Expansion of CpG Methylation in the SFRP2 Promoter Region during Colorectal Tumorigenesis

被引:0
|
作者
Takeda, Masanori [1 ]
Nagasaka, Takeshi [1 ]
Dong-Sheng, Sun [1 ]
Nishie, Hiroyuki [2 ]
Oka, Tetsuhiro [1 ]
Yamada, Eiji [1 ]
Mori, Yoshiko [1 ]
Shigeyasu, Kunitoshi [1 ]
Morikawa, Tatsuya [1 ]
Mizobuchi, Satoshi [2 ]
Fujiwara, Toshiyoshi [1 ]
机构
[1] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Gastroenterol Surg & Surg Oncol, Okayama 7008558, Japan
[2] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Anesthesiol & Resuscitol, Okayama 7008558, Japan
关键词
BRAF/KRAS mutations; promoter methylation; colorectal cancer; ABERRANT METHYLATION; DNA METHYLATION; BETA-CATENIN; COLON-CANCER; HEPATOCELLULAR-CARCINOMA; EXTENSIVE METHYLATION; FECAL DNA; MUTATIONS; BRAF; KRAS;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Secreted frizzled-related protein 2, (SFRP2) is a Wnt inhibitor whose promoter CpGs were recently found to be methylated at high frequency in colorectal cancers (CRCs). We hypothesized that the pattern of SFRP2 methylation may differ throughout the promoter during progressive tumorigenesis. Using combined bisulfite restriction analysis (COBRA), two methylation-sensitive regions (Regions A and B) of the SFRP2 promoter were investigated in 569 specimens of colorectal tissue: 222 CRCs, 103 adenomatous polyps (APs), 208 normal colonic mucosa from CRC patients (N-Cs), and 36 normal colonic mucosa from subjects with no evidence of colorectal neoplasia at colonoscopy (N-Ns). Extensive (including both Regions A and B) and partial (either Region A or B) SFRP2 methylation levels were found in 61.7% and 24.8% of CRCs, 8.7% and 37.9% of APs, 3.9% and 39.9% of N-Cs, and 0% and 30.6% of N-Ns, respectively. Extensive methylation of the SFRP2 promoter was present primarily in CRCs, while partial methylation was common in APs. Whereas APs with the KRAS mutant showed no correlation to any pattern of SFRP2 methylation, extensive methylation of the SFRP2 promoter was significantly associated with KRAS mutant CRCs (p < .0001), suggesting that genetic alteration in the RAS-RAF pathway might precede the spread of CpG methylation through the SFRP2 promoter, which is observed in over 60% of advanced colorectal tumors.
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页码:169 / 177
页数:9
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