Losi L, Ponz de Leon M, Jiricny J, Di Gregorio C, Benatti P, Percesepe A, Fante R, Roncucci L, Pedroni M, Benhattar J
University Institute of Pathology, Lausanne, Switzerland.
Int J Cancer. 1997 Feb 20;74(1):94-6. doi: 10.1002/(sici)1097-0215(19970220)74:1<94::aid-ijc16>3.0.co;2-i.
Genetic instability related to defective DNA mismatch repair genes may be involved in the pathogenesis of carcinoma in Hereditary Non-Polyposis Colorectal Cancer (HNPCC). To test that the targets of genetic instability could include critical transforming genes involved in colon tumor progression, we examined 23 colorectal carcinomas in patients with HNPCC in order to detect somatic mutations in K-ras and p53 genes. Using single strand conformation polymorphism followed by direct DNA sequencing, we detected 4 mutations in K-ras gene (17%) and 3 in p53 gene (13%) which change the amino acid sequence of the protein p53. This is significantly lower than in sporadic cancer. Our data suggest that colon cancer in HNPCC might partly involve a distinct pathogenetic mechanism that involves other genes than those altered in sporadic tumors.
与DNA错配修复基因缺陷相关的基因不稳定可能参与遗传性非息肉病性结直肠癌(HNPCC)的癌变过程。为了验证基因不稳定的靶点可能包括参与结肠肿瘤进展的关键转化基因,我们检测了23例HNPCC患者的结直肠癌,以检测K-ras和p53基因的体细胞突变。通过单链构象多态性分析并直接进行DNA测序,我们在K-ras基因中检测到4个突变(17%),在p53基因中检测到3个突变(13%),这些突变改变了p53蛋白的氨基酸序列。这显著低于散发性癌症。我们的数据表明,HNPCC中的结肠癌可能部分涉及一种独特的发病机制,该机制涉及的基因不同于散发性肿瘤中发生改变的基因。