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Role of Point Mutation of the K‐ras Gene in Tumorigenesis of B6C3F1 Mouse Lung Lesions Induced by Urethane

机译:K-ras基因点突变在尿烷诱导的B6C3F1小鼠肺部肿瘤发生中的作用

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摘要

In order to elucidate the role of point mutation of the K‐ras gene in the tumorigenetic process of lung tumors, an experimental model of lung lesions in mice induced by the administration of urethane was used. A total of 135 B6C3F1 male mice, 6 weeks old, were given urethane in the drinking water at 0, 6, 60, 600 or 1200 ppm, and were then killed after varying periods of time. The lung lesions were histologically characterized as hyperplasia, adenoma and adenocarcinoma. Point mutations in codons 12 and 61 of the K‐ras gene were detected by polymerase chain reaction‐restriction fragment length polymorphism (PCR‐RFLP) and confirmed by using dideoxy sequencing analysis. K‐ras gene mutation was identified in 9 (23.7%) of 38 lesions classified as hyperplasia, 31 (46.3%) of 67 adenomas, and 3 (50%) of 6 adenocarcinomas. The most frequent mutation was an AT‐to‐TA transversion at the second base of codon 61 and this pattern accounted for 65% of the three mutant forms observed. These results suggest that the point mutation of K‐ras gene is involved in all stages of mouse lung tumorigenesis, i.e., activation of this gene can also influence the later stages of lung lesions.
机译:为了阐明K-ras基因的点突变在肺部肿瘤发生过程中的作用,使用了氨基甲酸乙酯诱导的小鼠肺部病变实验模型。共有135只6周大的B6C3F1雄性小鼠在饮用水中分别以0、6、60、600或1200 ppm给予氨基甲酸酯,然后在不同时间段后被杀死。肺损伤的组织学特征为增生,腺瘤和腺癌。通过聚合酶链反应限制片段长度多态性(PCR-RFLP)检测到K-ras基因第12和61位密码子的点突变,并通过双脱氧测序分析进行了确认。在38个被分类为增生的病变中,有9个(23.7%)识别出K-ras基因突变,在67个腺瘤中有31个(46.3%),在6个腺癌中有3个(50%)。最常见的突变是在第61个密码子的第二个碱基处发生了AT-to-TA转换,这种模式占观察到的三种突变形式的65%。这些结果表明,K-ras基因的点突变参与了小鼠肺肿瘤发生的所有阶段,即该基因的激活还可以影响肺部病变的晚期。

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