Thursday, September 27, 2012

SciBX: Science-Business eXchange Contents: September 27 2012, Volume 5 / Issue 38

SciBX: Science-Business eXchange

TABLE OF CONTENTS

September 27 2012, Volume 5 / Issue 38

Analysis

Cover Story
Targets and Mechanisms
Tools

The Distillery: Therapeutics

Cancer
Cardiovascular disease
Endocrine/metabolic disease
Hepatic disease
Infectious disease
Other

The Distillery: Techniques

Disease models
Drug delivery
Markers
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Analysis

Cover Story

Top

Resetting the clock in diabetes
Lev Osherovich
doi:10.1038/scibx.2012.995
A Columbia University team has evidence that pancreatic islet β cells do not die but rather dedifferentiate in mouse models of type 1 and type 2 diabetes. The findings suggest a therapeutic strategy of reawakening these dormant cells to restore insulin secretion in diabetics.
Full Text | PDF

Targets and Mechanisms

Top

Suppressing AML through SIRPA
Kai-Jye Lou
doi:10.1038/scibx.2012.996
Toronto researchers have shown that targeting SIRPA disrupts its interaction with CD47 on macrophages and could help prevent engraftment of AML stem cells. The data provide validation for a SIRPA-Fc fusion protein being developed by Trillium that antagonizes the SIRPA-CD47 interaction.
Full Text | PDF

Tools

Top

Humanizing malaria mice
Tim Fulmer
doi:10.1038/scibx.2012.997
U.S. researchers have developed the first mouse model that recapitulates the human stages of the malarial parasite Plasmodium falciparum life cycle. The academics plan to make additional modifications to the mice to improve their utility. Pharmas already want to use the animals in early stage research.
Full Text | PDF

Slipping therapeutics to the mitochondria
Tracey Baas
doi:10.1038/scibx.2012.998
University of Georgia researchers have developed a polymeric nanoparticle technology that can selectively deliver small molecules to the mitochondria of cultured cells. The researchers are evaluating the nanoparticles in animal models of Alzheimer's disease, cancer and metabolic disorders.
Full Text | PDF

Distillery: Therapeutics

Cancer

Top

FMS-like tyrosine kinase 3 (FLT3; CD135)
doi:10.1038/scibx.2012.999
In vitro and mouse studies suggest statins could help treat FLT3-mutant AML.
Full Text | PDF

Cyclin dependent kinase 4 (CDK4); MEK; neuroblastoma Ras viral (v-Ras) oncogene (NRAS)
doi:10.1038/scibx.2012.1000
Mouse studies suggest combined inhibition of CDK4 and MEK could help treat NRAS-mutant melanomas.
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Insulin-like growth factor-1 receptor (IGF1R; CD221); insulin-like growth factor-1 (IGF-1)
doi:10.1038/scibx.2012.1001
In vitro and mouse studies suggest antagonizing IGF1R could help prevent resistance to Velcade bortezomib in patients with MM.
Full Text | PDF

Nicotinamide phosphoribosyltransferase (NAMPT)
doi:10.1038/scibx.2012.1002
Cell culture and mouse studies suggest inhibiting NAMPT could help treat MM.
Full Text | PDF

Cardiovascular disease

Top

Polyphosphate
doi:10.1038/scibx.2012.1003
In vitro and mouse studies identified inhibitors of polyphosphate that could help prevent thrombosis.
Full Text | PDF

Endocrine/metabolic disease

Top

MicroRNA-378 (miR-378); miR-378*
doi:10.1038/scibx.2012.1004
Mouse studies suggest inhibiting miR-378 could help prevent obesity and metabolic syndrome.
Full Text | PDF

PTEN (MMAC1; TEP1)
doi:10.1038/scibx.2012.1005
Human studies suggest PTEN mutations could help predict obesity risk.
Full Text | PDF

Hepatic disease

Top

IL-1 receptor (IL-1R); IL-1 receptor antagonist (IL-1RA)
doi:10.1038/scibx.2012.1006
Mouse studies suggest IL-1RA could help treat alcoholic liver disease.
Full Text | PDF

Infectious disease

Top

Dihydrofolate reductase (DHFR); pteridine reductase (PTR1)
doi:10.1038/scibx.2012.1007
Cell culture studies identified piperidine-pteridine–based PTR1 inhibitors that could help circumvent antifolate drug resistance associated with Leishmania infection.
Full Text | PDF

Granulocyte macrophage colony-stimulating factor (GM-CSF; CSF2)
doi:10.1038/scibx.2012.1008
Mouse studies suggest increasing GM-CSF signaling in airway epithelial cells could help promote recovery from influenza virus infection.
Full Text | PDF

Influenza A virus hemagglutinin (HA)
doi:10.1038/scibx.2012.1009
In vitro and mouse studies suggest the HA-targeting mAb CO5 could help prevent or treat influenza infection.
Full Text | PDF

Unknown
doi:10.1038/scibx.2012.1010
In vitro studies suggest a modified oxyphenbutazone (OPB) could help treat tuberculosis.
Full Text | PDF

Other

Top

Not applicable
doi:10.1038/scibx.2012.1011
Gerbil studies suggest stem cell–based therapy could help treat hearing loss caused by auditory neuropathy.
Full Text | PDF

Distillery: Techniques

Disease models

Top

Cystic fibrosis transmembrane conductance regulator (CFTR) knockout ferrets as models for cystic fibrosis–related diabetes
doi:10.1038/scibx.2012.1012
Cftr knockout ferrets could be useful models for cystic fibrosis–related diabetes.
Full Text | PDF

Dedifferentiation and restoration of islet β cells in diabetes
doi:10.1038/scibx.2012.1013
Diabetic mice show dedifferentiation of pancreatic islet β cells and could be used to screen compounds to restore islet β cells.
Full Text | PDF

Dj-1(Park7)-deficient mice as models for Parkinson's disease (PD)-associated neurodegeneration
doi:10.1038/scibx.2012.1014
Dj-1-deficient mice could be useful models for PD.
Full Text | PDF

Humanized mouse model for liver-stage malaria infection
doi:10.1038/scibx.2012.1015
Mice with humanized livers could be useful for identifying compounds that target the liver stage of human malarial strain Plasmodium falciparum.
Full Text | PDF

Drug delivery

Top

Activation of sphingosine 1-phosphate receptor to improve drug delivery across the blood brain barrier (BBB)
doi:10.1038/scibx.2012.1016
Sphingosine 1-phosphate receptor agonists could help improve drug delivery across the BBB.
Full Text | PDF

Mixed mitochondria-targeted polymeric nanoparticles for drug delivery
doi:10.1038/scibx.2012.1017
Nanoparticles consisting of a mix of polymeric molecules could help improve drug delivery to the mitochondria.
Full Text | PDF

Markers

Top

Markers of squamous cell lung cancer
doi:10.1038/scibx.2012.1018
Genomic studies have identified recurrent mutations in squamous cell lung cancer samples that could be useful markers or therapeutic targets.
Full Text | PDF

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