Ebrahimi Fatemeh, Modaresi Movahedi Ali, Sabbaghian Mohammad, Poortahmasebi Vahdat
Department of Bacteriology and Virology Faculty of Medical Sciences, Tabriz University of Medical Sciences Tabriz Iran.
Department of Medical Parasitology and Mycology Faculty of Medical Sciences, Shahid Sadoughi University of Medical Sciences Yazd Iran.
Health Sci Rep. 2024 Nov 18;7(11):e70196. doi: 10.1002/hsr2.70196. eCollection 2024 Nov.
Oncogenic viruses are responsible for approximately 12% of human malignancies, influencing various cancer processes through intricate interactions with host cells. Exosomes (EXOs), nanometric-sized microvesicles involved in cell communication, have emerged as critical mediators in these interactions. This review aims to explore the mechanisms by which EXOs produced by cells infected with oncogenic viruses promote cancer growth, enhance viral transmissibility, and act as immunomodulators.
A comprehensive review was conducted, focusing on recent studies highlighting the mechanisms by which EXOs facilitate the oncogenic potential of viruses. The analysis included the characterization of exosomal content, such as microRNAs (miRNAs) and proteins, and their effects on tumor microenvironments and immune responses. A search was performed using databases including PubMed, ScienceDirect, and Google Scholar. MeSH keywords related to EXOs, oncogenic viruses, and cancer were used to retrieve relevant review, systematic, and research articles.
Findings indicate that EXOs from oncogenic virus-infected cells carry viral components that facilitate infection and inflammation. These EXOs alter the tumor microenvironment, contributing to the development of virus-associated cancers. Additionally, the review highlights the growing interest among researchers regarding the implications of EXOs in cancer progression and their potential role in enhancing the oncogenicity of viruses.
The findings underscore the pivotal role of EXOs in mediating the oncogenic effects of viruses, suggesting that targeting exosomal pathways may provide new therapeutic avenues for managing virus-associated cancers. Further research is needed to fully elucidate the functional mechanisms of EXOs in viral oncogenesis.
致癌病毒约占人类恶性肿瘤的12%,通过与宿主细胞的复杂相互作用影响各种癌症进程。外泌体(EXOs)是参与细胞通讯的纳米级微泡,已成为这些相互作用中的关键介质。本综述旨在探讨感染致癌病毒的细胞产生的外泌体促进癌症生长、增强病毒传播性并作为免疫调节剂的机制。
进行了一项全面综述,重点关注近期突出外泌体促进病毒致癌潜力机制的研究。分析包括外泌体内容物(如微小RNA(miRNA)和蛋白质)的特征及其对肿瘤微环境和免疫反应的影响。使用包括PubMed、ScienceDirect和谷歌学术在内的数据库进行检索。使用与外泌体、致癌病毒和癌症相关的医学主题词(MeSH)检索相关综述、系统评价和研究文章。
研究结果表明,来自致癌病毒感染细胞的外泌体携带促进感染和炎症的病毒成分。这些外泌体改变肿瘤微环境,促进病毒相关癌症的发展。此外,该综述强调了研究人员对外泌体在癌症进展中的影响及其在增强病毒致癌性方面潜在作用的兴趣日益浓厚。
这些发现强调了外泌体在介导病毒致癌作用中的关键作用,表明靶向外泌体途径可能为治疗病毒相关癌症提供新的治疗途径。需要进一步研究以充分阐明外泌体在病毒致癌过程中的功能机制。