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PMID: 12020063 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

Inhibitors of mammalian target of rapamycin as novel antitumor agents: from bench to clinic.

Current opinion in investigational drugs (London, England : 2000) ·Vol. 3 ·No. 2 ·2002-02-00 ·Pages 295-304

Huang S, Houghton PJ

Abstract

Rapamycin and its derivatives, CCI-779 and RAD-001, inhibit the mammalian target of rapamycin (mTOR), downregulating translation of specific mRNAs required for cell cycle progression from G1 to S phase. Preclinically, mTOR inhibitors potently suppress growth and proliferation of numerous tumor cell lines in culture or when grown in mice as xenografts. CCI-779 and RAD-001 are being developed as antitumor drugs and are undergoing clinical trials. Clinically, CCI-779 has shown evidence of antitumor activity but induced relatively mild side effects in patients. Here we discuss potential antitumor mechanisms and resistance mechanisms of mTOR inhibitors, and summarize the current status of these compounds as novel antitumor agents.

MeSH Terms
Antineoplastic Agents/pharmacology,therapeutic use Cell Division/drug effects Clinical Trials, Phase I as Topic Drug Resistance, Neoplasm/genetics Everolimus Humans Neoplasms/drug therapy Protein Kinase Inhibitors Protein Kinases/genetics Sirolimus/analogs & derivatives,pharmacology,therapeutic use TOR Serine-Threonine Kinases Treatment Outcome Tumor Cells, Cultured
Chemicals
Antineoplastic Agents Protein Kinase Inhibitors temsirolimus Everolimus Protein Kinases MTOR protein, human mTOR protein, mouse TOR Serine-Threonine Kinases Sirolimus
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Huang Shile
Department of Molecular Pharmacology, St Jude Children's Research Hospital, Memphis, TN 38105-2794, USA.
Houghton Peter J
Article Info
Journal
Current opinion in investigational drugs (London, England : 2000)
Abbr.
Curr Opin Investig Drugs
ISSN
1472-4472
Published
2002-02-00
Pages
295-304
Language
English
Region
England
NLM ID
100965718
Subset
IM
Grants
NCI NIH HHS · CA23099 · United States
NCI NIH HHS · CA28765 · United States
NCI NIH HHS · CA77776 · United States
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