Ando M, Takemura K, Maruyama M, Endo M, Iwama T, Yuasa Y
Department of Hygiene and Oncology, Tokyo Medical, and Dental University School of Medicine, Japan.
Gastroenterology. 1992 Dec;103(6):1725-31. doi: 10.1016/0016-5085(92)91427-6.
Colorectal carcinomas may be induced from adenomas, or they may occur de novo. To clarify the histogenesis of colorectal carcinomas, point mutations in codon 12 of the c-K-ras 2 gene in neoplasias of familial adenomatous polyposis patients were examined. Nineteen colorectal advanced carcinomas, 135 adenomatous polyps, 9 hyperplastic polyps, and 27 normal colonic mucosae were obtained from 48 patients. In 27 normal mucosae and 9 hyperplastic polyps, a mutation in the K-ras gene was not detected. Mutations were detected as follows: 0 of 24 in adenomas with mild atypia, 10 of 77 in adenomas with moderate atypia, and 24 of 34 in adenomas with severe atypia. The incidence of mutations in c-K-ras 2 codon 12 is correlated with the degree of atypia of adenomas. However, only 5 such mutations were detected in 19 advanced carcinomas, indicating that the mutation frequency in advanced carcinomas is much lower than that in adenomas with severe atypia. If a mutation of c-K-ras 2 gene is an important component in the formation of adenocarcinoma, these results did not confirm the successive development from adenomas with severe atypia to advanced carcinomas as the main route for colorectal carcinogenesis in familial adenomatous polyposis patients.
结直肠癌可能由腺瘤诱发,也可能原发。为阐明结直肠癌的组织发生,对家族性腺瘤性息肉病患者肿瘤形成过程中c-K-ras 2基因第12密码子的点突变进行了检测。从48例患者中获取了19例结直肠进展期癌、135例腺瘤性息肉、9例增生性息肉及27例正常结肠黏膜。在27例正常黏膜和9例增生性息肉中未检测到K-ras基因突变。检测到的突变情况如下:轻度异型增生腺瘤24例中有0例突变,中度异型增生腺瘤77例中有10例突变,重度异型增生腺瘤34例中有24例突变。c-K-ras 2基因第12密码子的突变发生率与腺瘤的异型程度相关。然而,在19例进展期癌中仅检测到5例此类突变,这表明进展期癌的突变频率远低于重度异型增生腺瘤。如果c-K-ras 2基因突变是腺癌形成的重要组成部分,那么这些结果并未证实重度异型增生腺瘤向进展期癌的连续发展是家族性腺瘤性息肉病患者结直肠癌发生的主要途径。