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机构地区:[1]中国医科大学实验技术中心二部 [2]中国医科大学高等职业技术学院,沈阳110001 [3]营口经济技术开发区中心医院检验科,辽宁营口115007
出 处:《中国医科大学学报》2008年第3期346-348,共3页Journal of China Medical University
摘 要:目的研究阿霉素(ADR)与丁酸钠(NaBu)联用对HeLa细胞增殖和端粒酶活性的影响。方法MTT法检测NaBu、ADR以及两药联用的药效动力学特征;TRAP-银染法检测端粒酶活性;RT-PCR法检测hTERT mRNA表达。结果NaBu、ADR以及两药联用均可抑制HeLa细胞生长,ADR单独作用HeLa细胞48h的IC50为6000nmol/L,与1mmol/L的NaBu联用后降为320nmol/L,两组均呈剂量依赖性。ADR组和NaBu+ADR组的端粒酶活性随ADR浓度增加而降低,呈剂量依赖性,在ADR浓度为100nmol/L时差异有统计学意义(P<0.05);hTERT mRNA表达与端粒酶的变化趋势一致,在ADR浓度为10nmol/L、100nmol/L浓度时差异有统计学意义(P<0.05)。结论NaBu和ADR均可抑制HeLa细胞增殖,联合应用具有协同效应,与抑制端粒酶活性、下调hTERT mRNA表达有关。Objective To investigate the effects of Adriamycin (ADR) conibined with sodium Butyrate (NaBu) on HeLa cell proliferation and telomerase activity. Methods the dynamic cytotoxicity of ADR or / and NaBu was evaluated by MTT assay. The telomerase activity was measured by TRAP and silver staining. The expression of hTERT was assessed by RT-PCR. Results HeLa cell growth was inhibited by ADR or / and NaBu. IC50 of ADR alone was 6 000 nmol/L, and decreased to 320 nmol/L when conibined with NaBu. This inhibition of ADR and NaBu+ADR were dose-dependant. The telomerase activities of Hela cells were reduced after treated 48 hours with ADR alone or with NaBu, which were dose-dependant. The difference of both treatments at the concentration of 100 nmol/L was statistically significant (P 〈 0.05). hTERT mRNA of HeLa cells was reduced in RT-PCR,which was consistent with the telomerase activity. The difference of both treatments at the concentration of 10 nmol/L and 100 nmol/L were stistically significant ( P 〈 0.05 ). Conclusion The application of ADR and NaBu can inhibit the proliferation of HeLa cells, and the combination of those two drugs has synergistic effect, which is related to the inhibi- tion of telomerase activity and the derease of hTERT mRNA transcription.
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