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阐明芦丁通过下调 HPV-E6 和 E7 诱导宫颈癌 HeLa 细胞 caspase 依赖性凋亡的作用。

Elucidation of rutin's role in inducing caspase-dependent apoptosis via HPV-E6 and E7 down-regulation in cervical cancer HeLa cells.

机构信息

Department of Biotechnology, Noida Institute of Engineering and Technology, Greater Noida 201306, India.

Department of Basic Sciences, King Faisal University, Al Ahsa 31982, Kingdom of Saudi Arabia.

出版信息

Biosci Rep. 2021 Jun 25;41(6). doi: 10.1042/BSR20210670.

Abstract

Over the recent few years rutin has gained wider attention in exhibiting inhibitory potential against several oncotargets for inducing apoptotic and antiproliferative activity in several human cancer cells. Several deregulated signaling pathways are implicated in cancer pathogenesis. Therefore we have inclined our research towards exploring the anticancerous efficacy of a very potent phytocompound for modulating the incontinent expression of these two crucial E6 and E7 oncogenes. Further, inhibitory efficacy of rutin against human papillomavirus (HPV)-E6 and E7 oncoproteins in cervical cancer has not been elucidated yet. This research addresses the growth inhibitory efficacy of rutin against E6 and E7 oncoproteins in HeLa cells, which is known to inactivate several tumor suppressor proteins such as p53 and pRB. Rutin treatment exhibited reduced cell viability with increased cell accumulation in G0/G1 phase of cell cycle in HeLa cell lines. Additionally, rutin treatment has also led to down-regulation of E6 and E7 expression associated with an increased expression of p53 and pRB levels. This has further resulted in enhanced Bax expression and decreased Bcl-2 expression releasing cytochrome c into cytosol followed by caspase cascade activation with cleavage of caspase-3, caspase-8 and caspase-9. Further, in silico studies have also supported our in vitro findings by exhibiting significant binding energy against selected target oncoproteins. Therefore, our research findings might recommend rutin as one of the potent drug candidate in cervical cancer management via targeting two crucial oncoproteins associated with viral progression.

摘要

在最近几年,芦丁作为一种潜在的抑制剂,对多种人类癌细胞中的凋亡和抗增殖活性的多个肿瘤靶点表现出抑制作用,引起了广泛关注。有几种失调的信号通路被认为与癌症的发病机制有关。因此,我们的研究倾向于探索一种非常有效的植物化合物的抗癌功效,以调节这两种关键的 E6 和 E7 致癌基因的失控表达。此外,芦丁对人乳头瘤病毒(HPV)-E6 和 E7 致癌蛋白在宫颈癌中的抑制作用尚未阐明。本研究旨在探讨芦丁对 HeLa 细胞中 E6 和 E7 致癌蛋白的生长抑制作用,已知 E6 和 E7 致癌蛋白可使几种肿瘤抑制蛋白如 p53 和 pRB 失活。芦丁处理表现出细胞活力降低,细胞周期 G0/G1 期细胞积累增加。此外,芦丁处理还导致 E6 和 E7 表达下调,同时 p53 和 pRB 水平上调。这进一步导致 Bax 表达增加,Bcl-2 表达减少,细胞色素 c 释放到细胞质中,随后 caspase 级联激活,caspase-3、caspase-8 和 caspase-9 被切割。此外,计算机模拟研究也通过对选定的靶标致癌蛋白表现出显著的结合能,支持了我们的体外研究结果。因此,我们的研究结果可能建议芦丁作为一种通过靶向与病毒进展相关的两个关键致癌蛋白的宫颈癌治疗的潜在候选药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc85/8220446/f37240422f31/bsr-41-bsr20210670-g1.jpg

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