Kawate S, Takenoshita S, Ohwada S, Mogi A, Fukusato T, Makita F, Kuwano H, Morishita Y
Second Department of Surgery, Gunma University School of Medicine, Gunma 371-8511, Japan.
Int J Oncol. 1999 Jan;14(1):127-31. doi: 10.3892/ijo.14.1.127.
Mutations in the transforming growth factor beta type II receptor (TGFbetaRII), Smad2, and Smad4 genes have been detected in several human cancers. However, there are no reports of mutation analysis of the entire coding regions in these genes in hepatocellular carcinoma, and the roles of these genes in hepatocarcinogenesis remain unknown. We screened 30 hepatocellular carcinomas for mutations of these genes using polymerase chain reaction single-strand conformation polymorphism. We detected no mutations, but did find 3 cases of loss of heterozygosity of chromosome 17p13.1. These results suggest that mutations of the TGFbetaRII, Smad2, and Smad4 genes are rare, and that genetic instability is uncommon in human hepatocellular carcinoma.
在几种人类癌症中已检测到转化生长因子βⅡ型受体(TGFbetaRII)、Smad2和Smad4基因的突变。然而,尚无关于肝细胞癌中这些基因整个编码区突变分析的报道,且这些基因在肝癌发生中的作用仍不清楚。我们使用聚合酶链反应单链构象多态性方法筛查了30例肝细胞癌中这些基因的突变情况。我们未检测到突变,但发现3例17p13.1染色体杂合性缺失。这些结果表明,TGFbetaRII、Smad2和Smad4基因的突变很少见,并且遗传不稳定性在人类肝细胞癌中并不常见。