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对患有和未患有家族性腺瘤性息肉病(FAP)的患者的结直肠肿瘤中的基因改变进行详细分析。

Detailed analysis of genetic alterations in colorectal tumors from patients with and without familial adenomatous polyposis (FAP).

作者信息

Ichii S, Takeda S, Horii A, Nakatsuru S, Miyoshi Y, Emi M, Fujiwara Y, Koyama K, Furuyama J, Utsunomiya J

机构信息

Department of Biochemistry, Cancer Institute, Tokyo, Japan.

出版信息

Oncogene. 1993 Sep;8(9):2399-405.

PMID:8395678
Abstract

To examine early genetic events during colorectal carcinogenesis, we searched for genetic alterations in 75 adenomas from seven patients with familial polyposis coli (FAP) and in 64 sporadic colorectal tumors (63 carcinomas and one adenoma). We investigated germ-line and somatic mutations in the APC gene, somatic mutations in the K-ras and p53 genes, and loss of heterozygosity (LOH) on chromosome 8p21-22. Thirty-two FAP adenomas carried detectable somatic mutations in the APC gene. The frequency of somatic APC mutations among adenomas was the same regardless of differences in size or histopathological classification. On the other hand, K-ras mutation was very rare in small adenomas where dysplasia was mild or moderate but frequent in large adenomas with severe dysplasia. Mutation of the p53 gene was observed in only two adenomas and LOH on 8p22 was detected in none. These results imply that a second 'hit' in the APC gene, but not necessarily mutation in K-ras or p53, is an important and critical event for formation of a colorectal adenoma.

摘要

为了研究结直肠癌发生过程中的早期遗传事件,我们在7例家族性腺瘤性息肉病(FAP)患者的75个腺瘤以及64个散发性结直肠肿瘤(63个癌和1个腺瘤)中寻找遗传改变。我们研究了APC基因的种系和体细胞突变、K-ras和p53基因的体细胞突变以及8号染色体p21-22区域的杂合性缺失(LOH)。32个FAP腺瘤携带可检测到的APC基因体细胞突变。无论腺瘤大小或组织病理学分类如何,腺瘤中体细胞APC突变的频率相同。另一方面,K-ras突变在发育异常为轻度或中度的小腺瘤中非常罕见,但在发育异常严重的大腺瘤中很常见。仅在2个腺瘤中观察到p53基因突变,未检测到8p22区域的LOH。这些结果表明,APC基因的第二次“打击”而非K-ras或p53基因的突变是结直肠腺瘤形成的重要关键事件。

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