Sutter T, Arber N, Moss S F, Findling R I, Neugut A I, Weinstein I B, Holt P R
Columbia-Presbyterian Cancer Center, College of Physicians and Surgeons, Columbia University, New York, New York 10032, USA.
Dig Dis Sci. 1996 Jan;41(1):115-8. doi: 10.1007/BF02208591.
The reasons for the relatively rare occurrence of small bowel adenocarcinomas when compared to the high frequency of colonic adenocarcinomas are unknown. Activating mutations in the K-ras oncogene occur in about 40% of colonic adenocarcinomas, possibly reflecting the consequences of carcinogenic exposure. To study whether the low incidence of small bowel adenocarcinomas might be due to the absence of activation of cellular oncogenes in small bowel adenocarcinomas, we examined the frequency of K-ras mutations in small bowel adenocarcinomas. K-ras mutations were determined using a polymerase chain reaction (PCR)-based method to detect codon 12 mutations by restriction fragment length polymorphism. PCR amplification was successful in six of nine small bowel adenocarcinoma samples, and revealed point mutations of K-ras at codon 12 in five of these six cases. We conclude that the small bowel might be exposed to carcinogens similar to those responsible for colorectal cancer, but may have developed protective mechanisms against cancer formation.
与结肠癌的高发病率相比,小肠腺癌相对少见的原因尚不清楚。K-ras癌基因的激活突变约发生在40%的结肠腺癌中,这可能反映了致癌物质暴露的后果。为了研究小肠腺癌的低发病率是否可能是由于小肠腺癌中细胞癌基因未被激活,我们检测了小肠腺癌中K-ras突变的频率。使用基于聚合酶链反应(PCR)的方法通过限制性片段长度多态性检测密码子12突变来确定K-ras突变。在9个小肠腺癌样本中的6个中,PCR扩增成功,并在这6个病例中的5个中发现了K-ras密码子12的点突变。我们得出结论,小肠可能暴露于与结直肠癌相关的致癌物中,但可能已经形成了针对癌症形成的保护机制。