Nagata Y, Abe M, Kobayashi K, Yoshida K, Ishibashi T, Naoe T, Nakayama E, Shiku H
Department of Oncology, Nagasaki University School of Medicine, Japan.
Cancer Res. 1990 Feb 1;50(3):480-2.
Point mutations of c-ras genes were analyzed in human gastrointestinal cancers. DNA obtained from the tissues was amplified by polymerase chain reaction and then analyzed by dot blot hybridization assay with oligonucleotide probes to detect mutations at codons 12, 13, and 61 of c-Ki-ras, c-Ha-ras, and c-N-ras. In two of 25 cases of stomach cancer point mutations at codon 13 of c-Ki-ras were found. In colorectal cancer, eight of 30 cases showed mutations: four cases of codon 12 and one case at codon 13 of c-Ki-ras and two cases at codon 61 and one case at codon 13 of c-N-ras. These results may indicate involvement of a wide variety of c-ras gene point mutations, in addition to those at codon 12 of c-Ki-ras, in oncogenesis of human gastrointestinal cancers. In all three mutations of c-Ki-ras at codon 13 which had been seldom found in human cancers, glycine to aspartic acid mutations due to identical G to A transition at the second nucleotide were observed.
对人类胃肠道癌症中的c-ras基因点突变进行了分析。从组织中获取的DNA通过聚合酶链反应进行扩增,然后用寡核苷酸探针通过点杂交分析来检测c-Ki-ras、c-Ha-ras和c-N-ras第12、13和61密码子处的突变。在25例胃癌中有2例发现了c-Ki-ras第13密码子的点突变。在结肠癌中,30例中有8例显示出突变:4例c-Ki-ras第12密码子突变、1例c-Ki-ras第13密码子突变、2例c-N-ras第61密码子突变和1例c-N-ras第13密码子突变。这些结果可能表明,除了c-Ki-ras第12密码子处的突变外,多种c-ras基因点突变也参与了人类胃肠道癌症的肿瘤发生过程。在人类癌症中很少发现的c-Ki-ras第13密码子的所有3个突变中,均观察到由于第二个核苷酸处相同的G到A转换导致的甘氨酸到天冬氨酸的突变。