Tamura G
Department of Pathology, Iwate Medical University School of Medicine, Morioka, Japan.
Pathol Int. 1996 Nov;46(11):834-41. doi: 10.1111/j.1440-1827.1996.tb03556.x.
Advances in molecular biology have revealed a consistent set of genetic alterations that may correspond to multistep tumor development. The pathogenesis of adenoma and differentiated adenocarcinoma of the stomach are reviewed from a genetic perspective with reference to the colorectal adenoma-carcinoma sequence. The sequential accumulation of genetic alterations characteristic of the colorectal adenoma-carcinoma sequence does not occur between adenoma and differentiated adenocarcinoma of the stomach, although adenomatous polyposis coll (APC) mutation in adenoma, and p53 mutation and loss of heterozygosity (LOH) of DCC (deleted in colorectal cancer) gene in carcinoma are prevalent genetic alterations. Allelotype, LOH and microsatellite analyses have revealed several chromosomal regions of deletion, as well as genetic instability, that accumulate during the development and progression of differentiated adenocarcinomas. However, these alterations are rarely found in adenomas of the stomach. These findings suggest that the adenoma-carcinoma sequence is relatively rare in gastric carcinogenesis, and that most differentiated adenocarcinomas of the stomach develop through a de novo pathway.
分子生物学的进展揭示了一组可能与肿瘤多步骤发展相对应的一致的基因改变。参照结直肠腺瘤-癌序列,从遗传学角度对胃腺瘤和分化型腺癌的发病机制进行综述。尽管腺瘤中的腺瘤性息肉病(APC)突变以及癌中的p53突变和结直肠癌缺失基因(DCC)的杂合性缺失(LOH)是常见的基因改变,但在胃腺瘤和分化型腺癌之间并未出现结直肠腺瘤-癌序列特有的基因改变的顺序积累。等位基因分型、LOH和微卫星分析揭示了在分化型腺癌的发生和发展过程中积累的几个染色体缺失区域以及基因不稳定情况。然而,这些改变在胃腺瘤中很少见。这些发现表明,腺瘤-癌序列在胃癌发生过程中相对少见,并且大多数胃分化型腺癌是通过一条从头开始的途径发展而来的。