博莱霉素和1-硝基芘诱导A/J小鼠肝细胞癌K-ras基因突变模式密码子64

Feng Bai, Yoichi Nakanishi, Koichi Takayama, Xin-Hai Pei, Koji Inoue, Taishi Harada, Miiru Izumi, Nobuyuki Hara
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引用次数: 20

摘要

博莱霉素是一种具有独特基因毒性的模拟放射抗肿瘤药物。1-硝基芘是一种环境诱变剂和致癌物,经历氧化和还原性代谢。在本研究中,雄性A/J小鼠通过腹腔注射博来霉素(120 mg/kg),然后腹腔注射1-硝基芘(总剂量:1575 mg/kg)诱导肝细胞癌。为了了解这两种化合物诱导肝细胞癌的机制,我们分析了这两种肝细胞癌中K-ras原癌基因的突变发生率和谱。应用聚合酶链反应和测序分析方法,对博来霉素和1-硝基芘诱导的肝细胞癌进行K-ras基因外显子1和2点突变的评价。K-ras基因密码子12、13和61的热点区域未发现突变。然而,10例(100%)肝细胞癌中有10例发现K-ras基因的密码子64突变。所有突变均表现出相同的模式,即TAC-CAC过渡。因此,在1-硝基芘存在的情况下,K-ras基因密码子64突变可能在博莱霉素诱导肝细胞癌中起重要作用。据我们所知,这是化学诱导肿瘤中K-ras基因密码子64突变的首次报道。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Codon 64 of K-ras gene mutation pattern in hepatocellular carcinomas induced by bleomycin and 1-nitropyrene in A/J mice.

Bleomycin is a radiomimetic antitumor agent with unique genotoxic properties. 1-nitropyrene is an environmental mutagen and carcinogen that undergoes both oxidative and reductive metabolism. In the present study, hepatocellular carcinomas were induced in male A/J mice by the intraperitoneal injection of bleomycin (120 mg/kg) followed by the intraperitoneal administration of 1-nitropyrene (total dose: 1,575 mg/kg). In order to understand the mechanism by which these two compounds induce hepatocellular carcinomas, the incidence and spectrum of mutations in the K-ras proto-oncogene in these hepatocellular carcinomas were analyzed. The hepatocellular carcinomas were induced by the administration of bleomycin and 1-nitropyrene were evaluated for point mutations in exon 1 and exon 2 of the K-ras gene by the polymerase chain reaction and a sequencing analysis. No mutation was found in the hotspots regions of the K-ras gene codon 12, 13, or 61. However, the codon 64 of the K-ras gene mutation was identified in 10 of 10 (100%) hepatocellular carcinomas. All mutations showed the same pattern, which was TAC-CAC transition. Codon 64 of the K-ras gene mutation may thus play an important role in the induction of hepatocellular carcinomas by bleomycin in the existence of 1-nitropyrene. As far as we know, this is the first report of a codon 64 mutation in the K-ras gene in a chemically induced tumor.

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