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Docosahexaenoic acid induces the degradation of HPV E6/E7 oncoproteins by activating the ubiquitin–proteasome system

机译:二十二碳六烯酸通过激活泛素-蛋白酶体系统诱导HPV E6 / E7癌蛋白降解。

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摘要

The oncogenic human papillomavirus (HPV) E6/E7 proteins are essential for the onset and maintenance of HPV-associated malignancies. Here, we report that activation of the cellular ubiquitin–proteasome system (UPS) by the omega-3 fatty acid, docosahexaenoic acid (DHA), leads to proteasome-mediated degradation of E6/E7 viral proteins and the induction of apoptosis in HPV-infected cancer cells. The increases in UPS activity and degradation of E6/E7 oncoproteins were associated with DHA-induced overproduction of mitochondrial reactive oxygen species (ROS). Exogenous oxidative stress and pharmacological induction of mitochondrial ROS showed effects similar to those of DHA, and inhibition of ROS production abolished UPS activation, E6/E7 viral protein destabilization, and apoptosis. These findings identify a novel role for DHA in the regulation of UPS and viral proteins, and provide evidence for the use of DHA as a mechanistically unique anticancer agent for the chemoprevention and treatment of HPV-associated tumors.
机译:致癌性人乳头瘤病毒(HPV)E6 / E7蛋白对于与HPV相关的恶性肿瘤的发作和维持至关重要。在这里,我们报告说,ω3脂肪酸二十二碳六烯酸(DHA)对细胞泛素-蛋白酶体系统(UPS)的激活导致蛋白酶体介导的E6 / E7病毒蛋白降解以及HPV-诱导细胞凋亡。被感染的癌细胞。 UPS活性的增加和E6 / E7癌蛋白的降解与DHA诱导的线粒体活性氧(ROS)过量产生有关。线粒体ROS的外源性氧化应激和药理作用显示出与DHA相似的效果,并且对ROS产生的抑制作用消除了UPS活化,E6 / E7病毒蛋白不稳定和细胞凋亡。这些发现确定了DHA在调节UPS和病毒蛋白中的新作用,并提供了将DHA用作化学预防和治疗HPV相关肿瘤的机制独特的抗癌剂的证据。

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