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Merkel cell polyomavirus and non-Merkel cell carcinomas: guilty or circumstantial evidence?

Merkel细胞多瘤病毒和非Merkel细胞癌: 有罪还是间接证据?

  • 影响因子:1.98
  • DOI:10.1111/apm.13019
  • 作者列表:"Csoboz B","Rasheed K","Sveinbjørnsson B","Moens U
  • 发表时间:2020-02-01
Abstract

:Merkel cell polyomavirus (MCPyV) is the major causative factor of the rare but aggressive cancer, Merkel cell carcinoma (MCC). Two characteristics of MCPyV-positive MCCs are integration of the viral genome and expression of a truncated version of one of its oncogenic proteins, namely large T antigen. The strong association of MCPyV with MCC development has incited researchers to further investigate a possible role of this virus in other cancers. However, many of the examples displaying the presence of the virus in the various non-MCC cancers are not able to clearly demonstrate a direct connection between cellular transformation and the presence of the virus. The prevalence of the virus is significantly lower in non-MCC cancers compared to MCCs, with a lower level of viral load and sparse viral protein expression. Moreover, the state of the viral genome, and whether a truncated large T antigen is expressed, has rarely been investigated. Nonetheless, considering the strong oncogenic potential of MCPyV proteins in MCC, the plausible contribution of MCPyV to transformation and cancer growth in non-MCC tumors cannot be ruled out. Furthermore, the absence of MCPyV in cancers does not exclude a hit-and-run mechanism, or the oncoproteins of MCPyV may potentiate the neoplastic process mediated by co-infecting oncoviruses such as high-risk human papillomaviruses and Epstein-Barr virus. The current review is focusing on the available data describing the presence of MCPyV in non-MCC tumors, with an aim to provide a comprehensive overview of the corresponding literature and to discuss the potential contribution of MCPyV to non-MCC cancer in light of this.

摘要

: Merkel细胞多瘤病毒 (MCPyV) 是罕见但侵袭性癌症Merkel细胞癌 (MCC) 的主要致病因素。MCPyV阳性MCCs的两个特征是病毒基因组的整合和其致癌蛋白之一即大T抗原的截短表达。MCPyV与MCC发展的强烈关联促使研究人员进一步调查这种病毒在其他癌症中的可能作用。然而,许多显示病毒存在于各种非MCC癌症中的例子不能清楚地证明细胞转化和病毒存在之间的直接联系。与MCCs相比,非MCC癌症中病毒的患病率显著较低,病毒载量较低,病毒蛋白表达稀疏。此外,病毒基因组的状态,以及是否表达截短的大T抗原,很少被研究。尽管如此,考虑到MCPyV蛋白在MCC中的强致癌潜力,不能排除MCPyV对非MCC肿瘤转化和癌症生长的合理贡献。此外,癌症中没有MCPyV并不排除肇事逃逸机制,或者MCPyV的癌蛋白可能通过共同感染onco病毒 (如高危型人乳头瘤病毒es和Epstein-Barr病毒) 介导的肿瘤形成过程。目前的综述集中在描述非MCC肿瘤中存在MCPyV的现有数据上,目的提供相应文献的全面概述,并据此讨论MCPyV对非MCC癌的潜在贡献。

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关键词: 暂无
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影响因子:2.93
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影响因子:0.96
发表时间:2020-01-01
DOI:10.1097/DAD.0000000000001459
作者列表:["Lang UE","Love NR","Cheung C","McCalmont TH","Kim J"]

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皮肤肿瘤方向

皮肤肿瘤是发生在皮肤的细胞增生性疾病,是一种常见病。发生于皮内或皮下组织的新生物,种类很多,临床上分良性肿瘤和恶性肿瘤。恶性肿瘤可以不断增殖,引起转移,威胁生命,称为皮肤癌。

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