The Distinctive Mutational Spectra of Polyomavirus-Negative Merkel Cell Carcinoma

Paul W. Harms(University of Michigan), Pankaj Vats(Bharathidasan University), Monique Verhaegen(University of Michigan), Dan R. Robinson(Michigan Center for Translational Pathology), Yi-Mi Wu(University of Michigan), Saravana M. Dhanasekaran(University of Michigan), Nallasivam Palanisamy(Henry Ford Health System), Javed Siddiqui(University of Michigan), Xuhong Cao(Howard Hughes Medical Institute), Fengyun Su(Michigan Center for Translational Pathology), Rui Wang(University of Michigan), Hong Xiao(Henry Ford Health System), Lakshmi P. Kunju(University of Michigan), Rohit Mehra(Henry Ford Health System), Scott A. Tomlins(University of Michigan), Douglas R. Fullen(University of Michigan), Christopher K. Bichakjian(University of Michigan), Timothy M. Johnson(University of Michigan), Andrzej A. Dlugosz(University of Michigan), Arul M. Chinnaiyan(Howard Hughes Medical Institute)
Cancer Research
August 3, 2015
Cited by 340Open Access
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Abstract

Merkel cell carcinoma (MCC) is a rare but highly aggressive cutaneous neuroendocrine tumor. Merkel cell polyomavirus (MCPyV) may contribute to tumorigenesis in a subset of tumors via inhibition of tumor suppressors such as retinoblastoma (RB1) by mutated viral T antigens, but the molecular pathogenesis of MCPyV-negative MCC is largely unexplored. Through our MI-ONCOSEQ precision oncology study, we performed integrative sequencing on two cases of MCPyV-negative MCC, as well as a validation cohort of 14 additional MCC cases (n = 16). In addition to previously identified mutations in TP53, RB1, and PIK3CA, we discovered activating mutations of oncogenes, including HRAS and loss-of-function mutations in PRUNE2 and NOTCH family genes in MCPyV-negative MCC. MCPyV-negative tumors also displayed high overall mutation burden (10.09 ± 2.32 mutations/Mb) and were characterized by a prominent UV-signature pattern with C > T transitions comprising 85% of mutations. In contrast, mutation burden was low in MCPyV-positive tumors (0.40 ± 0.09 mutations/Mb) and lacked a UV signature. These findings suggest a potential ontologic dichotomy in MCC, characterized by either viral-dependent or UV-dependent tumorigenic pathways.


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