Klingel R, Mittelstaedt P, Dippold W G, Meyer zum Büschenfelde K H
First Department of Internal Medicine, University of Mainz, Federal Republic of Germany.
Gut. 1991 Dec;32(12):1508-13. doi: 10.1136/gut.32.12.1508.
The allele distribution of the Ha-ras gene on chromosome 11p was analysed by the restriction fragment length polymorphism of the enzymes Mspl/Hpall in 238 individuals. The investigation covered 116 patients with colorectal carcinoma and 122 patients with Crohn's disease, representing two patient populations with the same ethnic origin, one with a malignant and the other a benign disease of the same organ system. A total of 17 different alleles were detected belonging to the common, intermediate, and rare classes according to the original nomenclature of Ha-ras alleles. Patients with Crohn's disease showed no difference in the distribution of Ha-ras alleles when compared with expected frequencies. In patients with colorectal carcinoma, the frequency of rare alleles was significantly increased compared with the patients with Crohn's disease (chi 2 = 8.166; Fisher's exact test = 0.005) and with a reference population of 424 cancer free individuals (chi 2 = 49.312; Fisher's exact test = 0.000). Homozygosity was not detected for any rare allele. The occurrence of a rare Ha-ras allele was not linked to the location of the colorectal tumour. These results confirm the hypothesis that unique Ha-ras alleles represent an inherited factor which predisposes the development of colorectal cancer.
通过对238名个体进行Mspl/Hpall酶的限制性片段长度多态性分析,研究了11号染色体短臂上Ha-ras基因的等位基因分布情况。该研究涵盖了116名结直肠癌患者和122名克罗恩病患者,这两组患者来自同一族裔,分别患有同一器官系统的恶性疾病和良性疾病。根据Ha-ras等位基因的原始命名法,共检测到17种不同的等位基因,分属于常见、中等和罕见类别。与预期频率相比,克罗恩病患者的Ha-ras等位基因分布没有差异。在结直肠癌患者中,罕见等位基因的频率与克罗恩病患者相比显著增加(卡方检验=8.166;费舍尔精确检验=0.005),与424名无癌个体的参考人群相比也显著增加(卡方检验=49.312;费舍尔精确检验=0.000)。未检测到任何罕见等位基因的纯合性。罕见Ha-ras等位基因的出现与结直肠肿瘤的位置无关。这些结果证实了一个假设,即独特的Ha-ras等位基因是一种遗传因素,易导致结直肠癌的发生。