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PMID: 19383975 Published · epublish English Journal Article

The pharmacology of mTOR inhibition.

Science signaling ·Vol. 2 ·No. 67 ·2009-04-21 ·Pages pe24

Guertin DA, Sabatini DM

Abstract

A flurry of reports indicates that we are entering a new phase in the development of mammalian target of rapamycin (mTOR)-based therapies for oncology. Here, we summarize exciting findings regarding mTOR signaling and the outlook for mTOR inhibitors as tools to study the mTOR pathway and as drugs in the clinic.

MeSH Terms
Everolimus Humans Immunosuppressive Agents/pharmacology Mechanistic Target of Rapamycin Complex 1 Models, Biological Multiprotein Complexes Phosphatidylinositol 3-Kinases/metabolism Protein Binding/drug effects Protein Kinase Inhibitors/pharmacology Protein Kinases/metabolism Proteins Signal Transduction/drug effects Sirolimus/analogs & derivatives,pharmacology TOR Serine-Threonine Kinases Tacrolimus Binding Protein 1A/metabolism Transcription Factors/metabolism
Chemicals
CRTC2 protein, human Immunosuppressive Agents Multiprotein Complexes Protein Kinase Inhibitors Proteins Transcription Factors ridaforolimus temsirolimus Everolimus Protein Kinases MTOR protein, human Mechanistic Target of Rapamycin Complex 1 TOR Serine-Threonine Kinases Tacrolimus Binding Protein 1A Sirolimus
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Guertin David A
Whitehead Institute for Biomedical Research, Nine Cambridge Center, Cambridge, MA 02141, USA.
Sabatini David M
Article Info
Journal
Science signaling
Abbr.
Sci Signal
ISSN
1937-9145
Published
2009-04-21
Epub
2009-00-21
Pages
pe24
Language
English
Region
United States
NLM ID
101465400
Subset
IM
Grants
NCI NIH HHS · K99 CA129613-02 · United States
NCI NIH HHS · K99 CA129613 · United States
NIGMS NIH HHS · R01 GM072555 · United States
NIGMS NIH HHS · R01 GM072555-04 · United States
NCI NIH HHS · K99 CA129613-01A1 · United States
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