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PMID: 25747336 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Targeting PTEN using small molecule inhibitors.

Methods (San Diego, Calif.) ·Vol. 77-78 ·2015-05-00 ·Pages 63-8

Mak LH, Woscholski R

Abstract

PTEN (phosphatase and tensin homologue deleted on chromosome 10) is well known as a tumour suppressor. It's PI(3,4,5)P3 lipid phosphatase activity is an important counteracting mechanism in PI 3-kinase (phosphoinositide 3-kinase) signalling. Furthermore, PTEN lies upstream of Akt kinase, a key enzyme in insulin signalling regulating glucose uptake and cell growth. Therefore, PTEN has recently gained attention as a valuable drug target for the treatment of diabetes, stroke, cardiac infarct and fertility. This review summarizes the use of small molecules as PTEN inhibitors. Currently available methodologies and techniques for accessing PTEN inhibition in vitro and in cellulo will be discussed.

Keywords
Inhibition OMFP PTEN VO-OHpic Vanadium compounds
MeSH Terms
Animals Gene Targeting/methods Humans PTEN Phosphohydrolase/analysis,genetics Phosphatidylinositol 3-Kinases/genetics Proto-Oncogene Proteins c-akt/genetics Tumor Suppressor Proteins/analysis,genetics
Chemicals
Tumor Suppressor Proteins Phosphatidylinositol 3-Kinases Proto-Oncogene Proteins c-akt PTEN Phosphohydrolase PTEN protein, human
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Mak Lok Hang
Department of Chemistry, Imperial College London, Exhibition Road, London SW7 2AZ, UK. Electronic address: lokhangmak@gmail.com.
Woscholski Rudiger
Department of Chemistry, Imperial College London, Exhibition Road, London SW7 2AZ, UK; Institute of Chemical Biology, Imperial College London, Exhibition Road, London SW7 2AZ, UK. Electronic address: r.woscholski@imperial.ac.uk.
Article Info
Journal
Methods (San Diego, Calif.)
Abbr.
Methods
ISSN
1095-9130
Published
2015-05-00
Epub
2015-00-04
Pages
63-8
Language
English
Region
United States
NLM ID
9426302
Subset
IM
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