Epidemiology, biology and therapy of Merkel cell carcinoma: conclusions from the EU project IMMOMEC.
Jürgen Christian BeckerAndreas StangAxel Zur HausenNicole FischerJames A DeCaprioRichard W TothillRikke LyngaaUlla Kring HansenCathrin RitterPaul NghiemChristopher K BichakjianSelma UgurelDavid SchramaPublished in: Cancer immunology, immunotherapy : CII (2017)
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.
Keyphrases
- cell cycle
- signaling pathway
- risk factors
- high glucose
- diabetic rats
- quality improvement
- cell proliferation
- healthcare
- cell therapy
- single cell
- drug induced
- gene expression
- mesenchymal stem cells
- endothelial cells
- oxidative stress
- epithelial mesenchymal transition
- stem cells
- young adults
- endoplasmic reticulum stress
- induced apoptosis
- stress induced