Prostate Stem Cell Antigen, a Presumable Organ-Dependent Tumor Suppressor Gene, is Down-Regulated in Gallbladder Carcinogenesis

被引:37
作者
Ono, Hiroe [2 ]
Hiraoka, Nobuyoshi [3 ]
Lee, Yeon-Su [4 ]
Woo, Sang Myung [5 ]
Lee, Woo Jin [5 ]
Choi, Il Ju [6 ]
Saito, Akira [7 ]
Yanagihara, Kazuyoshi [8 ]
Kanai, Yae [3 ]
Ohnami, Sumiko
Chiwaki, Fumiko
Sasaki, Hiroki
Sakamoto, Hiromi
Yoshida, Teruhiko [1 ]
Saeki, Norihisa
机构
[1] Natl Canc Ctr, Res Inst, Div Genet, Chuo Ku, Tokyo 1040045, Japan
[2] Tokyo Med & Dent Univ, Biomed Sci PhD Program, Tokyo, Japan
[3] Natl Canc Ctr, Res Inst, Div Mol Pathol, Tokyo 1040045, Japan
[4] Natl Canc Ctr, Div Convergence Technol, Gyeonggi Do, South Korea
[5] Natl Canc Ctr, Ctr Liver Canc, Gyeonggi Do, South Korea
[6] Natl Canc Ctr, Ctr Gastr Canc, Gyeonggi Do, South Korea
[7] StaGen Co, Stat Genet Anal Div, Tokyo, Japan
[8] Yasuda Womens Univ, Fac Pharm, Dept Life Sci, Hiroshima, Japan
关键词
GASTRIC SCIRRHOUS CARCINOMA; CANCER; EXPRESSION; ESTABLISHMENT; LINES; PSCA; METASTASIS; GALLSTONES; BLADDER; MARKER;
D O I
10.1002/gcc.20928
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Gallbladder cancer (GBC) is relatively rare but has a high mortality rate. One candidate molecule which might be involved in GBC development is prostate stem cell antigen (PSCA), a glycosylphosphatidylinositol- anchored cell surface antigen with a tissue- specific pattern of expression in the epithelium of several organs, such as the prostate, stomach, bladder, and gallbladder. It is up- regulated in a number of cancers including prostate, urinary bladder, and pancreatic cancers, while it is down- regulated in esophageal and gastric cancers, suggesting that PSCA has an oncogenic activity in the former but a tumor suppressor activity in the latter. However, the precise function of PSCA and the regulatory mechanism for its expression in normal and cancer cells are yet to be determined. In this study, immunohistochemical analyses with a specific antibody revealed that PSCA is down- regulated in non- neoplastic gallbladder lesions such as cholesterolosis, cholecystolithiasis, and cholecystitis (9/17; 53%), and also in adenocarcinoma (40/44; 91%), a common neoplasm in gallbladder. Analyses of the DNA methylation status in the GBC cell lines by bisulfite- Pyrosequencing and a reporter assay for the PSCA promoter activity suggested that the down- regulation is explained, at least partly, by DNA methylation. Moreover, colony formation assay revealed that PSCA has cell- proliferation inhibition activity in the GBC cell lines, which was also observed in vivo. These lines of in vivo and in vitro evidence suggest that PSCA is acting as a tumor suppressor in GBC development. (C) 2011 Wiley Periodicals, Inc.
引用
收藏
页码:30 / 41
页数:12
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