THE RAS SIGNAL-TRANSDUCTION PATHWAY

被引:329
作者
KHOSRAVIFAR, R [1 ]
DER, CJ [1 ]
机构
[1] UNIV N CAROLINA,CURRICULUM GENET & MOLEC,CHAPEL HILL,NC 27599
关键词
RAS PROTEINS; TYROSINE KINASES; RHO FAMILY; ACTIN;
D O I
10.1007/BF00690419
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Considerable progress has been made over the past year in elucidating the mechanisms by which extracellular signals are transduced via cell surface receptors to trigger changes in gene expression which determine the growth and differentiated state of a cell. In particular, Ras proteins have been implicated as key intermediates that mediate the signal from upstream tyrosine kinases to a downstream cascade of serine/threonine kinases, which then activate nuclear factors that control gene expression and protein synthesis. How Ras proteins function is regulated in this role as a molecular switch, and how the signal is transmitted between the various components of the pathway, are now being determined. Finally, the Rho family of Ras-related proteins, which regulate the actin cytoskeleton, have also been implicated as mediators of oncogenic Ras transformation. The brisk pace at which the key components of Ras-mediated signal transduction pathways are being identified hold great promise that new targets for therapeutic intervention in cancer may now be identified.
引用
收藏
页码:67 / 89
页数:23
相关论文
共 217 条
  • [121] SOMATIC MUTATIONS IN THE NEUROFIBROMATOSIS-1 GENE IN HUMAN TUMORS
    LI, Y
    BOLLAG, G
    CLARK, R
    STEVENS, J
    CONROY, L
    FULTS, D
    WARD, K
    FRIEDMAN, E
    SAMOWITZ, W
    ROBERTSON, M
    BRADLEY, P
    MCCORMICK, F
    WHITE, R
    CAWTHON, R
    [J]. CELL, 1992, 69 (02) : 275 - 281
  • [122] CHARACTERIZATION OF DOWNSTREAM ELEMENTS IN A RAF-1 PATHWAY
    LIAW, GJ
    STEINGRIMSSON, E
    PIGNONI, F
    COUREY, AJ
    LENGYEL, JA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (03) : 858 - 862
  • [123] THE SH2 AND SH3 DOMAIN CONTAINING PROTEIN GRB2 LINKS RECEPTOR TYROSINE KINASES TO RAS SIGNALING
    LOWENSTEIN, EJ
    DALY, RJ
    BATZER, AG
    LI, W
    MARGOLIS, B
    LAMMERS, R
    ULLRICH, A
    SKOLNIK, EY
    BARSAGI, D
    SCHLESSINGER, J
    [J]. CELL, 1992, 70 (03) : 431 - 442
  • [124] REGULATION OF P21RAS ACTIVITY
    LOWY, DR
    ZHANG, KE
    DECLUE, JE
    WILLUMSEN, BM
    [J]. TRENDS IN GENETICS, 1991, 7 (11-12) : 346 - 351
  • [125] POSTTRANSLATIONAL MODIFICATION OF PROTEINS BY ISOPRENOIDS IN MAMMALIAN-CELLS
    MALTESE, WA
    [J]. FASEB JOURNAL, 1990, 4 (15) : 3319 - 3328
  • [126] MANGUES R, 1992, CANCER BIOL, V3, P229
  • [127] TYROSINE PHOSPHORYLATION OF VAV PROTOONCOGENE PRODUCT CONTAINING SH2 DOMAIN AND TRANSCRIPTION FACTOR MOTIFS
    MARGOLIS, B
    HU, P
    KATZAV, S
    LI, W
    OLIVER, JM
    ULLRICH, A
    WEISS, A
    SCHLESSINGER, J
    [J]. NATURE, 1992, 356 (6364) : 71 - 74
  • [128] CLONING BY FUNCTIONAL COMPLEMENTATION OF A MOUSE CDNA-ENCODING A HOMOLOG OF CDC25, A SACCHAROMYCES-CEREVISIAE RAS ACTIVATOR
    MARTEGANI, E
    VANONI, M
    ZIPPEL, R
    COCCETTI, P
    BRAMBILLA, R
    FERRARI, C
    STURANI, E
    ALBERGHINA, L
    [J]. EMBO JOURNAL, 1992, 11 (06) : 2151 - 2157
  • [129] THE GAP-RELATED DOMAIN OF THE NEUROFIBROMATOSIS TYPE-1 GENE-PRODUCT INTERACTS WITH RAS P21
    MARTIN, GA
    VISKOCHIL, D
    BOLLAG, G
    MCCABE, PC
    CROSIER, WJ
    HAUBRUCK, H
    CONROY, L
    CLARK, R
    OCONNELL, P
    CAWTHON, RM
    INNIS, MA
    MCCORMICK, F
    [J]. CELL, 1990, 63 (04) : 843 - 849
  • [130] GAP DOMAINS RESPONSIBLE FOR RAS P21-DEPENDENT INHIBITION OF MUSCARINIC ATRIAL K+ CHANNEL CURRENTS
    MARTIN, GA
    YATANI, A
    CLARK, R
    CONROY, L
    POLAKIS, P
    BROWN, AM
    MCCORMICK, F
    [J]. SCIENCE, 1992, 255 (5041) : 192 - 194