|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
8
|
|
pubmed:dateCreated |
2006-8-2
|
|
pubmed:abstractText |
Mammalian target of rapamycin (mTOR) is a kinase that functions as a master switch between catabolic and anabolic metabolism and as such is a target for the design of anticancer agents. The most established mTOR inhibitors--rapamycin and its derivatives--showed long-lasting objective tumour responses in clinical trials, with CCI-779 being a first-in-class mTOR inhibitor that improved the survival of patients with advanced renal cell carcinoma. This heralded the beginning of extensive clinical programmes to further evaluate mTOR inhibitors in several tumour types. Here we review the clinical development of this drug class and look at future prospects for incorporating these agents into multitarget or multimodality strategies against cancer.
|
|
pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Adaptor Proteins, Signal Transducing,
http://linkedlifedata.com/resource/pubmed/chemical/Antineoplastic Agents,
http://linkedlifedata.com/resource/pubmed/chemical/EIF4EBP1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/MTOR protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/PTEN Phosphohydrolase,
http://linkedlifedata.com/resource/pubmed/chemical/Phosphatidylinositol 3-Kinases,
http://linkedlifedata.com/resource/pubmed/chemical/Phosphoproteins,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Kinase Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Kinases,
http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-akt,
http://linkedlifedata.com/resource/pubmed/chemical/TOR Serine-Threonine Kinases
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Aug
|
|
pubmed:issn |
1474-1776
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:volume |
5
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
671-88
|
|
pubmed:dateRevised |
2010-11-18
|
|
pubmed:meshHeading |
pubmed-meshheading:16883305-Adaptor Proteins, Signal Transducing,
pubmed-meshheading:16883305-Animals,
pubmed-meshheading:16883305-Antineoplastic Agents,
pubmed-meshheading:16883305-Drug Resistance, Neoplasm,
pubmed-meshheading:16883305-Epigenesis, Genetic,
pubmed-meshheading:16883305-Humans,
pubmed-meshheading:16883305-Neoplasms,
pubmed-meshheading:16883305-Neovascularization, Pathologic,
pubmed-meshheading:16883305-PTEN Phosphohydrolase,
pubmed-meshheading:16883305-Phosphatidylinositol 3-Kinases,
pubmed-meshheading:16883305-Phosphoproteins,
pubmed-meshheading:16883305-Protein Kinase Inhibitors,
pubmed-meshheading:16883305-Protein Kinases,
pubmed-meshheading:16883305-Proto-Oncogene Proteins c-akt,
pubmed-meshheading:16883305-Signal Transduction,
pubmed-meshheading:16883305-TOR Serine-Threonine Kinases
|
|
pubmed:year |
2006
|
|
pubmed:articleTitle |
Current development of mTOR inhibitors as anticancer agents.
|
|
pubmed:affiliation |
Service Inter Hospitalier de Cancrologie, Beaujon University Hospital, 100 Boulevard du General Leclerc, 92118 Clichy Cedex, France.
|
|
pubmed:publicationType |
Journal Article
|
