Immunohistochemical analysis and mutational analyses of β-catenin, Axin family and APC genes in hepatocellular carcinomas

被引:78
作者
Ishizaki, Y
Ikeda, S
Fujimori, M
Shimizu, Y
Kurihara, T
Itamoto, T
Kikuchi, A
Okajima, M
Asahara, T
机构
[1] Hiroshima Univ, Grad Sch Biomed Sci, Program Biomed Res, Div Frontier Med Sci,Dept Surg,Minami Ku, Hiroshima 7348551, Japan
[2] Hiroshima Univ, Grad Sch Biomed Sci, Program Biomed Res, Dept Biochem,Div Mol Med Sci,Minami Ku, Hiroshima 7348551, Japan
关键词
beta-catenin; Axin; Wnt; adenomatous polyposis coli; hepatocellular carcinoma;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Several lines of evidence show that the development of hepatocellular carcinoma (HCC) requires an accumulation of genetic alterations. However, molecular mechanism in HCC carcinogenesis remains unsolved. A total of 89 HCC samples were analyzed in this study to determine how alterations in the Wnt signaling pathway associate with the carcinogenesis of HCC. beta-catenin immunohistochemistry showed positive nuclear staining in 24 (27.0%) of the 89 HCC samples, indicating the existence of alterations in the Wnt signaling pathway in those 24 HCC samples. Mutations in the beta-catenin, Axin1 and Axin2 genes were detected in 10 (41.7%), 13 (54.2%) and 9 (37.5%) of the 24 beta-catenin-positive samples, respectively, but no mutation was detected in the APC gene. In conclusion, in addition to mutations in the beta-catenin gene, mutations in the Axin1 and Axin2 genes may alter the Writ signaling pathway, resulting in accumulation of beta-catenin.
引用
收藏
页码:1077 / 1083
页数:7
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