人类多瘤病毒:大小肿瘤抗原之战。

Q1 Medicine
Virology: Research and Treatment Pub Date : 2017-12-05 eCollection Date: 2017-01-01 DOI:10.1177/1178122X17744785
Camila Freze Baez, Rafael Brandão Varella, Sonia Villani, Serena Delbue
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引用次数: 29

摘要

大约40年前,多瘤病毒(pyv)猴空泡病毒40的大抗原和小抗原(LT-Ag和sT-Ag)已被鉴定和表征。迄今为止,众所周知,所有发现的人类pyv (hpyv)编码这2种多功能致瘤蛋白,在病毒复制早期表达。这2种T-Ags在体内和体外都能转化细胞,似乎在人类某些肿瘤的发病机制中起着独特的作用。此外,它们还参与病毒DNA复制、转录和病毒粒子组装。本文简要介绍了hpyv的LT-Ag和sT-Ag的结构和功能特征,重点介绍了它们的转化特性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Human Polyomaviruses: The Battle of Large and Small Tumor Antigens.

Human Polyomaviruses: The Battle of Large and Small Tumor Antigens.

Human Polyomaviruses: The Battle of Large and Small Tumor Antigens.

Human Polyomaviruses: The Battle of Large and Small Tumor Antigens.

About 40 years ago, the large and small tumor antigens (LT-Ag and sT-Ag) of the polyomavirus (PyVs) simian vacuolating virus 40 have been identified and characterized. To date, it is well known that all the discovered human PyVs (HPyVs) encode these 2 multifunctional and tumorigenic proteins, expressed at viral replication early stage. The 2 T-Ags are able to transform cells both in vitro and in vivo and seem to play a distinct role in the pathogenesis of some tumors in humans. In addition, they are involved in viral DNA replication, transcription, and virion assembly. This short review focuses on the structural and functional features of the HPyVs' LT-Ag and sT-Ag, with special attention to their transforming properties.

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来源期刊
Virology: Research and Treatment
Virology: Research and Treatment Medicine-Infectious Diseases
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