Shitara Y, Yokozaki H, Yasui W, Takenoshita S, Nagamachi Y, Tahara E
First Department of Pathology, Hiroshima University School of Medicine, Hiroshima 734-8551, Japan.
Int J Oncol. 1998 May;12(5):1061-5. doi: 10.3892/ijo.12.5.1061.
Mutations of the transforming growth factor-beta type II receptor (TGF-beta RII) gene have been detected in several human cancers. However, mutation analysis of coding sequences of TGF-beta RII in gastric carcinomas has not yet been fully elucidated. We performed PCR-SSCP analysis and direct DNA sequencing of the entire coding region of TGF- RII in 38 human sporadic gastric cancers and 8 gastric cancer cell lines. Mutations of the TGF-beta RII were detected in two tumors and three cell lines. Two tumors had one base deletion in the polyadenine tract in exon 3, the cystein-rich extracellular domain. Three cell lines had a silent mutation in the kinase domain located in exon 4. Polymorphisms were detected in introns 2 and 3. An a/g polymorphism was observed at the seventh base in intron 2 and an a/t polymorphism was observed at the fourth to last base in intron 3. There were no mutations in exons 1, 2, 5, 6 and 7. These results indicate that the polyadenine tract in the TGF-beta RII is a mutational hot spot in human gastric cancer. However, these results also suggest that mutations of the gene are rare events in human sporadic gastric cancer.
在多种人类癌症中已检测到转化生长因子-βⅡ型受体(TGF-βRII)基因的突变。然而,胃癌中TGF-βRII编码序列的突变分析尚未完全阐明。我们对38例人类散发性胃癌和8种胃癌细胞系进行了TGF-βRII整个编码区的PCR-SSCP分析和直接DNA测序。在2例肿瘤和3种细胞系中检测到TGF-βRII的突变。2例肿瘤在第3外显子富含半胱氨酸的细胞外区域的多聚腺苷酸序列中有1个碱基缺失。3种细胞系在位于第4外显子的激酶结构域中有沉默突变。在内含子2和3中检测到多态性。在内含子2的第7个碱基处观察到a/g多态性,在内含子3的倒数第4个碱基处观察到a/t多态性。第1、2、5、6和7外显子未发现突变。这些结果表明,TGF-βRII中的多聚腺苷酸序列是人类胃癌中的一个突变热点。然而,这些结果也提示该基因的突变在人类散发性胃癌中是罕见事件。