Loss of RhoB expression in human lung cancer progression

被引:148
作者
Mazieres, J
Antonia, T
Daste, G
Muro-Cacho, C
Berchery, D
Tillement, V
Pradines, A
Sebti, S
Favre, G
机构
[1] INSERM, U563, Dept Therapeut Innovat & Mol Oncol, Claudius Regaud Inst, F-31052 Toulouse, France
[2] Univ S Florida, Drug Discovery Program, H Lee Moffitt Canc Ctr & Res Inst, Dept Interdisciplinary Oncol, Tampa, FL USA
[3] Univ S Florida, Drug Discovery Program, H Lee Moffitt Canc Ctr & Res Inst, Dept Biochem & Mol Biol, Tampa, FL USA
[4] Purpan Hosp, Dept Pathol, Toulouse, France
关键词
D O I
10.1158/1078-0432.CCR-03-0149
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: RhoB is a low molecular weight GTPase belonging to the Ras protein superfamily. Whereas most Rho proteins have been shown to have a positive role in proliferation and malignant transformation, the specific role of RhoB appears more divergent. We reported previously that RhoB inhibits cell proliferation in various human cancer cells. Here, we studied the specific role played by RhoB in human lung cancer. Experimental Design: We analyzed the expression of RhoB protein by immunostaining in human lung tissues ranging from normal to invasive carcinoma from different histological types in two large independent studies of, respectively, 94 and 45 samples. We then studied the cellular effect of RhoB overexpression in a model of lung cancer (A549, adenocarcinoma) and tumorigenicity in nude mice. Results: We showed in both studies that RhoB protein was expressed in normal lung and decreased dramatically through lung cancer progression (P < 0.01). Interestingly, RhoB expression was lost in 96% of invasive tumors and reduced by 86% in poorly differentiated tumors compared with the nonneoplastic epithelium. Moreover, the loss of expression of RhoB correlated significantly with tumor stage and proliferative index, whereas no correlation was found between RhoB and p53 or Bcl-2 expression. We then showed that ectopic expression of RhoB in lung cancer cell line A549 suppressed cell proliferation, anchorage-independent growth, and xenograft tumor growth in nude mice. Conclusions: RhoB loss of expression occurs very frequently in lung carcinogenesis, reinforcing its putative tumor suppressive activity, and raising the value of its potential use in cancer therapy.
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收藏
页码:2742 / 2750
页数:9
相关论文
共 46 条
[1]  
Adnane J, 2002, CLIN CANCER RES, V8, P2225
[2]  
[Anonymous], 1999, WHO INT HISTOLOGICAL
[3]   RhoB prenylation is driven by the three carboxyl-terminal amino acids of the protein:: Evidenced in vivo by an anti-farnesyl cysteine antibody [J].
Baron, R ;
Fourcade, E ;
Lajoie-Mazenc, I ;
Allal, C ;
Couderc, B ;
Barbaras, R ;
Favre, G ;
Faye, JC ;
Pradines, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (21) :11626-11631
[4]   Rho GTPases and their effector proteins [J].
Bishop, AL ;
Hall, A .
BIOCHEMICAL JOURNAL, 2000, 348 (02) :241-255
[5]   INVASIVE AND METASTATIC POTENTIAL OF A V-HA-RAS-TRANSFORMED HUMAN BRONCHIAL EPITHELIAL-CELL LINE [J].
BONFIL, RD ;
REDDEL, RR ;
URA, H ;
REICH, R ;
FRIDMAN, R ;
HARRIS, CC ;
KLEINSZANTO, AJP .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1989, 81 (08) :587-594
[6]   THE GTPASE SUPERFAMILY - A CONSERVED SWITCH FOR DIVERSE CELL FUNCTIONS [J].
BOURNE, HR ;
SANDERS, DA ;
MCCORMICK, F .
NATURE, 1990, 348 (6297) :125-132
[7]   Both farnesylated and geranylgeranylated RhoB inhibit malignant transformation and suppress human tumor growth in nude mice [J].
Chen, Z ;
Sun, JZ ;
Pradines, A ;
Favre, G ;
Adnane, J ;
Sebti, SM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (24) :17974-17978
[8]   Genomic analysis of metastasis reveals an essential role for RhoC [J].
Clark, EA ;
Golub, TR ;
Lander, ES ;
Hynes, RO .
NATURE, 2000, 406 (6795) :532-535
[9]   THE SMALL GTP-BINDING PROTEINS RAC1 AND CDC42 REGULATE THE ACTIVITY OF THE JNK/SAPK SIGNALING PATHWAY [J].
COSO, OA ;
CHIARIELLO, M ;
YU, JC ;
TERAMOTO, H ;
CRESPO, P ;
XU, NG ;
MIKI, T ;
GUTKIND, JS .
CELL, 1995, 81 (07) :1137-1146
[10]   The expression of Rho proteins decreases with human brain tumor progression:: Potential tumor markers [J].
Forget, MA ;
Desrosiers, RR ;
Del Maestro, RF ;
Moumdjian, R ;
Shedid, D ;
Berthelet, F ;
Béliveau, R .
CLINICAL & EXPERIMENTAL METASTASIS, 2002, 19 (01) :9-15