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吴根容, 雷毅雄, 乔颖飒. 硫化镍转化人细胞翻译启动因子的异常表达[J]. 中国公共卫生, 2004, 20(11): 1283-1285.
引用本文: 吴根容, 雷毅雄, 乔颖飒. 硫化镍转化人细胞翻译启动因子的异常表达[J]. 中国公共卫生, 2004, 20(11): 1283-1285.
WU Gen-rong, LEI Yi-xiong, QIA Ying-sa. Abnormal expression of TIF3 in transformed cells induced by crystalline nickel sulfide[J]. Chinese Journal of Public Health, 2004, 20(11): 1283-1285.
Citation: WU Gen-rong, LEI Yi-xiong, QIA Ying-sa. Abnormal expression of TIF3 in transformed cells induced by crystalline nickel sulfide[J]. Chinese Journal of Public Health, 2004, 20(11): 1283-1285.

硫化镍转化人细胞翻译启动因子的异常表达

Abnormal expression of TIF3 in transformed cells induced by crystalline nickel sulfide

  • 摘要:
      目的   探讨结晶型硫化镍(NiS)在诱发人支气管上皮细胞(16HBE)恶变过程中蛋白质翻译启动因子(TIF3)的异常表达, 以阐明不容性硫化镍的人类分子致癌机制。
      方法   应用逆转录-聚合酶链式反应(RT-PCR)技术, 以及敏感先进的荧光定量PCR方法, 对异常表达的蛋白质翻译启动因子TIF进行检测。
      结果   相对于非转化对照细胞, RT-PCR实验初步显示, 这些镍转化细胞和成瘤细胞的TIF3基因表达水平显著升高, 平均分别是对照细胞的2和4倍, 表明TIF3的异常表达水平与硫化镍诱发人支气管上皮细胞的恶变程度有关。
      结论   不容性结晶型硫化镍在诱发人支气管上皮细胞恶变过程中, 存在明显的蛋白质翻译启动因子TIF3异常表达现象, 其表达水平与细胞的恶变程度密切相关, 可能是结晶型硫化镍诱发人细胞肿瘤的重要分子致癌机制之一。

     

    Abstract:
      Objective   To explore the molecular mechanisms potentially responsible for carcinogensis due to nickel, and to determine whether the translation initiation factor 3 (TIF3) was overex pressed during malignant transformation of human bronchial epithelial cell lines (16HBE) induced by crystalline nickel sulfide (NiS).
      Methods   The abnormal expression of TIF3 mRNA in malignant transformed human bronchial epithelial cells and tumorigenic cells induced by crystalline NiS were detected with both reverse transcription PCR technique and sensitive fluorescent quantitative PCR assay.
      Results   Compared with non-transformed human bronchial epithelial cells, the results of RT-PCR experiments primarily showed that the transformed cells and tumorigenic cells express high levels of TIF3 mRNA, the over expressions of TIF3 mRNA were further observed in these cells, the levels of TIF3 mRNA, expression in the transformed cells and tumorigenic cells were higher 2 times and 4 times respectively as compared with control cells, indicating that expression level of TIF3 gene was related to malignant degree of the cells.
      Conclusion   There was markedly abnormal expression of TIF3 gene during malignant transformation of human bronchial epithelial cell line induced by crystalline NiS, and the TIF3 expression was associated with malignant degree of the cells. That may be the molecular mechanisms potentially responsible for carcinogensis due to nickel.

     

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