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靶向信号转导和转录激活因子3的小分子干扰RNA增强阿霉素的抗肿瘤活性

[Small interfering RNA targeting STAT3 enhances antitumor activity of doxorubicin].

作者信息

Wang Tian-Xiao, Wang Ying-Ying, Zhang Zhong-Qing

机构信息

Institute of Chinese Materia Medica, College of Pharmacy, Henan University, Kaifeng 475004, China.

出版信息

Yao Xue Xue Bao. 2013 Jan;48(1):52-8.

Abstract

This study is to investigate the effect of small interfering RNA targeting STAT3 (STAT3-siRNA) enhancing antitumor activity of doxorubicin. RT-PCR and Western blotting were used to test the expression of STAT3 mRNA and protein in the HepG2, HeLa and K562/DOX cells and the effect of STAT3-siRNA on the expression of STAT3 mRNA and protein. MTT and Trypan blue assay were performed to determine the inhibitory effect of STAT3-siRNA on HepG2, HeLa and K562/DOX cells and the effect of STAT3-siRNA enhancing antitumor activity of doxorubicin. The effects of STAT3-siRNA on intracellular accumulation of doxorubicin and cell apoptosis were performed by Arrary Scan V(TI)HCS600 High-Contents. The results showed that STAT3 gene, STAT3 and pSTAT3 protein were highly expressed in HepG2, HeLa and K562/DOX cells and STAT3-siRNA decreased the expression of STAT3 mRNA and protein. STAT3-siRNA inhibited the growth of HepG2, HeLa and K562/DOX cells. STAT3-siRNA in combination with doxorubicin decreased by 3.13, 5.22 and 1.74 fold of IC50 of HepG2, HeLa and K562/DOX cells compared with doxorubicin only. Intracellular accumulation of doxorubicin increased by 16.8%, 12.87% and 25.67% respectively in HepG2, HeLa and K562/DOX cells in the presence of STAT3-siRNA. An enhancement of doxorubicin-induced cell apoptosis was observed in HepG2, HeLa and K562/DOX cells treated with STAT3-siRNA. The results suggested that STAT3-siRNA could enhance the antitumor activity of doxorubicin on HepG2, HeLa and K562/DOX cells.

摘要

本研究旨在探讨靶向信号转导和转录激活因子3(STAT3)的小干扰RNA(STAT3-siRNA)增强阿霉素抗肿瘤活性的作用。采用逆转录聚合酶链反应(RT-PCR)和蛋白质免疫印迹法检测STAT3 mRNA和蛋白在肝癌细胞系HepG2、宫颈癌细胞系HeLa和耐阿霉素的人慢性髓原白血病细胞系K562/DOX中的表达情况以及STAT3-siRNA对其表达的影响。采用噻唑蓝比色法(MTT)和台盼蓝染色法检测STAT3-siRNA对HepG2、HeLa和K562/DOX细胞的抑制作用以及STAT3-siRNA增强阿霉素抗肿瘤活性的作用。通过Array Scan V(TI)HCS600高内涵成像系统检测STAT3-siRNA对阿霉素细胞内蓄积及细胞凋亡的影响。结果显示,STAT3基因、STAT3及磷酸化STAT3蛋白在HepG2、HeLa和K562/DOX细胞中高表达,而STAT3-siRNA可降低STAT3 mRNA和蛋白的表达。STAT3-siRNA可抑制HepG2、HeLa和K562/DOX细胞的生长。与单纯阿霉素相比,STAT3-siRNA联合阿霉素可使HepG2、HeLa和K562/DOX细胞的半数抑制浓度(IC50)分别降低3.13、5.22和1.74倍。在存在STAT3-siRNA的情况下,HepG2、HeLa和K562/DOX细胞内阿霉素的蓄积分别增加了16.8%、12.87%和25.67%。在经STAT3-siRNA处理的HepG2、HeLa和K562/DOX细胞中观察到阿霉素诱导的细胞凋亡增强。结果表明,STAT3-siRNA可增强阿霉素对HepG2、HeLa和K562/DOX细胞的抗肿瘤活性。

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