SciBx is a weekly publication that identifies and analyzes the most important translational research articles from over 40 journals. Find out which papers have real scientific and commercial potential, and why. Subscribe to SciBX and you won't miss the next big thing.
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. Full Text | PDF
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. Full Text | PDF
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. Full Text | PDF
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. Full Text | PDF
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. Full Text | PDF
ADP-ribosylation factor 1 (ARF1) doi:10.1038/scibx.2012.64 Mouse studies identified an ARF1 inhibitor that could help treat breast cancer. Full Text | PDF
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. Full Text | PDF
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. Full Text | PDF
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. Full Text | PDF
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. Full Text | PDF
Fibronectin 1 (FN1; FN) doi:10.1038/scibx.2012.69 Mouse studies identified an FN1-targeting antibody-drug conjugate that could help treat cancer. Full Text | PDF
Not applicable doi:10.1038/scibx.2012.70 Mouse studies suggest activating autophagy or increasing ATP release from tumor cells could help treat cancer. Full Text | PDF
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. Full Text | PDF
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. Full Text | PDF
Sphingosine 1-phosphate receptor doi:10.1038/scibx.2012.73 Studies in mice suggest that agonizing sphingosine 1-phosphate receptors could help treat diabetes. Full Text | PDF
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. Full Text | PDF
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. Full Text | PDF
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. Full Text | PDF
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). Full Text | PDF
Matrix metalloproteinase 9 (MMP9) doi:10.1038/scibx.2012.78 Mouse studies identified antibodies that inhibit MMP9 to help treat inflammatory diseases. Full Text | PDF
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. Full Text | PDF
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. Full Text | PDF
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. Full Text | PDF
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. Full Text | PDF
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. Full Text | PDF
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. Full Text | PDF
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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