| Literature DB >> 31759946 |
Thibault Kervarrec1, Mohanad Aljundi2, Silke Appenzeller3, Mahtab Samimi4, Eve Maubec2, Bernard Cribier5, Lydia Deschamps6, Bhavishya Sarma7, Eva-Maria Sarosi7, Patricia Berthon8, Annie Levy9, Guilhem Bousquet10, Anne Tallet11, Antoine Touzé8, Serge Guyétant12, David Schrama7, Roland Houben7.
Abstract
Merkel cell carcinoma (MCC), an aggressive neuroendocrine carcinoma of the skin, is to date the only human cancer known to be frequently caused by a polyomavirus. However, it is a matter of debate which cells are targeted by the Merkel cell polyomavirus (MCPyV) to give rise to the phenotypically multifaceted MCC cells. To assess the lineage of origin of MCPyV-positive MCC, genetic analysis of a very rare tumor combining benign trichoblastoma and MCPyV-positive MCC was conducted by massive parallel sequencing. Although MCPyV was found to be integrated only in the MCC part, six somatic mutations were shared by both tumor components. The mutational overlap between the trichoblastoma and MCPyV-positive MCC parts of the combined tumor implies that MCPyV integration occurred in an epithelial tumor cell before MCC development. Therefore, our report demonstrates that MCPyV-positive MCC can derive from the epithelial lineage.Entities:
Year: 2019 PMID: 31759946 DOI: 10.1016/j.jid.2019.09.026
Source DB: PubMed Journal: J Invest Dermatol ISSN: 0022-202X Impact factor: 8.551