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李华文, 江明, 张和喜, 王小利, 余毅恺, 徐顺清, 周宜开, 吕斌. 肝肿瘤发生中过氧亚硝酸阴离子标志物作用[J]. 中国公共卫生, 2005, 21(11): 1320-1322. DOI: 10.11847/zgggws2005-21-11-23
引用本文: 李华文, 江明, 张和喜, 王小利, 余毅恺, 徐顺清, 周宜开, 吕斌. 肝肿瘤发生中过氧亚硝酸阴离子标志物作用[J]. 中国公共卫生, 2005, 21(11): 1320-1322. DOI: 10.11847/zgggws2005-21-11-23
LI Huawen, JIANG Ming, ZHANG Hexi, . Effects and biomarkers of peroxynitrite on development of liver tumor[J]. Chinese Journal of Public Health, 2005, 21(11): 1320-1322. DOI: 10.11847/zgggws2005-21-11-23
Citation: LI Huawen, JIANG Ming, ZHANG Hexi, . Effects and biomarkers of peroxynitrite on development of liver tumor[J]. Chinese Journal of Public Health, 2005, 21(11): 1320-1322. DOI: 10.11847/zgggws2005-21-11-23

肝肿瘤发生中过氧亚硝酸阴离子标志物作用

Effects and biomarkers of peroxynitrite on development of liver tumor

  • 摘要:
      目的   比较过氧亚硝酸阴离子(ONOO-)对正常人胚肝细胞株L-02和肝母细胞瘤细胞株HepG2 DNA损伤和细胞毒性差异, 探索ONOO-在肝肿瘤发生中的作用及可能标志物.
      方法   0.01, 0.05, 0.1 mmol/L ONOO-作用细胞后, 检测ONOO-对2株肝细胞的细胞生存率, 超氧化物歧化酶(SOD)、谷胱甘肽(GSH)、过氧化氢酶(CAT)、丙二醛(MDA)含量变化, DNA损伤, 生长抑制DNA损伤基因(GADD)表达的影响差异.
      结果   ONOO-使2种肝细胞的生存率下降、SOD含量降低(P<0.05)和CAT、GSH的显著变化, 显著升高MDA的含量;DNA损伤程度和GADD45、GADD153基因表达水平在2株肝细胞均随着剂量的增加显著升高.2种肝细胞相比, 各浓度组L-02细胞损伤程度大于HepG2细胞, 但只有GADD基因表达水平差异有统计学意义(P<0.05).
      结论   ONOO-对正常肝细胞和肝癌细胞均显示细胞毒性作用, 引起DNA损伤, 诱导GADD表达.GADD基因表达水平在不同肝细胞中差异有统计学意义, 可能是ONOO-细胞损伤效应的标志物.

     

    Abstract:
      Objective   To compare the DNA damages and cytotoxicit effect of perox ynitrite(ONOO-)to human embr yoliver L-02 cells and human hepatic tumor HepG 2 cells.
      Methods   Twoliver cells were exposed to different concentration perox ynitrite(0.01, 0.05, 0.1mmol/L).Survival rate, level of superoxide dismutase(SOD), glutamy lcysteiny lgly cine(GSH), catalase(CAT), Malonyldiadehyde(MDA), DNA damage and the expression level of Growth arrestand DNA damag -einducible genes(GADD)were measured.
      Results   Afterexposed to peroxy nitrite, L-02 and HepG 2 cells survival rate decreased from 87.55%, 90.34% to 19.21%, 21.59% varying concentration ranging 0.01mmol/L to 0.2mmol/L, respectively.0.01mmol/L to 0.2mmol/L, respectively.Perox ynitrite caused GSH, CATlevel significantly change, decreased SOD level and increased MED level in L-02 and HepG2 cells(P<0.05).DNA damage and GADD expression level increased as perox ynitrite concentration increased in both two cell lines(P<0.05).All these damages were more serious in L-02 in every concentration level than thatof HepG2, butonly the expression level of GADD were significant difference between L-02 and HepG2 cells.
      Conclusion   Perox ynitrite had cytotoxicity effectand significant difference was observed in two cells.GADD expression level maybe one of the bio markers of NONN- damage effects.

     

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