是否还有更多人类癌症病毒有待发现?

IF 8.1 1区 医学 Q1 VIROLOGY Annual Review of Virology Pub Date : 2024-09-01 DOI:10.1146/annurev-virology-111821-103721
Patrick S Moore, Yuan Chang
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引用次数: 0

摘要

在感染人类的数千种病毒中,只有七种会导致普通人群患癌。目前,肿瘤测序已成为一种常见的癌症医学程序,因此,如果有更多的人类癌症病毒存在,很可能已经被发现。在此,我们回顾了可为专门寻找新癌症病毒提供信息的癌症特征,重点介绍了卡波西肉瘤疱疹病毒和梅克尔细胞多瘤病毒,它们是基因组和转录组搜索成功的最新范例。我们强调流行病学在确定检查哪些癌症方面的重要性,并介绍了发现病毒的方法。发现病毒的障碍可能存在,例如新基因组和病毒对信使 RNA 表达的抑制,这些障碍阻碍了利用现有方法发现病毒。最理想的病毒猎杀方式是,如果没有发现病毒,则可以合理地排除肿瘤的感染病因,并发现有关肿瘤生物学的新信息。
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Are There More Human Cancer Viruses Left to Be Found?

Of the thousands of viruses infecting humans, only seven cause cancer in the general population. Tumor sequencing is now a common cancer medicine procedure, and so it seems likely that more human cancer viruses already would have been found if they exist. Here, we review cancer characteristics that can inform a dedicated search for new cancer viruses, focusing on Kaposi sarcoma herpesvirus and Merkel cell polyomavirus as the most recent examples of successful genomic and transcriptomic searches. We emphasize the importance of epidemiology in determining which cancers to examine and describe approaches to virus discovery. Barriers to virus discovery, such as novel genomes and viral suppression of messenger RNA expression, may exist that prevent virus discovery using existing approaches. Optimally virus hunting should be performed in such a way that if no virus is found, the tumor can be reasonably excluded from having an infectious etiology and new information about the biology of the tumor can be found.

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来源期刊
CiteScore
19.40
自引率
0.90%
发文量
28
期刊介绍: The Annual Review of Virology serves as a conduit for disseminating thrilling advancements in our comprehension of viruses spanning animals, plants, bacteria, archaea, fungi, and protozoa. Its reviews illuminate novel concepts and trajectories in basic virology, elucidating viral disease mechanisms, exploring virus-host interactions, and scrutinizing cellular and immune responses to virus infection. These reviews underscore the exceptional capacity of viruses as potent probes for investigating cellular function.
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