Promoter methylation of TSLC1 and tumor suppression by its gene product in human prostate cancer

被引:91
作者
Fukuhara, H
Kuramochi, M
Fukami, T
Kasahara, K
Furuhata, N
Nobukuni, T
Maruyama, T
Isogai, K
Sekiya, T
Shuin, T
Kitamura, T
Reeves, RH
Murakami, Y
机构
[1] Natl Canc Ctr, Res Inst, Tumor Suppress & Funct Genomics Project, Chuo Ku, Tokyo 1040045, Japan
[2] Kochi Univ, Sch Med, Dept Pathol 2, Nankoku 1738505, Japan
[3] Univ Tokyo, Sch Med, Dept Urol, Bunkyo Ku, Tokyo 1130033, Japan
[4] Johns Hopkins Univ, Sch Med, Dept Physiol, Baltimore, MD 21205 USA
[5] Kochi Univ, Sch Med, Dept Urol, Nankoku 1738505, Japan
来源
JAPANESE JOURNAL OF CANCER RESEARCH | 2002年 / 93卷 / 06期
关键词
prostate cancer; tumor suppressor gene; TSLC1; promoter methylation; suppression of tumorigenicity;
D O I
10.1111/j.1349-7006.2002.tb01297.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We recently identified TSLC1, a tumor suppressor gene in human lung cancer. Gene silencing by promoter methylation has been observed frequently in adenocarcinoma of the lung, liver, and pancreas. Here, we demonstrate that TSLC1 expression is also absent or markedly reduced in 3 of 4 prostate cancer cell lines. Promoter sequences of TSLC1 were heavily methylated in PPC-1 cells that lacked TSLC1 expression, supporting the idea that promoter methylation is strongly correlated with complete loss of gene expression. Promoter sequences of TSLC1 were also methylated significantly in 7 of 22 (32%) primary prostate cancers. Hypermethylation of the promoter occurred not only in advanced tumors, but also in relatively early-stage tumors. Restoration of TSLC1 expression substantially suppressed tumor formation of PPC-1 cells in nude mice. These findings indicate that alteration of TSLC1 is involved in prostate cancer.
引用
收藏
页码:605 / 609
页数:5
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