Spandidos D A, Glarakis I S, Kotsinas A, Ergazaki M, Kiaris H
Institute of Biological Research and Biotechnology, National Hellenic Research Foundation, Athens, Greece.
Tumori. 1995 May-Jun;81(3 Suppl):7-11.
Activation of ras family genes has been implicated in colorectal tumourigenesis. K-ras is the most frequently altered gene in colorectal neoplasias. The major activating mechanism involves point mutations, although recent data have shown a more complex role, through qualitative alterations. The incidence of codon 12 mutations in K-ras and N-ras genes in patients with primary colorectal adenocarcinomas was examined. We employed a non radioactive PCR-RFLP assay for the detection of mutant samples. We found a significant K-ras activation at codon 12 (38%), while the incidence of N-ras codon 12 activation was limited to 1.5%. These results are in agreement with previous reports. Association has been investigated with clinical and histopathological parameters. Point mutations appear to be more frequent in carcinomas with elements indicating a development from adenoma, in ages below 50 years, in females who had the tumor located at the rest of the large bowel in comparison with rectosigmoid and in higher grade of differentiation.
ras家族基因的激活与结直肠癌的发生有关。K-ras是结直肠肿瘤中最常发生改变的基因。主要的激活机制涉及点突变,尽管最近的数据显示通过定性改变其作用更为复杂。我们检测了原发性结直肠腺癌患者中K-ras和N-ras基因第12密码子突变的发生率。我们采用非放射性PCR-RFLP分析法检测突变样本。我们发现第12密码子处K-ras有显著激活(38%),而N-ras第12密码子激活的发生率仅为1.5%。这些结果与先前的报道一致。我们还研究了其与临床和组织病理学参数的关联。在具有腺瘤发展迹象的癌、50岁以下、肿瘤位于大肠其余部位而非直肠乙状结肠的女性以及高分化程度的癌中,点突变似乎更为常见。