Restoration of DLC-1 gene expression induces apoptosis and inhibits both cell growth and tumorigenicity in human hepatocellular carcinoma cells

被引:125
作者
Zhou, XL [1 ]
Thorgeirsson, SS [1 ]
Popescu, NC [1 ]
机构
[1] NCI, Ctr Canc Res, Expt Carcinogenesis Lab, Bethesda, MD 20892 USA
关键词
DLC-1; function; cell growth inhibition; cell migration inhibition; apoptosis reduction of tumorigenicity;
D O I
10.1038/sj.onc.1207246
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
The gene deleted in liver cancer-1 (DLC-1) is located on human chromosome 8p21-22, a region thought to harbor tumor suppressor genes on the basis of its frequent deletion or loss of heterozygosity in a variety of human cancers, including hepatocellular carcinoma (HCC). Deletion or altered expression of DLC-1 is common in HCC. In the current study, the subcellular localization of Dlc-1 protein was determined by immunostaining with antibody to DLC-1 and the possible tumor growth suppressor activity of DLC-1 was investigated by examining the effects of of DLC-1 cDNA transfection in two human HCC cell lines lacking expression of the endogenous gene. The results show that Dlc-1protein is localized in the cell cytoplasm, and the restoration of DLC-1 expression in HCC cells resulted in caspase-3-mediated apoptosis, inhibition of cell growth and invasiveness in vitro as well as in reduction of the ability of the cells to form tumors in athymic nude mice. These observations thus support the notion that Dlc-1 protein is involved in hepatocarcinogenesis and has oncosuppressive activity in HCC.
引用
收藏
页码:1308 / 1313
页数:6
相关论文
共 28 条
[1]   The role of Rho GTPases in disease development [J].
Boettner, B ;
Van Aelst, L .
GENE, 2002, 286 (02) :155-174
[2]   Deleted in liver cancer (DLC) 2 encodes a RhoGAP protein with growth suppressor function and is underexpressed in hepatocellular carcinoma [J].
Ching, YP ;
Wong, CM ;
Chan, SF ;
Leung, THY ;
Ng, DCH ;
Jin, DY ;
Ng, IOL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (12) :10824-10830
[3]  
Euer N, 2002, ANTICANCER RES, V22, P733
[4]   BCL-2 family members and the mitochondria in apoptosis [J].
Gross, A ;
McDonnell, JM ;
Korsmeyer, SJ .
GENES & DEVELOPMENT, 1999, 13 (15) :1899-1911
[5]   ESTABLISHMENT AND CHARACTERIZATION OF A NEW HUMAN HEPATOCELLULAR-CARCINOMA CELL-LINE [J].
HE, L ;
ISSELBACHER, KJ ;
WANDS, JR ;
GOODMAN, HM ;
SHIH, C ;
QUARONI, A .
IN VITRO-JOURNAL OF THE TISSUE CULTURE ASSOCIATION, 1984, 20 (06) :493-504
[6]   A DUAL FUNCTIONAL SIGNAL MEDIATOR SHOWING RHOGAP AND PHOSPHOLIPASE C-DELTA STIMULATING ACTIVITIES [J].
HOMMA, Y ;
EMORI, Y .
EMBO JOURNAL, 1995, 14 (02) :286-291
[7]   BH3-Only proteins - Essential initiators of apoptotic cell death [J].
Huang, DCS ;
Strasser, A .
CELL, 2000, 103 (06) :839-842
[8]   Rho GTPases in transformation and metastasis [J].
Jaffe, AB ;
Hall, A .
ADVANCES IN CANCER RESEARCH, VOL 84, 2002, 84 :57-80
[9]   Loss of heterozygosity of chromosome 8p and 11p in the dysplastic nodule and hepatocellular carcinoma [J].
Kahng, YS ;
Lee, YS ;
Kim, BK ;
Park, WS ;
Lee, JY ;
Kang, CS .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2003, 18 (04) :430-436
[10]   A multigenic program mediating breast cancer metastasis to bone [J].
Kang, YB ;
Siegel, PM ;
Shu, WP ;
Drobnjak, M ;
Kakonen, SM ;
Cordón-Cardo, C ;
Guise, TA ;
Massagué, J .
CANCER CELL, 2003, 3 (06) :537-549