MTOR signalling in human cancer

被引:50
作者
Albanell, J. [1 ,2 ]
Dalmases, A. [2 ]
Rovira, A. [1 ,2 ]
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
[3] Hosp Mar IMAS, Dept Pathol, Barcelona, Spain
关键词
mTOR; rapamycin; RAD001; temsirolimus; AP23573; P70; S6; KINASE; TUBEROUS SCLEROSIS; PHOSPHATIDYLINOSITOL; 3-KINASE; MAMMALIAN TARGET; CELL-GROWTH; PROTEIN-SYNTHESIS; MESSENGER-RNAS; BINDING DOMAIN; BREAST-CANCER; GENE TSC1;
D O I
10.1007/s12094-007-0092-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:484 / 493
页数:10
相关论文
共 112 条
[1]   Human bladder tumors with 2-hit mutations of the tumor suppressor gene TSC1 and decreased expression of p27 [J].
Adachi, H ;
Igawa, M ;
Shiina, H ;
Urakami, S ;
Shigeno, K ;
Hino, O .
JOURNAL OF UROLOGY, 2003, 170 (02) :601-604
[2]  
[Anonymous], P AM ASS CANC RES
[3]  
[Anonymous], P AM ASS CANC RES
[4]   Structure of cDNAs encoding human eukaryotic initiation factor 3 subunits - Possible roles in RNA binding and macromolecular assembly [J].
Asano, K ;
Vornlocher, HP ;
RichterCook, NJ ;
Merrick, WC ;
Hinnebusch, AG ;
Hershey, JWB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (43) :27042-27052
[5]   Activation of translation complex eIF4F is essential for the genesis and maintenance of the malignant phenotype in human mammary epithelial cells [J].
Avdulov, S ;
Li, S ;
Michalek, V ;
Burrichter, D ;
Peterson, M ;
Perlman, DM ;
Manivel, JC ;
Sonenberg, N ;
Yee, D ;
Bitterman, PB ;
Polunovsky, VA .
CANCER CELL, 2004, 5 (06) :553-563
[6]   Y box-binding protein 1 induces resistance to oncogenic transformation by the phosphatidylinositol 3-kinase pathway [J].
Bader, AG ;
Feits, KA ;
Jiang, N ;
Chang, HW ;
Vogt, PK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (21) :12384-12389
[7]   Detecting activation of ribosomal protein S6 kinase by complementary DNA and tissue microarray analysis [J].
Bärlund, M ;
Forozan, F ;
Kononen, J ;
Bubendorf, L ;
Chen, YD ;
Bittner, ML ;
Torhorst, J ;
Haas, P ;
Bucher, C ;
Sauter, G ;
Kallioniemi, OP ;
Kallioniemi, A .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2000, 92 (15) :1252-1259
[8]   Present strategies in the treatment of metastatic renal cell carcinoma: an update on molecular targeting agents [J].
Bellmunt, Joaquim ;
Montagut, Clara ;
Albiol, Santiago ;
Carles, Joan ;
Maroto, Pablo ;
Orsola, Anna .
BJU INTERNATIONAL, 2007, 99 (02) :274-280
[9]   Drosophila Thor participates in host immune defense and connects a translational regulator with innate immunity [J].
Bernal, A ;
Kimbrell, DA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (11) :6019-6024
[10]   The mTOR inhibitor RAD001 sensitizes tumor cells to DNA-damaged induced apoptosis through inhibition of p21 translation [J].
Beuvink, I ;
Boulay, A ;
Fumagalli, S ;
Zilbermann, F ;
Ruetz, S ;
O'Reilly, T ;
Natt, F ;
Hall, J ;
Lane, HA ;
Thomas, G .
CELL, 2005, 120 (06) :747-759