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GST-π EXPRESSION IN TRANSFORMED CELLS BY TRANSFECTING OF DNA ISOLATED FROM HUMAN FETAL LUNG TISSUES TREATED WITH CARCINOGENS

机译:通过转化经致癌基因治疗的人胎肺组织中分离的DNA,GST-π在转化细胞中的表达

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摘要

Objective: To investigate the relationship between the GSTs, GST-π expression and initiation of lung carcinogenesis. Methods: The Rat-1 cells were transformed by carcinogens (DEN, MNU and CSC) treated fetal lung DNA for 24 h. Results: The GSTs activities toward 1-chloro-2, 4-dinitro-benzene (CDNB) in transformed cells were significantly higher than in the solvent control cells (P<0.05). GST-π content and GST-π mRNA expression level of transformed cells were also higher than those of control cells which were performed by ELISA and Northern blotting method respectively. The results indicated that the higher GSTS activities of transformed cells were due to the increase of GST-π content and the GST-π mRNA overexpressing may be responsible for the increase of GST-π protein level of the transformed cells. Conclusion: The changes of GSTs and GST-π may be considered as the one of the biomarkers of the initiation of human lung carcinogenesis.
机译:目的:探讨GSTs,GST-π表达与肺癌发生开始之间的关系。方法:用致癌物(DEN,MNU和CSC)处理的鼠肺DNA转化Rat-1细胞24小时。结果:转化细胞中GSTs对1-氯-2、4-二硝基苯(CDNB)的活性明显高于溶剂对照细胞(P <0.05)。转化细胞的GST-π含量和GST-πmRNA表达水平也分别高于通过ELISA和Northern印迹法进行的对照细胞。结果表明,转化细胞较高的GSTS活性归因于GST-π含量的增加,而GST-πmRNA的过表达可能是转化细胞GST-π蛋白水平升高的原因。结论:GSTs和GST-π的变化可能被认为是人类肺癌发生的生物标志之一。

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  • 来源
    《中国癌症研究(英文版)》 |1998年第1期|41-45|共5页
  • 作者单位

    Cancer Institute, Chinese Academy of Medical Sciences, and Peking Union Medical College, Beijing 100021;

    Cancer Institute, Chinese Academy of Medical Sciences, and Peking Union Medical College, Beijing 100021;

    Cancer Institute, Chinese Academy of Medical Sciences, and Peking Union Medical College, Beijing 100021;

    Cancer Institute, Chinese Academy of Medical Sciences, and Peking Union Medical College, Beijing 100021;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 chi
  • 中图分类 肿瘤学;
  • 关键词

    GSTs; GST-π; Lung carcinogenesis; Initiation marker;

    机译:GSTs;GST-π;肺癌变;启动标记;
  • 入库时间 2022-08-19 03:43:17
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