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硼替佐米联合5-氮杂胞苷对K562细胞凋亡及SHIP mRNA表达的影响

[Effects of bortezomib combined with 5-azacytidine on the apoptosis of K562 cells and expression of SHIP mRNA].

作者信息

Jia Zhi-Qiang, Wei Yu-Tao, Wei Yu-Lian, Su Wei, Yu Chun-Xia, Tao Jin, Rong Hong-Qi

机构信息

Department of Hemotology,Baoding Municipal First Hospital, Baoding 071000, Hebei Province, China. E-mail:

Department of Hemotology,Baoding Municipal First Hospital, Baoding 071000, Hebei Province, China.

出版信息

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2014 Oct;22(5):1291-4. doi: 10.7534/j.issn.1009-2137.2014.05.020.

Abstract

This study was aimed to investigate the effects of bortezomib combined with 5-azacytidine on the apoptosis of K562 cells and expressiom of SHIP mRNA. The K562 cells were cultured and treated with different concentrations of bortezomib, 5-azacytidine or their combination for 24 hours. Then, the expression of SHIP mRNA was detected by RT-PCR,the cell proliferation was analyzed by using MTT assay and flow cytometry. The results showed that 5-20 nmol/L bortezomib could effectively inhibit the proliferation of K562 and this inhibitory effect gradually enhanced along with the increase of bortezomib concentration, the group of bortezomib combined with 5-azacytidine showed more inhibitory effect on K562 cells than that of bortezomib or 5-azacytidine alone.The bortezomib could promote the apoptosis of K562 cells in a dose-dependent manner,and this apoptotic effect was higher in group of bortezomib combined with 5-azacytidine than that in group of bortezomib or 5-azacytidine alone.Bortezomib could down-regulated the expression of SHIP mRNA in a dose-dependent manner,and this down-requlated effect was higher in group of bortezomib combined with 5-azacytidine than that in group of bortezomib or 5-azacytidine alone.It is concluded that bortezomib and 5-azacytidine can induce apoptosis by inhibiting the expression of SHIP mRNA in K562 cells.The combination of bortezomib with 5-azacytidine displays a synergetic effect.

摘要

本研究旨在探讨硼替佐米联合5-氮杂胞苷对K562细胞凋亡及SHIP mRNA表达的影响。培养K562细胞,并用不同浓度的硼替佐米、5-氮杂胞苷或其组合处理24小时。然后,通过RT-PCR检测SHIP mRNA的表达,使用MTT法和流式细胞术分析细胞增殖。结果显示,5-20 nmol/L硼替佐米可有效抑制K562细胞的增殖,且这种抑制作用随硼替佐米浓度的增加而逐渐增强,硼替佐米联合5-氮杂胞苷组对K562细胞的抑制作用比单独使用硼替佐米或5-氮杂胞苷组更强。硼替佐米可呈剂量依赖性地促进K562细胞凋亡,且硼替佐米联合5-氮杂胞苷组的这种凋亡作用比单独使用硼替佐米或5-氮杂胞苷组更高。硼替佐米可呈剂量依赖性地下调SHIP mRNA的表达,且硼替佐米联合5-氮杂胞苷组的这种下调作用比单独使用硼替佐米或5-氮杂胞苷组更高。结论是,硼替佐米和5-氮杂胞苷可通过抑制K562细胞中SHIP mRNA的表达诱导细胞凋亡。硼替佐米与5-氮杂胞苷联合使用具有协同作用。

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