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.
Crafting cancer combinations Joanne Kotz doi:10.1038/scibx.2012.617 Two groups have developed platforms that could improve the identification of cancer drug combinations. A UNC team is using chemical proteomics to rationally design kinase inhibitor combinations that block resistance pathways, whereas MIT researchers are screening for combinations that are synergistic when dosed sequentially. Full Text | PDF
β testing adenosine receptor agonists Tim Fulmer doi:10.1038/scibx.2012.618 UCSF researchers have used a zebrafish screen to identify an adenosine receptor agonist that improved both β cell regeneration and glucose control in diabetic mice. The discovery could open up a new indication for a class of compounds that until now have been developed mainly for inflammatory and cardiovascular disorders. Full Text | PDF
Vaccines revisited Tracey Baas doi:10.1038/scibx.2012.619 An Oregon Health & Science University and Najít team has shown that hydrogen peroxide could be a better way to inactivate viral vaccines than conventional methods. Najít hopes to start a Phase I trial of an inactivated yellow fever virus vaccine in a few years. Full Text | PDF
Sequencing MRD Lauren Martz doi:10.1038/scibx.2012.620 Fred Hutchinson researchers have developed a high throughput sequencing platform to detect minimal residual disease in patients with T cell acute lymphoblastic leukemia. The team has spun out Adaptive Biotechnologies Corp. to develop the technology. Full Text | PDF
MicroRNA-23b (miR-23b) doi:10.1038/scibx.2012.621 Patient sample and mouse studies suggest agonizing miR-23b could help treat autoimmune diseases such as lupus, RA and MS. Full Text | PDF
Inducible nitric oxide synthase 2 (NOS2; iNOS); epidermal growth factor receptor variant III (EGFRvIII) doi:10.1038/scibx.2012.622 In vitro and mouse studies suggest iNOS inhibitors could help treat EGFRvIII-positive gliomas. Full Text | PDF
Unknown doi:10.1038/scibx.2012.623 Cell culture studies suggest the lipid 2-hydroxyoleate (2OHOA) could help treat glioma. Full Text | PDF
Dopamine receptor doi:10.1038/scibx.2012.624 Patient sample and cell culture studies suggest the dopamine receptor antagonist thioridazine could help treat cancer. Full Text | PDF
Proline dehydrogenase 1 (PRODH; POX) doi:10.1038/scibx.2012.625 Mouse and cell culture studies suggest inhibiting PRODH could help treat hypoxia-driven tumors. Full Text | PDF
EPH receptor A2 (EPHA2) doi:10.1038/scibx.2012.626 In vitro studies suggest EPHA2 could help prevent KS caused by KS-associated herpes virus (KSHV) infection. Full Text | PDF
Leukocyte immunoglobulin-like receptor subfamily B member 2 (LILRB2; LIR2) doi:10.1038/scibx.2012.627 Mouse and cell culture studies suggest inhibiting the interaction between angiopoietin-like proteins and LILRB2 could help treat leukemia. Full Text | PDF
c-Met proto-oncogene (MET; HGFR) doi:10.1038/scibx.2012.628 In vitro and mouse studies suggest inhibiting exosome secretion could help treat cancers including melanoma. Full Text | PDF
Androgen receptor (AR) doi:10.1038/scibx.2012.629 In vitro studies identified 1-(3-(2-chlorophenoxy)propyl)1H-indole-3-carbonitrile(CPIC) as an AR antagonist that could help treat prostate cancer. Full Text | PDF
Adenosine A2A receptor (ADORA2A) doi:10.1038/scibx.2012.630 Zebrafish and mouse studies suggest adenosine receptor agonists could regenerate β cells and help treat type 1 diabetes. Full Text | PDF
Apolipoprotein A-IV (APOA4) doi:10.1038/scibx.2012.631 Mouse studies suggest APOA4 could help treat type 2 diabetes. Full Text | PDF
Glucocerebrosidase (GBA; GCase) doi:10.1038/scibx.2012.632 Mouse and in vitro studies identified small molecule chaperones of GCase that could help treat Gaucher's disease. Full Text | PDF
Nuclear receptor coactivator 1 (NCOA1; SRC1) doi:10.1038/scibx.2012.633 Patient sample and mouse studies suggest inhibiting an SRC1 fragment could help treat endometriosis. Full Text | PDF
α-Glycerophosphate oxidase (glpO) doi:10.1038/scibx.2012.634 Mouse and in vitro studies suggest vaccines against glpO could help prevent pneumococcal meningitis. Full Text | PDF
Cyclophilin A (CYPA; PPIA) doi:10.1038/scibx.2012.635 Mouse studies suggest antagonizing PPIA could be useful for treating AD. Full Text | PDF
Not applicable doi:10.1038/scibx.2012.636 Mouse studies suggest transplantation of inhibitory neuronal precursors to the spinal cord could help treat neuropathic pain. Full Text | PDF
Not applicable doi:10.1038/scibx.2012.637 In vitro and mouse studies suggest the C-terminal domain of endostatin could help treat and prevent organ fibrosis. Full Text | PDF
Cell microarrays to identify drug-resistance pathways doi:10.1038/scibx.2012.638 Cell microarrays could be used to identify proteins and pathways mediating drug resistance in cancer. Full Text | PDF
Nanoparticle-mediated delivery of wortmannin doi:10.1038/scibx.2012.639 A nanoparticle formulation of the pan–phosphoinositide 3-kinase (PI3K) inhibitor wortmannin could reduce the drug's hepatotoxicity. Full Text | PDF
Deep sequencing for optimizing protein-based inhibitors of influenza A virus hemagglutinin doi:10.1038/scibx.2012.640 Deep sequencing could be useful for optimizing computationally designed protein-based inhibitors for influenza. Full Text | PDF
Engineering IgG4 mutants with reduced heterogeneity and improved thermal stability doi:10.1038/scibx.2012.641 Engineered IgG4 mutants that have reduced heterogeneity and increased thermal stability could help improve the production of IgG4-based biologics. Full Text | PDF
Low-density nanofiber scaffold to support cartilage repair doi:10.1038/scibx.2012.642 A low-density nanofiber scaffold could be useful for cartilage repair. Full Text | PDF
Synthetic staphylococcal enterotoxin B (SEB)-neutralizing antibodies to prevent toxic shock doi:10.1038/scibx.2012.643 Synthetic SEB-neutralizing antibodies could help protect against toxic shock syndrome. Full Text | PDF
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