Cell cycle and cancer: Critical events at the G1 restriction point

被引:73
作者
DelSal, G
Loda, M
Pagano, M
机构
[1] NYU, MED CTR, DEPT PATHOL, NEW YORK, NY 10016 USA
[2] NYU, MED CTR, KAPLAN COMPREHENS CANC CTR, NEW YORK, NY 10016 USA
[3] LAB NAZL CIB, I-34012 TRIESTE, ITALY
[4] HARVARD UNIV, SCH MED, BETH ISRAEL DEACONESS MED CTR, DEPT PATHOL, BOSTON, MA 02215 USA
[5] NYU, DEPT PATHOL, MED CTR, NEW YORK, NY 10016 USA
[6] NYU, KAPLAN COMPREHENS CANC CTR, MED CTR, NEW YORK, NY 10016 USA
来源
CRITICAL REVIEWS IN ONCOGENESIS | 1996年 / 7卷 / 1-2期
关键词
cell cycle; cyclin; cyclin-dependent kinase; Cki; tumor suppressor; cancer; .; ...............;
D O I
10.1615/CritRevOncog.v7.i1-2.80
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
In eukaryotic cells, each phase of the cell division cycle is controlled by the sequential activation of various cyclin-dependent kinases (Cdks). These kinases are known to phosphorylate various substrates whose activity is critical for cell cycle progression. As key regulators of the cell cycle, Cdks must be strictly controlled by both extracellular and intracellular signals for adequate responses to occur. There are several distinct molecular mechanisms for controlling the activity of the different Cdks: regulated synthesis and destruction of the activating subunit (cyclin), regulated synthesis and destruction of the inhibitory subunit (Cki), and posttranslational modification of the kinase subunit by highly specific kinases and phosphatases. During the G1 phase of the cell cycle, cells sense, integrate positive and negative signals, and transmit them to the cell cycle machinery. Because of this pivotal role, a vast majority of oncogenic events selectively target elements controlling the G1. In this review we discuss the elements controlling the G1 phase in relationship to the genesis of cancer.
引用
收藏
页码:127 / 142
页数:16
相关论文
共 156 条
[1]   COMPLEXITY OF THE EARLY GENETIC RESPONSE TO GROWTH-FACTORS IN MOUSE FIBROBLASTS [J].
ALMENDRAL, JM ;
SOMMER, D ;
MACDONALDBRAVO, H ;
BURCKHARDT, J ;
PERERA, J ;
BRAVO, R .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (05) :2140-2148
[2]  
ATAIADA P, 1995, EXP CELL RES, V217, P205
[3]   CYCLIN D1 IS A NUCLEAR-PROTEIN REQUIRED FOR CELL-CYCLE PROGRESSION IN G(1) [J].
BALDIN, V ;
LUKAS, J ;
MARCOTE, MJ ;
PAGANO, M ;
DRAETTA, G .
GENES & DEVELOPMENT, 1993, 7 (05) :812-821
[4]   CYCLIN D1 PROTEIN EXPRESSION AND FUNCTION IN HUMAN BREAST-CANCER [J].
BARTKOVA, J ;
LUKAS, J ;
MULLER, H ;
LUTZHOFT, D ;
STRAUSS, M ;
BARTEK, J .
INTERNATIONAL JOURNAL OF CANCER, 1994, 57 (03) :353-361
[5]  
BATES S, 1994, ONCOGENE, V9, P1633
[6]  
BATES S, 1994, ONCOGENE, V9, P71
[7]  
BERENSON JR, 1990, ONCOGENE, V5, P1343
[8]   CYCLIN D1 TRANSGENE IMPEDES LYMPHOCYTE MATURATION AND COLLABORATES IN LYMPHOMAGENESIS WITH THE MYC GENE [J].
BODRUG, SE ;
WARNER, BJ ;
BATH, ML ;
LINDEMAN, GJ ;
HARRIS, AW ;
ADAMS, JM .
EMBO JOURNAL, 1994, 13 (09) :2124-2130
[9]   MICROFILAMENT REORGANIZATION DURING APOPTOSIS - THE ROLE OF GAS2, A POSSIBLE SUBSTRATE FOR ICE-LIKE PROTEASES [J].
BRANCOLINI, C ;
BENEDETTI, M ;
SCHNEIDER, C .
EMBO JOURNAL, 1995, 14 (21) :5179-5190
[10]  
BUCKLEY MF, 1993, ONCOGENE, V8, P2127