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PMID: 15102679 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Loss of RhoB expression in human lung cancer progression.

Mazieres J, Antonia T, Daste G, Muro-Cacho C, Berchery D, Tillement V, Pradines A, Sebti S, Favre G

Abstract

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. 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. 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. 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.

MeSH Terms
Animals Blotting, Western Carcinoma/metabolism Cell Adhesion Cell Division Cell Line, Tumor Disease Progression Female Humans Immunohistochemistry Ki-67 Antigen/biosynthesis Lung/metabolism Lung Neoplasms/metabolism,pathology Mice Mice, Nude Proto-Oncogene Proteins c-bcl-2/metabolism Time Factors Transfection rhoB GTP-Binding Protein/biosynthesis
Chemicals
Ki-67 Antigen Proto-Oncogene Proteins c-bcl-2 rhoB GTP-Binding Protein
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Mazieres Julien
Institut National de la Santé et de la Recherche Médicale U563, Department of Therapeutic Innovation and Molecular Oncology. Claudius Regaud Institute, Toulouse, France.
Antonia Teresita
Daste Ghislaine
Muro-Cacho Carlos
Berchery Delphine
Tillement Vanessa
Pradines Anne
Sebti Said
Favre Gilles
Article Info
Journal
Clinical cancer research : an official journal of the American Association for Cancer Research
Abbr.
Clin Cancer Res
ISSN
1078-0432
Published
2004-04-15
Pages
2742-50
Language
English
Region
United States
NLM ID
9502500
Subset
IM
Grants
NCI NIH HHS · CA67771 · United States
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