Genetic, epigenetic, and clinicopathologic features of gastric carcinomas with the CpG island methylator phenotype and an association with Epstein-Barr virus

被引:143
作者
Kusano, M
Toyota, M
Suzuki, H
Akino, K
Aoki, F
Fujita, M
Hosokawa, M
Shinomura, Y
Imai, K
Tokino, T
机构
[1] Sapporo Med Univ, Canc Res Inst, Dept Internal Med 1, Chuo Ku, Sapporo, Hokkaido 0608543, Japan
[2] Sapporo Med Univ, Canc Res Inst, Dept Mol Biol, Sapporo, Hokkaido 0608543, Japan
[3] Japan Sci & Technol Agcy, PRESTO, Kawaguchi, Japan
[4] Sapporo Med Univ, Dept Publ Hlth, Sapporo, Hokkaido 0608543, Japan
[5] Sapporo Med Univ, Informat Ctr Comp Commun, Sapporo, Hokkaido 0608543, Japan
[6] Keiyukai Sapporo Hosp, Keiyukai Inst Clin Pathol, Sapporo, Hokkaido, Japan
[7] Keiyukai Sapporo Hosp, Dept Surg, Sapporo, Hokkaido, Japan
关键词
gastric carcinoma; DNA methylation; molecular profiling; clinicopathologic features; Epstein-Barr virus;
D O I
10.1002/cncr.21789
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. The CpG island methylator phenotype (CIMP), which is characterized by simultaneous methylation of the CpG islands of multiple genes, has been recognized as one of the important mechanisms in gastrointestinal carcinogenesis. METHODS. Methylation of the 5 methylated-in-tumors (MINT) loci and 12 tumor-related genes in 78 primary gastric carcinomas was examined using combined-restriction analysis. Epstein-Barr virus (EBV)-associated gastric tumors bisulfite were detected using real-time polymerase chain reaction analysis followed by all evaluation of the correlations between CIMP status, EBV-association, and genetic alteration of p53 and K-ras. The authors compared the clinicopathologic features of gastric carcinomas that had high CIMP methylation (CIMP-H) with tumors that had low CIMP methylation (CIMP-L) or negative CIMP methylation (CIMP-N). RESULTS. The methylation profiles of 12 genes showed non-random methylation, Supporting the presence of CIMP in gastric carcinoma. No p53 mutations were detected among CIMP-H tumors, and no EBV association was detected in tumors that showed mutation of p53 and K-ras. In a multiple logistic regression model with CIMP-H as the dependent variable, proximal location (P =.011), diffuse type (P =.019), and less advanced pathologic TNM status (P =.043) contributed significantly to CIMP-H. Patients who had CIMP-N gastric tumors had a significantly worse Survival than patients who had CIMP-H tumors (P =.004) or CIMP-L tumors (P =.012). EBV-associated tumors were associated strongly with CIMP-H, hypermethylation of tumor-related genes, and no p53 or K-ras mutation. CONCLUSIONS. CIMP status appeared to be associated with distinct genetic, epigenetic, and clinicopathologic features in gastric carcinomas. The finding that gastric carcinomas arose through different molecular pathways may affect not only tumor characteristics but also patient prognosis.
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页码:1467 / 1479
页数:13
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