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病毒致癌作用的最新研究进展:现有预防和治疗实体。

Recent Updates on Viral Oncogenesis: Available Preventive and Therapeutic Entities.

机构信息

Department of Industrial Microbiology, Sam Higginbottom University of Agriculture, Technology and Sciences, Prayagraj 211007, Uttar Pradesh India.

Department of Bioengineering and Biotechnology, Birla Institute of Technology, Mesra, Ranchi 835215, Jharkhand, India.

出版信息

Mol Pharm. 2023 Aug 7;20(8):3698-3740. doi: 10.1021/acs.molpharmaceut.2c01080. Epub 2023 Jul 24.

Abstract

Human viral oncogenesis is a complex phenomenon and a major contributor to the global cancer burden. Several recent findings revealed cellular and molecular pathways that promote the development and initiation of malignancy when viruses cause an infection. Even, antiviral treatment has become an approach to eliminate the viral infections and prevent the activation of oncogenesis. Therefore, for a better understanding, the molecular pathogenesis of various oncogenic viruses like, hepatitis virus, human immunodeficiency viral (HIV), human papillomavirus (HPV), herpes simplex virus (HSV), and Epstein-Barr virus (EBV), could be explored, especially, to expand many potent antivirals that may escalate the apoptosis of infected malignant cells while sparing normal and healthy ones. Moreover, contemporary therapies, such as engineered antibodies antiviral agents targeting signaling pathways and cell biomarkers, could inhibit viral oncogenesis. This review elaborates the recent advancements in both natural and synthetic antivirals to control viral oncogenesis. The study also highlights the challenges and future perspectives of using antivirals in viral oncogenesis.

摘要

人类病毒致癌是一种复杂的现象,也是导致全球癌症负担的主要因素之一。最近的一些发现揭示了细胞和分子途径,当病毒引起感染时,这些途径会促进恶性肿瘤的发展和起始。即使是抗病毒治疗也已成为消除病毒感染和预防致癌作用的一种方法。因此,为了更好地理解,我们可以探索各种致癌病毒的分子发病机制,如肝炎病毒、人类免疫缺陷病毒 (HIV)、人乳头瘤病毒 (HPV)、单纯疱疹病毒 (HSV) 和爱泼斯坦-巴尔病毒 (EBV),特别是要开发许多有效的抗病毒药物,这些药物可能会在不损伤正常和健康细胞的情况下促进感染恶性细胞的凋亡。此外,当代疗法,如针对信号通路和细胞生物标志物的工程抗体抗病毒药物,也可以抑制病毒致癌。本文详细阐述了控制病毒致癌的天然和合成抗病毒药物的最新进展。该研究还强调了在病毒致癌中使用抗病毒药物的挑战和未来展望。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73ab/10410670/d6e5c96d3954/mp2c01080_0001.jpg

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