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[天然药物成分CDP对癌细胞系的生长抑制及去甲基化作用]

[Growth inhibition and demethylation by a component of natural drug, CDP, in cancer cell lines].

作者信息

Luan Ju, Qin Yang, Xu Dan, Sun Zhi-Lin, Sun Ze-Fang

机构信息

Department of Biochemistry and Molecular Biology, West China School of Preclinical and Forensic Medicine, Sichuan University, Chengdu 610041, China.

出版信息

Sichuan Da Xue Xue Bao Yi Xue Ban. 2005 Nov;36(6):834-8.

PMID:16334566
Abstract

OBJECTIVE

To investigate the inhibition of tumor cell lines' growth and the demethylation of p16 gene by a component of natural drug, CDP.

METHODS

Human liver cancer cell line Huh-7 and breast cancer cell line T47D were treated with the CDP and DNA methyltransferase inhibitor, 5-azacytidine (5-aza-C). The inhibition of growth was assayed by MTT; the methylation status of p16 gene promoter was analyzed by MSP.

RESULTS

  1. The CpG islands in promoter of p16 gene were identified as completely methylated in Huh-7 and T47D. 2. CDP and 5-aza-C inhibited the proliferation of Huh-7 and T47D cell lines in a dose, time-dependent mode. 3. Methylation-specific bands of CpG islands in p16 gene' promoter were still existed in Huh-7 and T47D, while unmethylation-specific bands appeared in Huh-7 after the cells being treated with 25, 50, 75 and 100 micromol/ L of CDP for 6 days as well as in T47D after the cells being treated with 50, 75 and 100 micromol/L of CDP for 6 days. 4. After the cells being treated with 50 micromol/L of CDP, the methylation-specific bands of CpG island in p16 gene' promoter were still existed in Huh-7 and T47D; unmethylation-specific bands appeared at 12 h and lasted to 144 h in Huh-7 while at 72 h and lasted to 144 h in T47D.

CONCLUSION

CDP has inhibition effect on the cancer cell lines and has the ability to reverse the hypermethylated p16 gene promoter. These results suggest that CDP has great potential in the development of effective anticancer drugs.

摘要

目的

研究天然药物成分CDP对肿瘤细胞系生长的抑制作用以及p16基因的去甲基化作用。

方法

用CDP和DNA甲基转移酶抑制剂5-氮杂胞苷(5-aza-C)处理人肝癌细胞系Huh-7和乳腺癌细胞系T47D。采用MTT法检测细胞生长抑制情况;采用甲基化特异性PCR(MSP)法分析p16基因启动子的甲基化状态。

结果

  1. 发现p16基因启动子中的CpG岛在Huh-7和T47D中完全甲基化。2. CDP和5-aza-C以剂量和时间依赖性方式抑制Huh-7和T47D细胞系的增殖。3. p16基因启动子中CpG岛的甲基化特异性条带在Huh-7和T47D中仍然存在,而在用25、50、75和100 μmol/L的CDP处理细胞6天后,Huh-7中出现了非甲基化特异性条带,在用50、75和100 μmol/L的CDP处理细胞6天后,T47D中也出现了非甲基化特异性条带。4. 在用50 μmol/L的CDP处理细胞后,p16基因启动子中CpG岛的甲基化特异性条带在Huh-7和T47D中仍然存在;在Huh-7中,非甲基化特异性条带在12 h出现并持续到144 h,而在T47D中,非甲基化特异性条带在72 h出现并持续到144 h。

结论

CDP对癌细胞系具有抑制作用,并具有逆转p16基因启动子高甲基化的能力。这些结果表明CDP在开发有效的抗癌药物方面具有巨大潜力。

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