Frequent epigenetic silencing of PCDH10 by methylation in human colorectal cancer

被引:42
作者
Zhong, Xian [1 ,2 ]
Zhu, Yongliang [3 ]
Mao, Jianshan [3 ]
Zhang, Jiawei [1 ]
Zheng, Shu [1 ]
机构
[1] Zhejiang Univ, Sch Med, Affiliated Hosp 2, Canc Inst,Key Lab Canc Intervent & Prevent,China, Hangzhou 310003, Zhejiang, Peoples R China
[2] Hangzhou Binjiang Hosp, Hangzhou, Zhejiang, Peoples R China
[3] Zhejiang Univ, Sch Med, Affiliated Hosp 2, Dept Gastroenterol, Hangzhou 310003, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
DNA methylation; PCDH10; Tumor suppress gene; Colorectal cancer; DNA METHYLATION; DRINKING-WATER; E-CADHERIN; HYPERMETHYLATION; MICROCYSTIN; SUPPRESSOR; MULTIPLE; ADENOMA; ASSAY; PCR;
D O I
10.1007/s00432-012-1353-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aberrant DNA methylation is common in cancer cells. Epigenetic alterations resulting in the loss of tumor suppression gene functions are frequently involved in tumor development and progression. Recently, methylation of PCDH10 was reported to be associated with multiple hematologic malignancies as well as some solid tumors. Whether the down-regulation of PCDH10 happens in CRC remains unknown. Methylation status of PCDH10 was evaluated by methylation-specific PCR analysis. The effects of PCDH10 re-expression were determined in growth, colony formation, cell cycle, and invasion assays. In this study, we found that 100 % (8 of 8) of colorectal cancer cell lines were silenced for PCDH10, but not normal colorectal epithelial cells. Demethylation treatment confirmed that the reduced expression is associated closely with promoter methylation. Hyper-methylation of PCDH10 was also detected in 85 % of primary colorectal tumors, but not in adjacent normal colorectal tissues. Our results suggest that PCDH10 is an important tumor suppression gene with key roles of suppressing cell proliferation, clonogenicity, and inhibiting cell invasion in the development of colorectal cancer. Thus, PCDH10 methylation may constitute a useful biomarker of colorectal cancer patients.
引用
收藏
页码:485 / 490
页数:6
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