| Literature DB >> 12883723 |
Shinichi Toyooka1, Kazunori Tsukuda, Mamoru Ouchida, Motohiko Tanino, Yasuhiko Inaki, Kazuyasu Kobayashi, Masaaki Yano, Junichi Soh, Takuya Kobatake, Nobuyoshi Shimizu, Kenji Shimizu.
Abstract
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.Entities:
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Year: 2003 PMID: 12883723 DOI: 10.3892/or.10.5.1455
Source DB: PubMed Journal: Oncol Rep ISSN: 1021-335X Impact factor: 3.906