The many faces of the tumor suppressor gene APC

被引:113
作者
van Es, JH
Giles, RH
Clevers, HC
机构
[1] Univ Utrecht, Med Ctr, Dept Immunol, NL-3508 GA Utrecht, Netherlands
[2] Univ Utrecht, Med Ctr, Ctr Biomed Genet, NL-3508 GA Utrecht, Netherlands
关键词
APC; APC2; adenomatous polyposis coli; tumor suppressor gene; cancer;
D O I
10.1006/excr.2000.5142
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Inactivation of the tumor suppressor adenomatous polyposis coli (APC) protein is a critical early step in the development of familial and sporadic colon cancer. Close examination of the function of APC has shown that it is a multifunctional protein involved in a wide variety of processes, including regulation of cell proliferation, cell migration, cell adhesion, cytoskeletal reorganization, and chromosomal stability. Tantalizing clues to the different functions of APC have been provided by the identification of proteins interacting with several discrete motifs within APC. Each of these putative functions could link APC inactivation with tumorigenesis. Here, we will summarize recent findings regarding the diverse role of APC. We will emphasize the interaction of APC with different binding partners, the role of these complex interactions for normal functioning of the cell, and how disruption of these interactions may play a role in tumor development. The rapid progress made recently shows the many faces of APC, leading to a constant reappreciation of this multitasking tumor suppressor protein. (C) 2001 Academic Press.
引用
收藏
页码:126 / 134
页数:9
相关论文
共 83 条
  • [1] beta-catenin is a target for the ubiquitin-proteasome pathway
    Aberle, H
    Bauer, A
    Stappert, J
    Kispert, A
    Kemler, R
    [J]. EMBO JOURNAL, 1997, 16 (13) : 3797 - 3804
  • [2] Differential recruitment of Dishevelled provides signaling specificity in the planar cell polarity and Wingless signaling pathways
    Axelrod, JD
    Miller, JR
    Shulman, JM
    Moon, RT
    Perrimon, N
    [J]. GENES & DEVELOPMENT, 1998, 12 (16) : 2610 - 2622
  • [3] THE TUMOR-SUPPRESSOR GENE-PRODUCT APC BLOCKS CELL-CYCLE PROGRESSION FROM G(0)/G(1) TO S-PHASE
    BAEG, GH
    MATSUMINE, A
    KURODA, T
    BHATTACHARJEE, RN
    MIYASHIRO, I
    TOYOSHIMA, K
    AKIYAMA, T
    [J]. EMBO JOURNAL, 1995, 14 (22) : 5618 - 5625
  • [4] Barker N, 2000, BIOESSAYS, V22, P961
  • [5] Functional interaction of an axin homolog, conductin, with β-catenin, APC, and GSK3β
    Behrens, J
    Jerchow, BA
    Würtele, M
    Grimm, J
    Asbrand, C
    Wirtz, R
    Kühl, M
    Wedlich, D
    Birchmeier, W
    [J]. SCIENCE, 1998, 280 (5363) : 596 - 599
  • [6] Functional interaction of beta-catenin with the transcription factor LEF-1
    Behrens, J
    vonKries, JP
    Kuhl, M
    Bruhn, L
    Wedlich, D
    Grosschedl, R
    Birchmeier, W
    [J]. NATURE, 1996, 382 (6592) : 638 - 642
  • [7] Dishevelled: at the crossroads of divergent intracellular signaling pathways
    Boutros, M
    Mlodzik, M
    [J]. MECHANISMS OF DEVELOPMENT, 1999, 83 (1-2) : 27 - 37
  • [8] Signaling specificity by frizzled receptors in Drosophila
    Boutros, M
    Mihaly, J
    Bouwmeester, T
    Mlodzik, M
    [J]. SCIENCE, 2000, 288 (5472) : 1825 - 1828
  • [9] Brannon M, 1999, DEVELOPMENT, V126, P3159
  • [10] A common human skin tumour is caused by activating mutations in β-catenin
    Chan, EF
    Gat, U
    McNiff, JM
    Fuchs, E
    [J]. NATURE GENETICS, 1999, 21 (04) : 410 - 413