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miR-187 induces apoptosis of SiHa cervical carcinoma cells by downregulating Bcl-2

机译:miR-187通过下调Bcl-2诱导SiHa宫颈癌细胞凋亡

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Cervical carcinoma is a life-threatening illness posing considerable danger to women’s health. microRNAs (miRNAs) have been shown to regulate multiple cellular events, including growth and proliferation, and miR-187 is thought to regulate the growth and apoptosis of certain cell types. Our study focused on the influence of miR-187 on the growth, proliferation, and apoptosis of SiHa cervical carcinoma cells, and explored the mechanism behind its pro-apoptotic effect. miR-187 and control (scrambled) miRNA were synthesized with a standard protocol and lipofected into SiHa cells. Thiazolyl blue tetrazolium bromide assays and tests of caspase-3 activity were then performed to examine growth, proliferation, and apoptosis by flow cytometry. Small interfering RNA (siRNA) and an expression plasmid were synthesized for inhibition and overexpression of Bcl-2, respectively, and following their transfection, western blotting was used to examine Bcl-2 protein levels. Compared to transfection with control miRNA, miR-187 significantly reduced SiHa cell growth and decreased Bcl-2 expression. Increased translocation of phosphatidylserine and activation of caspase-3 were observed in miR-187-transfected cells. Moreover, inhibition of Bcl-2 enhanced the pro-apoptotic effect of this miRNA, while Bcl-2 overexpression had the opposite effect. miR-187 inhibits the growth and proliferation of SiHa cells, and induces their apoptosis via downregulation of Bcl-2. Bcl-2 represents a potential therapeutic target for cervical carcinoma.
机译:宫颈癌是威胁生命的疾病,对妇女的健康构成极大威胁。 microRNA(miRNA)已被证明可以调节多种细胞事件,包括生长和增殖,而miR-187被认为可以调节某些细胞类型的生长和凋亡。我们的研究集中于miR-187对SiHa宫颈癌细胞的生长,增殖和凋亡的影响,并探索其促凋亡作用的机制。用标准方案合成了miR-187和对照(加扰的)miRNA,并脂转染到SiHa细胞中。然后进行了噻唑蓝溴化四唑鎓测定和caspase-3活性测试,以通过流式细胞术检查生长,增殖和凋亡。分别合成了小干扰RNA(siRNA)和表达质粒分别用于抑制和过度表达Bcl-2,转染后,使用western blotting检测Bcl-2蛋白的水平。与对照miRNA转染相比,miR-187显着降低了SiHa细胞的生长,并降低了Bcl-2的表达。在miR-187转染的细胞中观察到磷脂酰丝氨酸的转运增加和caspase-3的激活。而且,抑制Bcl-2增强了该miRNA的促凋亡作用,而Bcl-2过表达则具有相反的作用。 miR-187抑制SiHa细胞的生长和增殖,并通过下调Bcl-2诱导其凋亡。 Bcl-2代表宫颈癌的潜在治疗靶标。

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