机构:
Hosp Mar, IMAS, Med Oncol Serv, ES-08003 Barcelona, Spain
Hosp Mar, IMIM, Expt Therapy Canc Res Unit URTEC, PRBB, Barcelona, SpainHosp Mar, IMAS, Med Oncol Serv, ES-08003 Barcelona, Spain
Albanell, J.
[1
,2
]
Dalmases, A.
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Hosp Mar, IMIM, Expt Therapy Canc Res Unit URTEC, PRBB, Barcelona, SpainHosp Mar, IMAS, Med Oncol Serv, ES-08003 Barcelona, Spain
Dalmases, A.
[2
]
Rovira, A.
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机构:
Hosp Mar, IMAS, Med Oncol Serv, ES-08003 Barcelona, Spain
Hosp Mar, IMIM, Expt Therapy Canc Res Unit URTEC, PRBB, Barcelona, SpainHosp Mar, IMAS, Med Oncol Serv, ES-08003 Barcelona, Spain
Rovira, A.
[1
,2
]
Rojo, F.
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Hosp Mar, IMIM, Expt Therapy Canc Res Unit URTEC, PRBB, Barcelona, Spain
Hosp Mar IMAS, Dept Pathol, Barcelona, SpainHosp Mar, IMAS, Med Oncol Serv, ES-08003 Barcelona, Spain
Rojo, F.
[2
,3
]
机构:
[1] Hosp Mar, IMAS, Med Oncol Serv, ES-08003 Barcelona, Spain
[2] Hosp Mar, IMIM, Expt Therapy Canc Res Unit URTEC, PRBB, Barcelona, Spain
Inhibitors of mTOR, the mammalian target of rapamycin, have been extensively studied in clinical trials for cancer treatment. Results have been promising, mostly in certain lymphomas, but in solid tumours the results have been generally less encouraging. However, recent results, particularly in renal cell carcinoma, have provided renewed interest in the role of mTOR inhibitors in solid tumours. A rational, and potentially more successful, development of these agents ( i. e., RAD001, temsirolimus and AP23573) likely relies in a deeper knowledge of mTOR signalling in cancer, both at the preclinical and clinical levels. These would allow a better selection of patients more likely to respond to the use of biologically active doses of the agents and the development of mechanistically based combinations with other agents. The goal of this review is to provide an update on the complex signalling of mTOR in cancer and on the biological effects of mTOR inhibitors in cancer cells.