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茶多酚和茶色素对肝癌细胞株HepG2细胞周期的影响 被引量:7

Effects of tea polyphenols and tea pigments on cell cycle of HepG2 cells
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摘要 为探讨茶对肝癌细胞周期的影响 ,体外培养人肝癌细胞株HepG2 ,加入终浓度为 50mg L和 1 0 0mg L茶多酚和茶色素作用 48h后 ,流式细胞仪分析DNA含量 ,Westernblot观察对细胞周期蛋白P2 1 WAF1 CIP1 和细胞周期素D1 (cyclinD1 ) ,RT PCR检测细胞周期素依赖激酶 4 (Cdk4)在mRNA水平上的表达情况。结果表明 ,茶多酚和茶色素引起了细胞周期G1 期阻滞 (G1 arrest) ,抑制了cyclinD1蛋白的表达 ,诱导了P2 1 WAF1 CIP1 蛋白的表达增加 ,并且显著抑制了Cdk4在mRNA水平上的表达。因此 。 The effects of tea polyphenols and tea pigments on cell cycle of hepatic cancer cells were studied. HepG2 cells were incubated with 50 and 100 mg/L tea polyphenols and tea pigments for 48h respectively. Flow cytometry, Western blot and RT PCR analysis were used. Flow cytometry analysis showed that tea polyphenols and tea pigments induced G 1 arrest. Western blot analysis showed tea polyphenols and tea pigments significantly inhibited the expression of cyclin D1 protein and induced higher expression of P21 WAF1/CIP1 protein. The result of RT PCR analysis demonstrated that Cdk4 was significantly inhibited by tea polyphenols and tea pigments. It is concluded that the induction of cell cycle arrest may be an important mechanism of tea on cancer prevention.
出处 《卫生研究》 CAS CSCD 北大核心 2002年第5期358-360,共3页 Journal of Hygiene Research
基金 国家自然科学基金资助项目(No .39970 6 39)
关键词 茶多酚 茶色素 细胞周期 肿瘤 预防 肝癌 tea polyphenols, tea pigments, cell cycle
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参考文献6

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同被引文献88

  • 1周才琼,周张章,范勇,张鹰,阳长敏.不同茶样冲泡浸出液对NO_2^-清除作用的体外试验研究[J].茶叶科学,2004,24(3):201-206. 被引量:21
  • 2贾旭东,韩驰,陈君石.茶多酚和茶色素对人肝癌细胞株HepG2细胞凋亡的影响[J].卫生研究,2005,34(1):73-75. 被引量:17
  • 3梁远亮.茶叶有害物质会否转移到茶饮料[J].质量与市场,2005(3):45-45. 被引量:4
  • 4古小玲,鲁成银,刘新,于良子,陈利燕,汪庆华.茶叶中亚硝酸盐检测技术研究[J].茶叶科学,2007,27(2):159-162. 被引量:12
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  • 8Kuo PL, Lin CC. Green tea constituent (-)-epigallocatechin-3-gallate inhibits Hep G2 cell proliferation and induces apoptosis through p53- dependent and Fas-mediated pat hways [J]. J Biomed Sci, 2003,10 (2) : 219 - 227.
  • 9Nishikawa T,Nakajima T, Moriguchi M,et al. A green tea polyphenol, epigallocatechin-3-gallate, induces apoptosis of human hepatocellular carcinoma, possibly through inhibition of Bcl-2 family proteins [J]. Journal of Hepatology, 2006,44(6):1074-1082.
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