Sasaki M, Sugio K, Sasazuki T
Department of Genetics, Kyushu University, Fukuoka, Japan.
Cancer. 1990 Jun 1;65(11):2576-9. doi: 10.1002/1097-0142(19900601)65:11<2576::aid-cncr2820651130>3.0.co;2-4.
K-ras gene mutation in colorectal tumors from patients with familial polyposis coli were investigated using oligonucleotide probes specific for a mutation at codon 12, 13, or 61 of the K-ras gene. The authors examined 22 colorectal carcinomas and 51 colorectal adenomas from 41 familial polyposis coli patients and observed mutations at codons 12 and 13 in eight of 22 colorectal carcinomas (36%) and six of 51 colorectal adenomas (12%). Thus, the frequency and sites of K-ras gene mutation in colorectal carcinoma from familial polyposis coli patients are similar to those in cases of sporadic colorectal carcinoma and may not be the first genetic event linked to the tumorigenesis.
使用针对K-ras基因第12、13或61密码子突变的寡核苷酸探针,对家族性腺瘤性息肉病患者的结直肠肿瘤中的K-ras基因突变进行了研究。作者检查了41例家族性腺瘤性息肉病患者的22例结直肠癌和51例结直肠腺瘤,在22例结直肠癌中有8例(36%)、51例结直肠腺瘤中有6例(12%)观察到第12和13密码子的突变。因此,家族性腺瘤性息肉病患者结直肠癌中K-ras基因突变的频率和位点与散发性结直肠癌病例相似,可能不是与肿瘤发生相关的首个遗传事件。