Thursday, June 6, 2013

SciBX: Science-Business eXchange Contents: June 06 2013, Volume 6 / Issue 22

SciBX: Science-Business eXchange

TABLE OF CONTENTS

June 6 2013, Volume 6 / Issue 22

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
Advertisement
Biopharma Dealmakers
A supplement to Nature Biotechnology and Nature Reviews Drug Discovery

The April 2013 issue of Biopharma Dealmakers showcases companies with partnering opportunities. This week, find out about how you can collaborate with Sanford-Burnham Medical Research Institute and The Menarini Group.



Advertisement

SciBX: Science Business eXchange
Innovation in Drug Discovery Challenge:
Harnessing Endocytosis for Drug Discovery

SciBX, in partnership with Innocentive, is requesting ideas from the scientific community to progress the understanding of how large therapeutic molecules can effectively intercept and use the endocytosis process to achieve class-wide cell permeability.
 
Click here to find out more!
 
Advertisement
Nature Publishing Group and Relay Technology Management present:
The Epigenetics Target Explorer

Click here to access this free online tool and the accompanying article in Nature Reviews Drug Discovery.
 

Analysis

Cover Story

Top

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.
Full Text | PDF

Translational Notes

Top

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.
Full Text | PDF

Targets and Mechanisms

Top

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.
Full Text | PDF

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.
Full Text | PDF

Distillery: Therapeutics

Cancer

Top

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.
Full Text | PDF

Integrin α4β1 (CD49D/CD29)
doi:10.1038/scibx.2013.540
Human and mouse studies suggest inhibiting integrin α4β1 could help prevent metastasis.
Full Text | PDF

Poliovirus receptor–related 4 (PVRL4)
doi:10.1038/scibx.2013.541
In vitro and mouse studies suggest inhibiting PVRL4 could help treat cancer.
Full Text | PDF

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.
Full Text | PDF

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.
Full Text | PDF

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.
Full Text | PDF

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.
Full Text | PDF

Cardiovascular disease

Top

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.
Full Text | PDF

Endocrine/metabolic disease

Top

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.
Full Text | PDF

Hematology

Top

Factor VIII
doi:10.1038/scibx.2013.548
Mouse studies suggest phosphatidylserine-bound factor VIII could help treat patients with hemophilia A.
Full Text | PDF

Inflammation

Top

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.
Full Text | PDF

Neurology

Top

Peripheral benzodiazepine receptor (TSPO; PBR)
doi:10.1038/scibx.2013.550
Mouse studies suggest TSPO ligands could be used to treat AD.
Full Text | PDF

Protocadherin 17 (PCDH17)
doi:10.1038/scibx.2013.551
Mouse and nonhuman primate studies suggest inhibiting PCDH17 could help treat depression.
Full Text | PDF

Other

Top

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.
Full Text | PDF

Pulmonary disease

Top

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.
Full Text | PDF

Transplantation

Top

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).
Full Text | PDF

Distillery: Techniques

Disease models

Top

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.
Full Text | PDF

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.
Full Text | PDF

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).
Full Text | PDF

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.
Full Text | PDF

Drug platforms

Top

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.
Full Text | PDF

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.
Full Text | PDF

Imaging

Top

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.
Full Text | PDF

Instrumentation

Top

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.
Full Text | PDF

Markers

Top

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.
Full Text | PDF

You have been sent this Table of Contents Alert because you have opted in to receive it. You can change or discontinue your e-mail alerts at any time, by modifying your preferences on your nature.com account at: www.nature.com/myaccount
(You will need to log in to be recognised as a nature.com registrant)

For further technical assistance, please contact our registration department

For print subscription enquiries, please contact our subscription department

For other enquiries, please contact our customer feedback department

Nature Publishing Group | 75 Varick Street, 9th Floor | New York | NY 10013-1917 | USA

Nature Publishing Group's worldwide offices:
London - Paris - Munich - New Delhi - Tokyo - Melbourne
San Diego - San Francisco - Washington - New York - Boston

Macmillan Publishers Limited is a company incorporated in England and Wales under company number 785998 and whose registered office is located at Brunel Road, Houndmills, Basingstoke, Hampshire RG21 6XS.

© 2013 Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved.

nature publishing group

No comments: