Wu C, Akiyama Y, Imai K, Miyake S, Nagasaki H, Oto M, Okabe S, Iwama T, Mitamura K, Masumitsu H
Department of Hygiene and Oncology, Tokyo Medical and Dental University School of Medicine, Japan.
Oncogene. 1994 Mar;9(3):991-4.
To determine if the MCC, DCC or p53 gene is associated with susceptibility to hereditary non-polyposis colorectal cancer (HNPCC), these genes in normal cells from 12 HNPCC patients were analysed by polymerase chain reaction-single strand conformation polymorphism analysis. No changes which may alter the amino acid sequences of these genes were detected, suggesting that these genes are not associated with the susceptibility to HNPCC. Only one of nine HNPCC cancers showed mutations in the MCC and p53 genes on the same analysis. Loss of heterozygosity in chromosomes 5q, 17p, 18q and 22 was detected in four of the nine cancers, all of them being positive as to metastasis to lymph nodes. Abnormalities of the (CA)n repeat were found in six cancers, including all four without metastasis. These data indicate that tumor suppressor genes in chromosomes 5q, 17p, 18q and 22 are associated with the late stage of colorectal tumorigenesis in HNPCC, whereas the (CA)n repeat abnormalities are an early event of tumorigenesis and more essential to HNPCC.
为确定MCC、DCC或p53基因是否与遗传性非息肉病性结直肠癌(HNPCC)的易感性相关,采用聚合酶链反应-单链构象多态性分析对12例HNPCC患者正常细胞中的这些基因进行了分析。未检测到可能改变这些基因氨基酸序列的变化,提示这些基因与HNPCC的易感性无关。在同一分析中,9例HNPCC癌中只有1例显示MCC和p53基因发生突变。在9例癌中的4例检测到5号染色体长臂、17号染色体短臂、18号染色体长臂和22号染色体杂合性缺失,所有这些病例均有淋巴结转移。在6例癌中发现(CA)n重复序列异常,包括所有4例无转移的病例。这些数据表明,5号染色体长臂、17号染色体短臂、18号染色体长臂和22号染色体上的抑癌基因与HNPCC结直肠癌发生的晚期相关,而(CA)n重复序列异常是肿瘤发生的早期事件,对HNPCC更为重要。