Merkel Cell Polyomavirus-Pathophysiology and Treatment in the Era of Gene-Targeted Therapies.

Rev Med Virol

Institute of Biomedicine and Glycomics and School and Pharmacy and Medical Sciences, Griffith University, Gold Coast, Australia.

Published: September 2024

AI Article Synopsis

  • Merkel cell polyomavirus (MCPyV) is a key factor in causing Merkel cell carcinoma (MCC), a deadly skin cancer with a low survival rate and high recurrence.
  • Current treatments for MCC are often ineffective, especially for metastatic cases, creating a pressing need for new therapeutic options.
  • Gene-targeted therapies like siRNA and CRISPR/Cas hold potential for MCC treatment, but more research and clinical trials are needed to translate these strategies into effective solutions.

Article Abstract

Merkel cell polyomavirus (MCPyV) is a significant contributor to the development of Merkel cell carcinoma (MCC), an aggressive skin cancer with high recurrence and a low survival rate. In fact, it is the deadliest skin cancer. The precise routes of transmission for MCPyV-positive MCC remain unclear, but several factors may trigger its development. Conventional treatments for MCC are not highly effective, especially in patients with metastasis, with a clear need for new treatment options. Gene-targeted therapies hold great promise for the treatment of MCC, including the use of siRNA and CRISPR/Cas (C/Cas) but critically none have yet been translated into clinical trials. Validating this approach is the fact that several siRNA products are already FDA licenced, while C/Cas has entered clinical trial, albeit for conditions other than MCC. There are many challenges that must be overcome to move from preclinical research to the clinic. In this review, we provide a comprehensive summary of the current understanding of MCC, with a particular focus on MCPyV-positive MCC, and the status of gene-targeted therapies. Additionally, we discuss the major obstacles that impede MCC research and explore future prospects.

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Source
http://dx.doi.org/10.1002/rmv.2580DOI Listing

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