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人乳头瘤病毒 16 型 E5 癌蛋白作为宫颈癌治疗的新靶点。

Human papillomavirus type 16 E5 oncoprotein as a new target for cervical cancer treatment.

机构信息

Department of Obstetrics and Gynecology, Seoul National University College of Medicine, Seoul, Republic of Korea.

出版信息

Biochem Pharmacol. 2010 Dec 15;80(12):1930-5. doi: 10.1016/j.bcp.2010.07.013. Epub 2010 Jul 17.

Abstract

Human papillomavirus (HPV) infection is considered to be the necessary cause of cervical cancer. E6 and E7 oncoproteins of HPV have been known to play major roles in malignant transformation of cervical cells, inhibiting the tumor suppressors p53 and Rb. However, the role of E5 oncoprotein has been relatively less defined. HPV 16 E5 is a hydrophobic membrane-bound protein which associates with the Golgi apparatus, endoplasmic reticulum and perinuclear membrane. Accumulating evidences have suggested that E5 oncoprotein may also contribute to cervical carcinogenesis through modulating cellular signaling pathways in addition to augmenting the immortalization potential of E6 and E7. Multiple mechanisms, including activation of EGFR or inflammatory cell signaling pathway, have been implicated in malignant transformation by HPV 16 E5. Therefore, targeting E5 may be a rational approach for chemoprevention and treatment of cervical cancer, and understanding its oncogenic processes may help us to design novel therapeutic strategies. In this review, we discussed the roles of HPV 16 E5 in cervical carcinogenesis, altering several cellular signaling pathways involved in cell proliferation, angiogenesis and apoptosis.

摘要

人乳头瘤病毒(HPV)感染被认为是宫颈癌的必要病因。HPV 的 E6 和 E7 癌蛋白已被证实主要在宫颈细胞的恶性转化中发挥作用,抑制肿瘤抑制因子 p53 和 Rb。然而,E5 癌蛋白的作用相对较少被定义。HPV 16 E5 是一种疏水的膜结合蛋白,与高尔基体、内质网和核周膜相关。越来越多的证据表明,E5 癌蛋白除了增强 E6 和 E7 的永生化潜力外,还可能通过调节细胞信号通路促进宫颈癌的发生。包括激活 EGFR 或炎症细胞信号通路在内的多种机制已被牵涉到 HPV 16 E5 的恶性转化中。因此,针对 E5 可能是预防和治疗宫颈癌的合理方法,了解其致癌过程可能有助于我们设计新的治疗策略。在这篇综述中,我们讨论了 HPV 16 E5 在宫颈癌发生中的作用,改变了涉及细胞增殖、血管生成和细胞凋亡的几种细胞信号通路。

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