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Binase treatment increases interferon sensitivity and apoptosis in SiHa cervical carcinoma cells by downregulating E6 and E7 human papilloma virus oncoproteins

机译:Binase处理可通过下调E6和E7人乳头瘤病毒癌蛋白来增加SiHa宫颈癌细胞的干扰素敏感性和细胞凋亡

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摘要

In this study, we determined whether binase, a ribonuclease from Bacillus pumilus, increases interferon sensitivity and apoptosis in SiHa cervical cancer cells infected with high-risk human papilloma virus (HPV) strain 16. Binase treatment increased SiHa cell apoptosis in a time- and concentration-dependent manner, as determined by flow cytometry, WST tests and real time xCelligence cell index analysis. Binase-treated SiHa cells showed reduced expression of E6 and E7 viral oncoproteins and increased expression of their intracellular targets, p53 and pRb. Combined treatment with binase and IFNα2b enhanced the interferon sensitivity of HPV-positive SiHa cells. By contrast, combined treatment with binase and IFNα2b in HPV-negative C33A cervical cancer cells, which do no expess E6 and E7, elicited no changes in interferon sensitivity or p53 and pRb expression. These findings suggest binase enhances interferon sensitivity and apoptosis in HPV-positive SiHa cervical cancer cells by suppressing E6 and E7 viral protein expression.
机译:在这项研究中,我们确定Binase(一种来自短小芽孢杆菌的核糖核酸酶)是否增加了感染高危人乳头瘤病毒(HPV)菌株16的SiHa宫颈癌细胞中的干扰素敏感性和细胞凋亡。通过流式细胞仪,WST测试和实时xCelligence细胞指数分析确定的浓度依赖性方式。用Binase处理的SiHa细胞显示E6和E7病毒癌蛋白的表达减少,并且其细胞内靶标p53和pRb的表达增加。 Binase和IFNα2b的联合处理增强了HPV阳性SiHa细胞的干扰素敏感性。相比之下,在没有花费E6和E7的HPV阴性C33A宫颈癌细胞中,用Binase和IFNα2b联合治疗不会引起干扰素敏感性或p53和pRb表达的变化。这些发现表明,二合酶可以通过抑制E6和E7病毒蛋白表达来增强HPV阳性SiHa宫颈癌细胞中的干扰素敏感性和细胞凋亡。

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