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AZT对白血病细胞株KG-1a细胞增殖和端粒酶活性的影响     被引量:4

Effects of AZT on Leukemia Cell Line KG-1a Proliferation and Telomerase Activity

文献类型:期刊文献

中文题名:AZT对白血病细胞株KG-1a细胞增殖和端粒酶活性的影响

英文题名:Effects of AZT on Leukemia Cell Line KG-1a Proliferation and Telomerase Activity

作者:靳蕊蕊[1];晁荣[1];席亚明[1];陈彻[2];楚惠媛[2];李明[1];张豪[1]

第一作者:靳蕊蕊

机构:[1]兰州大学第一医院血液科,血液学研究所;[2]甘肃中医学院

第一机构:兰州大学第一医院血液科,血液学研究所

年份:2012

卷号:20

期号:2

起止页码:277

中文期刊名:中国实验血液学杂志

外文期刊名:Journal of Experimental Hematology

收录:CSTPCD;;Scopus;北大核心:【北大核心2011】;CSCD:【CSCD_E2011_2012】;PubMed;

基金:2010甘肃省财政厅基本科研业务费专用资金(编号甘政财〔2010〕176号);2011年甘肃省普通中医药科研立项资助课题G2K-2011-69

语种:中文

中文关键词:白血病;KG-1a细胞;AZT;端粒酶

外文关键词:leukemia; KG-1a cell; AZT; telomerase

摘要:本研究探索端粒酶抑制剂3'-叠氮-2',3'-脱氧胸腺核苷(AZT)对人急性髓系白血病细胞株KG-1a细胞增殖和端粒酶活性的影响。用MTT法检测不同浓度AZT分别作用24、48、72 h时KG-1a细胞增殖水平;流式细胞术检测AZT对KG-1a细胞周期及细胞凋亡的影响;TRAP-PCR-ELISA法检测细胞端粒酶活性;RT-PCR法检测细胞端粒逆转录酶(hTERT)mRNA的表达。结果表明,AZT能抑制KG-1a细胞增殖,抑制作用具有时间和浓度依赖性;随AZT浓度的增加,处于S期的细胞数目减少,G2/M期细胞数目增加,且出现凋亡峰;AZT作用后实验组细胞的端粒酶活性降低,hTERT-mRNA表达下降,下调程度与AZT浓度呈正相关。结论:AZT在体外能明显抑制KG-1a细胞增殖,并诱导其凋亡,其机制与降低端粒酶活性、下调hTERT mRNA表达有关。
This study was purposed to investigate the effect of 3′-azido-2′,3′-dideoxythymidine(AZT)on the proliferation and telomerase activity of human acute myeloid leukemia cell line KG-1a.The effect of proliferation was detected by MTT assay after the KG-1a cell were stimulated for 24,48 and 72 h with different concentrations of AZT;telomerase activity was detected with TRAP-PCR-ELISA assay;RT-PCR was used to detect telomerase hTERT mRNA expression.The results showed that the proliferation of KG-1a cells was inhibited in a time and concentration dependent manner after exposure to AZT for 24,48 and 72 h;the KG-1a cells decreased in S phase and increased in G2/M phase with the increasing of the concentration of AZT;telomerase activity and hTERT-mRNA expression in the experimental groups decreased after treated with AZT,which was positilvely correlated with concentration of AZT.It is concluded that AZT inhibits KG-1a cell proliferation and induces apoptosis,which maybe related with its decreasing the telomerase activity and hTERT mRNA expression.

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