Tamura G, Kihana T, Nomura K, Terada M, Sugimura T, Hirohashi S
Division of Pathology, National Cancer Center Research Institute and Hospital, Tokyo, Japan.
Cancer Res. 1991 Jun 1;51(11):3056-8.
Mutations of the p53 gene were investigated after tumor cell enrichment by cell sorting based on differences in DNA content and polymerase chain reaction single-strand conformation polymorphism analysis in 24 surgical specimens of primary gastric cancer. p53 mutations were detected in exons 4-8 in 64% (9 of 14) of aneuploid tumors but in none of 10 diploid tumors examined. Four of five tumors containing two or three aneuploid subpopulations showed the presence of p53 gene mutations. No correlation was found between the presence of p53 mutations and the degree of histological differentiation of tumors. These findings suggest that p53 gene mutations are related to DNA ploidy alterations as relatively late events of carcinogenesis in gastric cancer. The present method is highly sensitive for detection of genetic abnormalities and is applicable even when various kinds of nontumorous cells are present in tumor samples.
在24例原发性胃癌手术标本中,通过基于DNA含量差异的细胞分选富集肿瘤细胞后,研究p53基因的突变情况,并采用聚合酶链反应单链构象多态性分析。在非整倍体肿瘤的64%(14例中的9例)中检测到外显子4 - 8的p53突变,但在检测的10例二倍体肿瘤中均未检测到。含有两个或三个非整倍体亚群的五例肿瘤中有四例显示存在p53基因突变。未发现p53突变的存在与肿瘤的组织学分化程度之间存在相关性。这些发现表明,p53基因突变与DNA倍体改变有关,是胃癌发生过程中相对较晚的事件。本方法对检测基因异常高度敏感,即使肿瘤样本中存在各种非肿瘤细胞也适用。