From Merkel Cell Polyomavirus Infection to Merkel Cell Carcinoma Oncogenesis

Merkel cell polyomavirus (MCPyV) infection causes near-ubiquitous, asymptomatic infection in the skin, but occasionally leads to an aggressive skin cancer called Merkel cell carcinoma (MCC). Epidemiological evidence suggests that poorly controlled MCPyV infection may be a precursor to MCPyV-associat...

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Main Authors: Nathan A. Krump, Jianxin You
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-09-01
Series:Frontiers in Microbiology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fmicb.2021.739695/full
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author Nathan A. Krump
Jianxin You
author_facet Nathan A. Krump
Jianxin You
author_sort Nathan A. Krump
collection DOAJ
description Merkel cell polyomavirus (MCPyV) infection causes near-ubiquitous, asymptomatic infection in the skin, but occasionally leads to an aggressive skin cancer called Merkel cell carcinoma (MCC). Epidemiological evidence suggests that poorly controlled MCPyV infection may be a precursor to MCPyV-associated MCC. Clearer understanding of host responses that normally control MCPyV infection could inform prophylactic measures in at-risk groups. Similarly, the presence of MCPyV in most MCCs could imbue them with vulnerabilities that-if better characterized-could yield targeted intervention solutions for metastatic MCC cases. In this review, we discuss recent developments in elucidating the interplay between host cells and MCPyV within the context of viral infection and MCC oncogenesis. We also propose a model in which insufficient restriction of MCPyV infection in aging and chronically UV-damaged skin causes unbridled viral replication that licenses MCC tumorigenesis.
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spelling doaj.art-6c7f97ce0f0d4d519b914bddf528d9162022-12-21T21:26:03ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2021-09-011210.3389/fmicb.2021.739695739695From Merkel Cell Polyomavirus Infection to Merkel Cell Carcinoma OncogenesisNathan A. KrumpJianxin YouMerkel cell polyomavirus (MCPyV) infection causes near-ubiquitous, asymptomatic infection in the skin, but occasionally leads to an aggressive skin cancer called Merkel cell carcinoma (MCC). Epidemiological evidence suggests that poorly controlled MCPyV infection may be a precursor to MCPyV-associated MCC. Clearer understanding of host responses that normally control MCPyV infection could inform prophylactic measures in at-risk groups. Similarly, the presence of MCPyV in most MCCs could imbue them with vulnerabilities that-if better characterized-could yield targeted intervention solutions for metastatic MCC cases. In this review, we discuss recent developments in elucidating the interplay between host cells and MCPyV within the context of viral infection and MCC oncogenesis. We also propose a model in which insufficient restriction of MCPyV infection in aging and chronically UV-damaged skin causes unbridled viral replication that licenses MCC tumorigenesis.https://www.frontiersin.org/articles/10.3389/fmicb.2021.739695/fullMerkel cell polyomavirusMerkel cell carcinomapersistenceinnate immune responseintegrationdysbiosis
spellingShingle Nathan A. Krump
Jianxin You
From Merkel Cell Polyomavirus Infection to Merkel Cell Carcinoma Oncogenesis
Frontiers in Microbiology
Merkel cell polyomavirus
Merkel cell carcinoma
persistence
innate immune response
integration
dysbiosis
title From Merkel Cell Polyomavirus Infection to Merkel Cell Carcinoma Oncogenesis
title_full From Merkel Cell Polyomavirus Infection to Merkel Cell Carcinoma Oncogenesis
title_fullStr From Merkel Cell Polyomavirus Infection to Merkel Cell Carcinoma Oncogenesis
title_full_unstemmed From Merkel Cell Polyomavirus Infection to Merkel Cell Carcinoma Oncogenesis
title_short From Merkel Cell Polyomavirus Infection to Merkel Cell Carcinoma Oncogenesis
title_sort from merkel cell polyomavirus infection to merkel cell carcinoma oncogenesis
topic Merkel cell polyomavirus
Merkel cell carcinoma
persistence
innate immune response
integration
dysbiosis
url https://www.frontiersin.org/articles/10.3389/fmicb.2021.739695/full
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