; CD331); fibroblast growth factor 21 (FGF21)
doi:10.1038/scibx.2012.72
A study in mice suggests an agonist mAb of FGFR1 could help treat type 2 diabetes.
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Sphingosine 1-phosphate receptor
doi:10.1038/scibx.2012.73
Studies in mice suggest that agonizing sphingosine 1-phosphate receptors could help treat diabetes.
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Hematology

Top

CXC chemokine receptor 4 (CXCR4; NPY3R); chemokine CXC motif ligand 12 (CXCL12; SDF-1); CXCR7
doi:10.1038/scibx.2012.74
In vitro and mouse studies suggest inhibiting the CXCR4/CXCR7/SDF-1 signaling pathway could help treat or prevent hemolytic uremic syndrome following Escherichia coli infection.
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Infectious disease

Top

UDP-3-O-[3-hydroxymyristoyl] N-acetylglucosamine deacetylase (LpxC)
doi:10.1038/scibx.2012.75
In vitro and mouse studies identified hydroxamic acid–based LpxC inhibitors that could help treat Gram-negative bacterial infections.
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Niemann-Pick C1-like protein (NPC1L1)
doi:10.1038/scibx.2012.76
In vitro and mouse studies suggest NPC1L1 inhibitors could help prevent HCV infection.
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Receptor-interacting serine-threonine kinase 1 (RIPK1; RIP1); RIPK3 (RIP3)
doi:10.1038/scibx.2012.77
Mouse studies suggest that inhibition of RIPK1 and/or RIPK3 could help prevent systemic inflammatory response syndrome (SIRS).
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Inflammation

Top

Matrix metalloproteinase 9 (MMP9)
doi:10.1038/scibx.2012.78
Mouse studies identified antibodies that inhibit MMP9 to help treat inflammatory diseases.
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Neurology

Top

Nicotinic acetylcholine receptor α4β2
doi:10.1038/scibx.2012.79
In vitro and mouse studies suggest two new classes of nicotinic acetylcholine receptor α4β2 partial agonists could help treat depression.
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Heat shock transcription factor 1 (HSF1)
doi:10.1038/scibx.2012.80
An in vitro screen identified small molecule compounds that activated the heat shock response and could help treat HD and other protein misfolding diseases.
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Mitochondrial complex 1 (MC-1)
doi:10.1038/scibx.2012.81
Rat studies suggest a fusion protein consisting of the rabies virus glycoprotein (RVG) linked to a cytomegalovirus (CMV)-derived RNA sequence could help treat PD.
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Other

Top

Ryanodine receptor 1 (RyR1)
doi:10.1038/scibx.2012.82
Mouse studies suggest 5-aminoimidazole-4-carboxamide ribonucleoside (AICAR) could help prevent heat-induced sudden death caused by RyR1 mutations.
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Transplantation

Top

Haptoglobin (HP)
doi:10.1038/scibx.2012.83
Mouse studies suggest that antagonizing HP could help prevent graft rejection.
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Various

Top

p38 Mitogen-activated protein kinase (p38 MAPK; MAPK14)
doi:10.1038/scibx.2012.84
In vitro and mouse studies identified a compound that could help guide the development of selective p38 MAPK–targeted therapeutics for cancer and inflammatory diseases.
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Distillery: Techniques

Disease models

Top

Induced pluripotent stem (iPS) cell model for Timothy syndrome
doi:10.1038/scibx.2012.85
A study in cell culture suggests patient-derived iPS cells could help identify therapies for Timothy syndrome, a form of autism spectrum disorder.
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Drug platforms

Top

Isoxazole compounds for pancreatic islet b cell regeneration
doi:10.1038/scibx.2012.86
A study in cell culture suggests 3,5-disubstitute isoxazoles could be useful for regenerating islet b cells in type 1 diabetes.
Full Text | PDF

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