| Literature DB >> 29188306 |
Jürgen C Becker1,2,3, Andreas Stang4,5, Axel Zur Hausen6, Nicole Fischer7, James A DeCaprio8, Richard W Tothill9, Rikke Lyngaa10, Ulla Kring Hansen11, Cathrin Ritter12,4, Paul Nghiem11, Christopher K Bichakjian13, Selma Ugurel14, David Schrama15.
Abstract
Merkel cell carcinoma (MCC) is a highly aggressive, often lethal neuroendocrine cancer. Its carcinogenesis may be either caused by the clonal integration of the Merkel cell polyomavirus into the host genome or by UV-induced mutations. Notably, virally-encoded oncoproteins and UV-induced mutations affect comparable signaling pathways such as RB restriction of cell cycle progression or p53 inactivation. Despite its low incidence, MCC recently received much attention based on its exquisite immunogenicity and the resulting major success of immune modulating therapies. Here, we summarize current knowledge on epidemiology, biology and therapy of MCC as conclusion of the project 'Immune Modulating strategies for treatment of Merkel Cell Carcinoma', which was funded over a 5-year period by the European Commission to investigate innovative immunotherapies for MCC.Entities:
Keywords: Cell of origin; Epidemiology; IMMOMEC; Immunotherapy; Merkel cell carcinoma; Merkel cell polyomavirus
Mesh:
Year: 2017 PMID: 29188306 PMCID: PMC6015651 DOI: 10.1007/s00262-017-2099-3
Source DB: PubMed Journal: Cancer Immunol Immunother ISSN: 0340-7004 Impact factor: 6.968