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曹军, 姜丽平, 耿成燕, 姚晓, 仲来福. 姜黄素致人结肠癌HT-29细胞DNA损伤作用[J]. 中国公共卫生, 2009, 25(6): 665-666. DOI: 10.11847/zgggws2009-25-06-12
引用本文: 曹军, 姜丽平, 耿成燕, 姚晓, 仲来福. 姜黄素致人结肠癌HT-29细胞DNA损伤作用[J]. 中国公共卫生, 2009, 25(6): 665-666. DOI: 10.11847/zgggws2009-25-06-12
CAO Jun, JIANG Li-ping, GENG Cheng-yan, . Comparison of curcumin-induced damage of mitochondrial DNA and nuclear DNA by long PCR[J]. Chinese Journal of Public Health, 2009, 25(6): 665-666. DOI: 10.11847/zgggws2009-25-06-12
Citation: CAO Jun, JIANG Li-ping, GENG Cheng-yan, . Comparison of curcumin-induced damage of mitochondrial DNA and nuclear DNA by long PCR[J]. Chinese Journal of Public Health, 2009, 25(6): 665-666. DOI: 10.11847/zgggws2009-25-06-12

姜黄素致人结肠癌HT-29细胞DNA损伤作用

Comparison of curcumin-induced damage of mitochondrial DNA and nuclear DNA by long PCR

  • 摘要: 目的 探讨姜黄素致人结肠癌HT-29细胞线粒体DNA(mtDNA)和核DNA(nDNA)损伤作用。方法 人结肠癌HT-29细胞暴露于不同质量浓度的姜黄素(0.0,2.5,5.0,10.020.0μg/ml)2h后,采用长链PCR方法分别扩增mtDNA和nDNA片段,琼脂糖凝胶电泳检测扩增产物量。结果 mtDNA扩增产物在5.0μg/ml姜黄素作用下明显下降,在5.0,10.020.0μg/ml作用下mtDNA损伤频率分别为(1.23±0.10),(1.97±0.24)和(5.78±0.62)/10kb,与对照组比较,差异均有统计学意义(P<0.01);nDNA扩增产物在20.0μg/ml姜黄素作用下才明显下降,在5.0,10.0,20.0μg/ml作用下nDNA损伤频率分别为(0.27±0.04),(0.61±0.11)和(1.61±0.12)/10kb,与对照组比较,除5.0μg/ml作用组外差异均有统计学意义(P<0.01)。结论 姜黄素对HT-29细胞的mtDNA和nDNA损伤均呈剂量依赖关系,并且对mtDNA的损伤作用明显大于nDNA。

     

    Abstract: Objective To compare the damage effects of crown in on mitochondrialDNA (mtDNA)and nuclea DNA (nDNA)in human colon cancer cell line HT-29.Methods After HT-29 cells were exposed to various concentrations of cureum in (0,2.5,5.0,10.0,20.0μg/ml) for 2h,high molecular weight DNA was isolated and long polymerase chain reaction (LPCR) assay was perfouned to deteun ine the damage of mtDNA and nDNA.Results A 2h exposure of HT-29 cells to cureum in led to a dose-dependent decrease in the amplification of both mtDNA and nDNA.Loss of amplification of the mtDNA occurred at a lower dose of curcum in (5μg/ml) compared with the nDNA(10μg/ml).For mtDNA,DNA lesion frequencies for groups with different concentrations of cureum in (5,10 and 201μ/ml) were 1.23±0.10,1.97±0.24 and 5.78±0.62 lesions/10kb(P<0.01),and that of for nDNA were 0.27±0.04,0.61±0.11 and 1.61±0.12 lesions/10kb,respectively.Conclusion In HT-29 cells,curcum in induces DNA dam age to both m1DNA and nDNA,and the damage to mtDNA is more serious as compared with nDNA.

     

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