Toyooka Shinichi, Tsukuda Kazunori, Ouchida Mamoru, Tanino Motohiko, Inaki Yasuhiko, Kobayashi Kazuyasu, Yano Masaaki, Soh Junichi, Kobatake Takuya, Shimizu Nobuyoshi, Shimizu Kenji
Department of Cancer and Thoracic Surgery, Graduate School of Medicine and Dentistry, Okayama University, Okayama 700-8558, Japan.
Oncol Rep. 2003 Sep-Oct;10(5):1455-9. doi: 10.3892/or.10.5.1455.
Mutation of the Kirsten ras (K-ras) gene is one of most common alterations in solid tumors including lung and colorectal cancers. We developed new enriched PCR-RFLP assay to detect mutations of K-ras codon 61 at the 1st and 2nd letters and non-enriched PCR-RFLP assay to detect the 3rd letter mutation. One mutant allele among 10(3) wild-type alleles was detected by enriched PCR-RFLP assay, while one mutant in 10 wild-type alleles was detected by non-enriched PCR-RFLP assay for codon 61 3rd letter. We then examined K-ras codon 12, 13 and 61 mutations in lung and colorectal cancers using these assays. K-ras codon 12 mutation was detected in 10 of 109 (9%) lung cancer and 19 of 83 (23%) colorectal cancer cases. K-ras codon 13 mutation was detected in 2 of 83 (2%) colorectal and 0 of 109 NSCLC cases, respectively. There was no K-ras codon 61 mutation in either type of cancer. Our results demonstrate that enriched PCR-RFLP is a sensitive assay to detect K-ras codon 61 mutation, however, it was extremely rare in lung and colorectal cancers, suggesting organ-specific pathways in mutagenesis of the ras gene family.
Kirsten 鼠肉瘤病毒癌基因(K-ras)突变是包括肺癌和结直肠癌在内的实体瘤中最常见的改变之一。我们开发了新的富集聚合酶链反应-限制性片段长度多态性分析方法来检测K-ras密码子61第1和第2位字母的突变,以及非富集聚合酶链反应-限制性片段长度多态性分析方法来检测第3位字母的突变。富集聚合酶链反应-限制性片段长度多态性分析方法能检测到10³个野生型等位基因中的1个突变等位基因,而对于密码子61第3位字母的检测,非富集聚合酶链反应-限制性片段长度多态性分析方法能检测到10个野生型等位基因中的1个突变。然后我们使用这些分析方法检测肺癌和结直肠癌中的K-ras密码子12、13和61的突变。在109例肺癌中有10例(9%)检测到K-ras密码子12突变,在83例结直肠癌中有19例(23%)检测到该突变。在83例结直肠癌中有2例(2%)检测到K-ras密码子13突变,在109例非小细胞肺癌病例中未检测到该突变。两种癌症中均未检测到K-ras密码子61突变。我们的结果表明,富集聚合酶链反应-限制性片段长度多态性分析是检测K-ras密码子61突变的一种灵敏方法,然而,该突变在肺癌和结直肠癌中极其罕见,提示ras基因家族诱变存在器官特异性途径。