DLC-1: a Rho GTPase-activating protein and tumour suppressor

被引:163
作者
Durkin, Marian E.
Yuan, Bao-Zhu
Zhou, Xiaoling
Zimonjic, Drazen B.
Lowy, Douglas R.
Thorgeirsson, Snorri S.
Popescu, Nicholas C.
机构
[1] NCI, Ctr Canc Res, Expt Carcinogenesis Lab, Bethesda, MD 20892 USA
[2] NIOSH, Ctr Dis Control, Lab Mol Genet Toxicol, Morgantown, WV USA
[3] NIOSH, Ctr Dis Control, Mol Biol Branch, Morgantown, WV USA
[4] NCI, Canc Res Ctr, Cellular Oncol Lab, Bethesda, MD 20892 USA
关键词
deleted in liver cancer; GTPase activating protein; tumour suppressor; metastasis suppressor; cytoskeletal organization; tensin; focal adhesion; cancer detection; cancer therapy;
D O I
10.1111/j.1582-4934.2007.00098.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The deleted in liver cancer 1 (DLC-1) gene encodes a GTPase activating protein that acts as a negative regulator of the Rho family of small GTPases. Rho proteins transduce signals that influence cell morphology and physiology, and their aberrant up-regulation is a key factor in the neoplastic process, including metastasis. Since its discovery, compelling evidence has accumulated that demonstrates a role for DLC-1 as a bona fide tumour suppressor gene in different types of human cancer. Loss of DLC-1 expression mediated by genetic and epigenetic mechanisms has been associated with the development of many human cancers, and restoration of DLC-1 expression inhibited the growth of tumour cells in vivo and in vitro. Two closely related genes, DLC-2 and DLC-3, may also be tumour suppressors. This review presents the current status of progress in understanding the biological functions of DLC-1 and its relatives and their roles in neoplasia.
引用
收藏
页码:1185 / 1207
页数:23
相关论文
共 133 条
[1]   Give lipids a START: The StAR-related lipid transfer (START) domain in mammals [J].
Alpy, F ;
Tomasetto, C .
JOURNAL OF CELL SCIENCE, 2005, 118 (13) :2791-2801
[2]  
Asada K, 2006, ONCOL REP, V15, P1241
[3]   Gene expression profiling of hairy cell leukemia reveals a phenotype related to memory B cells with altered expression of chemokine and adhesion receptors [J].
Basso, K ;
Liso, A ;
Tiacci, E ;
Benedetti, R ;
Pulsoni, A ;
Foa, R ;
Di Raimondo, F ;
Ambrosetti, A ;
Califano, A ;
Klein, U ;
Favera, RD ;
Falini, B .
JOURNAL OF EXPERIMENTAL MEDICINE, 2004, 199 (01) :59-68
[4]   GAP control: regulating the regulators of small GTPases [J].
Bernards, A ;
Settleman, J .
TRENDS IN CELL BIOLOGY, 2004, 14 (07) :377-385
[5]   GAPs galore! A survey of putative Ras superfamily GTPase activating proteins in man and Drosophila [J].
Bernards, A .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 2003, 1603 (02) :47-82
[6]   Regulating axon branch stability: The role of p190 RhoGAP in repressing a retraction signaling pathway [J].
Billuart, P ;
Winter, CG ;
Maresh, A ;
Zhao, XS ;
Luo, LQ .
CELL, 2001, 107 (02) :195-207
[7]   GEFs and GAPs: Critical elements in the control of small G proteins [J].
Bos, Johannes L. ;
Rehmann, Holger ;
Wittinghofer, Alfred .
CELL, 2007, 129 (05) :865-877
[8]   Evolution of the Rho family of Ras-like GTPases in eukaryotes [J].
Boureux, Anthony ;
Vignal, Emmanuel ;
Faure, Sandrine ;
Fort, Philippe .
MOLECULAR BIOLOGY AND EVOLUTION, 2007, 24 (01) :203-216
[9]   Genome-wide mapping of Polycomb target genes unravels their roles in cell fate transitions [J].
Bracken, AP ;
Dietrich, N ;
Pasini, D ;
Hansen, KH ;
Helin, K .
GENES & DEVELOPMENT, 2006, 20 (09) :1123-1136
[10]   Peroxisome proliferator-activated receptor-γ (PPARγ) inhibits tumorigenesis by reversing the undifferentiated phenotype of metastatic non-small-cell lung cancer cells (NSCLC) [J].
Bren-Mattison, Y ;
Van Putten, V ;
Chan, D ;
Winn, R ;
Geraci, MW ;
Nemenoff, RA .
ONCOGENE, 2005, 24 (08) :1412-1422