TABLE OF CONTENTS |
June 6 2013, Volume 6 / Issue 22 |
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 | Analysis Cover Story Translational Notes Targets and Mechanisms
The Distillery: Therapeutics Cancer Cardiovascular disease Endocrine/metabolic disease Hematology Inflammation Neurology Other Pulmonary disease Transplantation
The Distillery: Techniques Disease models Drug platforms Imaging Instrumentation Markers
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Analysis |
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Cover Story | Top |
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Driving cancer through ErbB3 Kai-Jye Lou doi:10.1038/scibx.2013.535
Genentech researchers show that mutations in ERBB3 can drive oncogenesis in a process dependent on the receptor's ability to form a heterodimer with HER2. The findings suggest existing HER2-targeted therapies also could be effective against cancers driven by mutations in ERBB3.
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Translational Notes | Top |
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Not-so-fast track Lev Osherovich doi:10.1038/scibx.2013.536
GSK's Discovery Fast Track competition, which aims to establish direct collaborations with academic researchers, hit a road block when the UCLA Office of IP said that UCLA researchers cannot participate. The head of that office believes GSK is doing an end-run around traditional IP vetting by tech transfer offices and that his policy should be UC system–wide.
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Targets and Mechanisms | Top |
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Watching obesity on a new channel C. Simone Fishburn doi:10.1038/scibx.2013.537
UC-Irvine researchers have found that an inhibitor of the potassium channel Kv1.3, a known autoimmunity target, may represent a new class of therapeutic for treating obesity-related diseases. The team has licensed the inhibitor, ShK-186, to Kineta and thinks it could treat the indication via a trio of distinct mechanisms.
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Nanoparticles for the flu Tracey Baas doi:10.1038/scibx.2013.538
An NIH team has created a self-assembling influenza nanoparticle that induces the production of antibodies against a wider range of flu strains than traditional vaccines. The next step is immunogenicity testing in humans.
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Distillery: Therapeutics |
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Cancer | Top |
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Epidermal growth factor receptor 3 (EGFR3; HER3; ERBB3); HER2 (EGFR2; ErbB2; neu) doi:10.1038/scibx.2013.539
Patient sample and mouse studies identified oncogenic somatic mutations in ErbB3 that could guide the use of HER2 and ErbB3 inhibitors.
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Integrin α4β1 (CD49D/CD29) doi:10.1038/scibx.2013.540
Human and mouse studies suggest inhibiting integrin α4β1 could help prevent metastasis.
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Poliovirus receptor–related 4 (PVRL4) doi:10.1038/scibx.2013.541
In vitro and mouse studies suggest inhibiting PVRL4 could help treat cancer.
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Thrombospondin-1 (TSP-1; THBS1); prosaposin (PSAP) doi:10.1038/scibx.2013.542
Cell-based and mouse studies suggest increasing TSP-1 expression could help treat metastatic cancer.
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Tumor necrosis factor receptor 1 (TNFRSF1A; TNFR1; CD120a) doi:10.1038/scibx.2013.543
A study in mice suggests decreasing TNFRSF1A could improve the safety of tumor necrosis factor (TNF)-based cancer treatments.
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RAD51 homolog (RAD51); activation-induced cytidine deaminase (AICDA; AID) doi:10.1038/scibx.2013.544
Studies in patient-derived cells and in mice suggest antagonizing RAD51 could be useful for treating AID-expressing CLL.
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VEGF receptor 2 (KDR/Flk-1; VEGFR-2) doi:10.1038/scibx.2013.545
Mouse studies suggest co-delivery of engineered T cells expressing a chimeric antigen receptor (CAR) targeting VEGFR-2 and engineered T cells expressing tumor-specific T cell receptors (TCRs) could help treat melanoma.
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Cardiovascular disease | Top |
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Growth differentiation factor 11 (GDF11) doi:10.1038/scibx.2013.546
Studies in mice suggest GDF11 could be useful for treating age-related cardiac hypertrophy.
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Endocrine/metabolic disease | Top |
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Fatty acid binding protein 4 adipocyte (FABP4) doi:10.1038/scibx.2013.547
In vitro and mouse studies suggest blocking FABP4 could help treat diabetes.
