Phosphoinositide 3-kinase controls early and late events in mammalian cell division

被引:117
作者
García, Z [1 ]
Kumar, A [1 ]
Marqués, M [1 ]
Cortés, I [1 ]
Carrera, AC [1 ]
机构
[1] CSIC, Dept Immunol & Oncol, Ctr Nacl Biotecnol, E-28049 Madrid, Spain
关键词
cancer; cell cycle; p85 regulatory subunit; phosphatidylinositol; 3-kinase;
D O I
10.1038/sj.emboj.7600967
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Phosphoinositide 3- kinase ( PI3K) plays a crucial role in triggering cell division. To initiate this process, PI3K induces two distinct routes, of which one promotes cell growth and the other regulates cyclin- dependent kinases. Fine- tuned PI3K regulation is also required for later cell cycle phases. Here, we review the multiple points at which PI3K controls cell division and discuss its impact on human cancer.
引用
收藏
页码:655 / 661
页数:7
相关论文
共 65 条
[1]   Phosphoinositide 3-kinase activation regulates cell division time by coordinated control of cell mass and cell cycle progression rate [J].
Alvarez, B ;
Garrido, E ;
Garcia-Sanz, JA ;
Carrera, AC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (29) :26466-26473
[2]   Forkhead transcription factors contribute to execution of the mitotic programme in mammals [J].
Alvarez, B ;
Martinez, C ;
Burgering, BMT ;
Carrera, AC .
NATURE, 2001, 413 (6857) :744-747
[3]   Class IB-phosphatidylinositol 3-kinase (PI3K) deficiency ameliorates IA-PI3K-induced systemic lupus but not T cell invasion [J].
Barber, DF ;
Bartolomé, A ;
Hernandez, C ;
Flores, JM ;
Fernandez-Arias, C ;
Rodríguez-Borlado, L ;
Hirsch, E ;
Wymann, M ;
Balomenos, D ;
Carrera, AC .
JOURNAL OF IMMUNOLOGY, 2006, 176 (01) :589-593
[4]   PI3Kγ inhibition blocks glomerulonephritis and extends lifespan in a mouse model of systemic lupus [J].
Barber, DF ;
Bartolomé, A ;
Hernandez, C ;
Flores, JM ;
Redondo, C ;
Fernandez-Arias, C ;
Camps, M ;
Ruckle, T ;
Schwarz, MK ;
Rodríguez, S ;
Martinez-A, C ;
Balomenos, D ;
Rommel, C ;
Carrera, AC .
NATURE MEDICINE, 2005, 11 (09) :933-935
[5]   Phosphoinositide 3-kinase signaling in the cellular response to oxidative stress [J].
Barthel, A ;
Klotz, LO .
BIOLOGICAL CHEMISTRY, 2005, 386 (03) :207-216
[6]   The phosphoinositide 3-kinase pathway [J].
Cantley, LC .
SCIENCE, 2002, 296 (5573) :1655-1657
[7]   New insights into tumor suppression: PTEN suppresses tumor formation by restraining the phosphoinositide 3-kinase AKT pathway [J].
Cantley, LC ;
Neel, BG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (08) :4240-4245
[8]   TOR signaling in mammals [J].
Carrera, AC .
JOURNAL OF CELL SCIENCE, 2004, 117 (20) :4615-4616
[9]   Requirement for phosphatidylinositol-3 kinase activity during progression through S-phase and entry into mitosis [J].
Dangi, S ;
Cha, H ;
Shapiro, P .
CELLULAR SIGNALLING, 2003, 15 (07) :667-675
[10]   Regulation of the forkhead transcription factor FKHR, but not the PAX3-FKHR fusion protein, by the serine/threonine kinase Akt [J].
del Peso, L ;
González, VM ;
Hernández, R ;
Barr, FG ;
Núñez, G .
ONCOGENE, 1999, 18 (51) :7328-7333