Secreted frizzled-related protein-5 is epigenetically downregulated and functions as a tumor suppressor in kidney cancer

被引:45
作者
Kawakami, Kazumori [2 ]
Yamamura, Soichiro [2 ]
Hirata, Hiroshi [2 ]
Ueno, Koji [2 ]
Saini, Sharanjot [2 ]
Majid, Shahana [2 ]
Tanaka, Yuichiro [2 ]
Kawamoto, Ken [3 ]
Enokida, Hideki [3 ]
Nakagawa, Masayuki [3 ]
Dahiya, Rajvir [1 ,2 ]
机构
[1] Vet Affairs Med Ctr, Urol Res Ctr 112F, Dept Urol, San Francisco, CA 94121 USA
[2] Univ Calif San Francisco, San Francisco, CA 94121 USA
[3] Kagoshima Univ, Grad Sch Med & Dent Sci, Dept Urol, Kagoshima 890, Japan
关键词
RCC; sFRP-5; methylation; histone modification; tumor suppressor; RENAL-CELL CARCINOMA; ANTAGONIST FAMILY GENES; BETA-CATENIN; HISTONE MODIFICATIONS; DNA METHYLATION; SFRP GENES; PROMOTER METHYLATION; COLORECTAL-CANCER; SIGNALING PATHWAY; CERVICAL-CANCER;
D O I
10.1002/ijc.25357
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Secreted frizzled-related protein-5 (sFRP-5) has been identified as 1 of the secreted antagonists that bind Wnt protein. However, the functional significance of sFRP-5 in renal cell cancer (RCC) has not been reported. We hypothesized that sFRP-5 may be epigenetically downregulated through DNA methylation and histone modification and function as a tumor suppressor gene in RCC. Using tissue microarray and real-time RT-PCR, we found that sFRP-5 was significantly downregulated in kidney cancer tissues and cell lines, respectively. DNA bisulfite sequencing of the sFRP-5 promoter region in RCC cell lines showed it to be densely methylated, whereas there was few promoter methylation in normal kidney. The sFRP-5 expression was restored and the acetylation of H3 and H4 histones associated with the sFRP-5 promoter region were significantly increased after treatment with demethylation agent (5-Aza-dc) and histone deacetylase inhibitor (TSA). When RCC cells were transfected with the sFRP-5 gene, significant inhibition of anchorage independent colony formation and cell invasion were observed compared to controls. The sFRP-5 transfection also significantly induced apoptosis in RCC cells. In conclusion, this is the first report documenting that the sFRP-5 is downregulated by promoter methylation and histone acetylation and functions as a tumor suppressor gene by inducing apoptosis in RCC cells.
引用
收藏
页码:541 / 550
页数:10
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