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Hematology | Top |
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Factor VIII doi:10.1038/scibx.2013.548
Mouse studies suggest phosphatidylserine-bound factor VIII could help treat patients with hemophilia A.
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Inflammation | Top |
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Dendritic cell–specific ICAM-3 grabbing nonintegrin (DC-SIGN; CD209) doi:10.1038/scibx.2013.549
Cell culture and mouse studies identified DC-SIGN-binding mannodendrimers that could help treat inflammatory diseases.
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Neurology | Top |
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Peripheral benzodiazepine receptor (TSPO; PBR) doi:10.1038/scibx.2013.550
Mouse studies suggest TSPO ligands could be used to treat AD.
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Protocadherin 17 (PCDH17) doi:10.1038/scibx.2013.551
Mouse and nonhuman primate studies suggest inhibiting PCDH17 could help treat depression.
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Other | Top |
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Isoprenylcysteine carboxyl methyltransferase (ICMT) doi:10.1038/scibx.2013.552
Mouse and cell culture studies suggest inhibiting ICMT could help treat Hutchinson-Gilford progeria syndrome (HGPS), which causes premature aging.
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Pulmonary disease | Top |
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Cystic fibrosis transmembrane conductance regulator (CFTR) doi:10.1038/scibx.2013.553
In vitro and cell culture studies identified the molecular mechanism of action for CFTR corrector compounds and suggest new combination approaches that could help treat CF.
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Transplantation | Top |
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Tumor necrosis factor–related apoptosis-inducing ligand (TRAIL) doi:10.1038/scibx.2013.554
TRAIL-overexpressing T cells could be useful for both treating GvHD and improving antitumor immunity following a hematopoietic stem cell transplant (HSCT).
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Distillery: Techniques |
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Disease models | Top |
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Clustered, regularly interspaced short palindromic repeats (CRISPR)-based editing system for one-step production of multigene knockout mice doi:10.1038/scibx.2013.555
CRISPR-based genome editing could be used to rapidly generate mice with multiple genetic mutations.
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Modeling skeletal muscle deficits in Huntington's disease (HD) doi:10.1038/scibx.2013.556
Mouse muscle fibers could be useful for modeling HD-associated musculoskeletal deficits and could aid the development of new therapies to treat the disease.
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Mouse model for autosomal-dominant leukodystrophy (ADLD) doi:10.1038/scibx.2013.557
A mouse model for adult-onset ADLD could be useful for identifying myelin regeneration therapies to treat ADLD and multiple sclerosis (MS).
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Mouse model for partner and localizer of Brca2 (Palb2)-deficient breast cancer doi:10.1038/scibx.2013.558
A mouse model for Palb2-deficient breast cancer could be useful for evaluating new therapies.
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Drug platforms | Top |
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Direct conversion of fibroblasts to insulin-secreting cells using DNA demethylating agents doi:10.1038/scibx.2013.559
In vitro and mouse studies suggest demethylating agents could be used to directly convert adult fibroblasts into insulin-producing cells.
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Humanized shark variable new antigen receptors (VNARs) doi:10.1038/scibx.2013.560
Humanized versions of VNARs could be used to bind protein epitopes that are difficult to access using traditional antibodies.
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Imaging | Top |
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High-density lipoprotein (HDL)-mimicking nanoparticles to detect vulnerable atherosclerotic plaques doi:10.1038/scibx.2013.561
In vitro and rat studies identified synthetic, HDL-mimicking nanoparticles that could help detect vulnerable atherosclerotic plaques, which can rupture and cause fatal blood clots.
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Instrumentation | Top |
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Poly(carboxybetaine methacrylate) (PCBMA), zwitterionic hydrogels to coat implantable devices doi:10.1038/scibx.2013.562
Mouse studies identified PCBMA hydrogels that could be applied to implantable devices to prevent foreign body reactions.
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Markers | Top |
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G-CSF receptor (CSF3R; CD114) mutations to guide diagnosis and treatment of atypical chronic myelogenous leukemia (aCML) and chronic neutrophilic leukemia (CNL) doi:10.1038/scibx.2013.563
Patient sample studies suggest mutations in CD114 could help diagnose aCML and CNL and guide treatment decisions for the diseases.
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