Greco C, Gandolfo G M, Mattei F, Gradilone A, Alvino S, Pastore L I, Casale V, Casole P, Grassi A, Cianciulli A M
Clinical Pathology Department, Regina Elena Institute for Cancer Research, Rome, Italy.
Anticancer Res. 1994 May-Jun;14(3B):1433-40.
C-myb structural alterations were analysed by Southern blot hybridization in 55 adenomatous polyps and 21 adenocarcinomas of the colon. Gene amplification was observed in 8 cases (14.5%) and c-myb rearrangements in 3 cases (5.4%) of the preneoplastic lesions analysed. A higher percentage of c-myb abnormalities (23.8%) was shown by malignant tumors. As far as mutant p53 protein is concerned, it was detected both in sera of adenoma and adenocarcinoma patients, though at different levels. No statistically significant correlations were found between c-myb or p53 abnormalities and clinico-pathological variables.
通过Southern印迹杂交分析了55例结肠腺瘤性息肉和21例结肠癌中的C-myb结构改变。在所分析的癌前病变中,8例(14.5%)观察到基因扩增,3例(5.4%)出现c-myb重排。恶性肿瘤显示出更高比例的c-myb异常(23.8%)。就突变型p53蛋白而言,在腺瘤和腺癌患者的血清中均检测到,不过水平不同。未发现c-myb或p53异常与临床病理变量之间存在统计学显著相关性。