摘要
背景与目的:研究甲基丙烯酸环氧丙酯(glycidyl methacrylate,GMA)致人支气管上皮(16HBE)恶性转化细胞DNA修复基因点突变情况。材料与方法:采用聚合酶链式反应-限制性片段长度多态性方法(PCR-RFLP)检测GMA致16HBE恶性转化细胞DNA修复基因hMSH2、XRCC1、XPD及XRCC3的重要位点的突变情况,并以DNA测序方法加以验证。结果:16HBE细胞hMSH2IVS12-6(T>C)位点发生了突变,由野生基因型TT型突变为TC基因型,其它位点未检测到突变。DNA测序结果相符。结论:错配修复基因hMSH2IVS12-6(T>C)位点的突变可能为GMA诱导人支气管上皮细胞恶性转化过程中的重要起始分子事件之一。
BACKGROUND AND AIM: To examine the mutation of DNA repair genes of human bronchial epithelial cells malignant transformation induced by glycidyl methacrylate. MATERIALS AND METHODS: To evaluate the mutation of DNA repair genes XRCC1, hMSH2, XPD and XRCC3 by polymerase chain reaction-restriction fragments length polymorphism(PCR-RFLP), and the result was verified by the DNA sequencing. RESULTS: The mutation of hMSH2 IVS12-6 (T〉 C) was observed, while mutations in the other genes were not found.The results from PCR-RFLP and DNA sequencing were consistent. CONCLUSION:The mutation of DNA repair genes hMSH2 WS12-6 (T〉 C)might be important and an initation step during the malignant transformation of human bronchial epithelial cells induced by glycidyl methacrylate.
出处
《癌变.畸变.突变》
CAS
CSCD
2009年第1期1-5,共5页
Carcinogenesis,Teratogenesis & Mutagenesis
基金
国家自然基金资助项目(30671789)