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作 者:杨俊保[1] 谢大英[1] 左瑾 许建宁[1] 方福德[1]
机构地区:[1]北京中国预防医学科学院劳动卫生与职业病研究所,中国医学科学院基础医学研究所
出 处:《癌变.畸变.突变》1994年第1期6-10,共5页Carcinogenesis,Teratogenesis & Mutagenesis
基 金:国家自然科学基金
摘 要:本实验采用Northern印迹杂文方法研究了甲基丙烯酸环氧丙酯(GMA)对金仓鼠胚胎(SHE)细胞原癌基因C─myc和重要功能基因谷胱甘肽S─转移酶p(GST─p)表达的影响.结果表明GMA促进了这些基因的表达,其中GST─p基因在作用2h表达即见增高,5h后达到高水平,直至12h仍维持这一高水平;c─myc基因在12h后出现高水平.本文讨论了GMA诱导上述基因表达的改变与细胞转化之间的可能关系.To explore preliminaryly the mechanism of golden Syrian hamster embryo(SHE)cells transformation induced by glycidyl methacrylate(GMA),the transeriptionalactivities of some singificant genes such as protooncogene myc(c─myc)and glutathioneS─transferase─p(GST─p)in the SHE cells treated with GMA were examined by usingNorthern blot hybridization with corelative labelled probes。It was observed that the ex-pression level of GST─p m RNA began to increas at 2 hours,and reached to a high steadylevel from 5 hours to 12 hours after the SHE cells were trcated with GMA. The expressionof protooncogene myc reached a peak at l2 hours after the SHE cells treated with GMA.The elevation of the transcription of the genes showed that the regulation of expression ofthe cell genes might be effected by the interference of GMA. We concluded that the activation of expression of c─myc and GST─p gene is important and an initiation step dur- ing the transformation of SHE cells by GMA was discussed.
分 类 号:R730.231.1[医药卫生—肿瘤]
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