Rho GTPases:: Signaling, migration, and invasion

被引:485
作者
Schmitz, AAP [1 ]
Govek, EE [1 ]
Böttner, B [1 ]
Van Aelst, L [1 ]
机构
[1] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA
基金
美国国家卫生研究院;
关键词
Rho GTPases; signaling; motility; actin cytoskeleton; invasion;
D O I
10.1006/excr.2000.5049
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The acquisition of a motile and invasive phenotype is an important step in the development of tumors and ultimately metastasis. This step requires the abrogation of cell-cell contacts, the remodeling of the extracellular matrix and of cell-matrix interactions, and finally the movement of the cell mediated by the actin cytoskeleton. Evidence for participation of Rho GTPases in migration and invasion is addressed in this review with emphasis on epithelial cells and the contribution of Rho GTPases toward tumor invasion. The Rho GTPases, including Rac, Cdc42, and Rho, have been implicated in the establishment of cell-cell contacts and of cell-matrix interactions crucial to attaining a fully polarized epithelial state, and they are known for their regulation of the actin cytoskeleton and transcriptional activation. Under aberrant conditions, however, they have been implicated in motility, invasion, and some aspects of metastasis. It is well known that Rho GTPases are activated by different classes of transmembrane receptors and that they transmit these signals to their effector proteins. These downstream targets include not only adaptor proteins and kinases which affect the actin cytoskeleton, but also transcription factors leading to expression of genes necessary for the drastic morphological changes which accompany these processes. (C) 2000 Academic Press.
引用
收藏
页码:1 / 12
页数:12
相关论文
共 117 条
[1]   Regulation of microfilament reorganization and invasiveness of breast cancer cells by kinase dead p21-activated kinase-1 [J].
Adam, L ;
Vadlamudi, R ;
Mandal, M ;
Chernoff, J ;
Kumar, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (16) :12041-12050
[2]   Phosphorylation and activation of myosin by Rho-associated kinase (Rho-kinase) [J].
Amano, M ;
Ito, M ;
Kimura, K ;
Fukata, Y ;
Chihara, K ;
Nakano, T ;
Matsuura, Y ;
Kaibuchi, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (34) :20246-20249
[3]   Platelet-derived growth factor and fibronectin-stimulated migration are differentially regulated by the Rac and extracellular signal-regulated kinase pathways [J].
Anand-Apte, B ;
Zetter, BR ;
Viswanathan, A ;
Qiu, RG ;
Chen, J ;
Ruggieri, R ;
Symons, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (49) :30688-30692
[4]  
Aplin AE, 1998, PHARMACOL REV, V50, P197
[5]   Regulation of actin dynamics through phosphorylation of cofilin by LIM-kinase [J].
Arber, S ;
Barbayannis, FA ;
Hanser, H ;
Schneider, C ;
Stanyon, CA ;
Bernard, O ;
Caroni, P .
NATURE, 1998, 393 (6687) :805-809
[6]   Two GTPases, cdc42 and rac, bind directly to a protein implicated in the immunodeficiency disorder Wiskott-Aldrich syndrome [J].
Aspenstrom, P ;
Lindberg, U ;
Hall, A .
CURRENT BIOLOGY, 1996, 6 (01) :70-75
[7]   A novel regulator of p21-activated kinases [J].
Bagrodia, S ;
Taylor, SJ ;
Jordon, KA ;
Van Aelst, L ;
Cerione, RA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (37) :23633-23636
[8]   Motility and invasion are differentially modulated by Rho family GTPases [J].
Banyard, J ;
Anand-Apte, B ;
Symons, M ;
Zetter, BR .
ONCOGENE, 2000, 19 (04) :580-591
[9]  
Birchmeier W, 1995, EXS, V74, P1
[10]   Rho GTPases and their effector proteins [J].
Bishop, AL ;
Hall, A .
BIOCHEMICAL JOURNAL, 2000, 348 (02) :241-255