Merkel Cell Polyomavirus in the Context of Oral Squamous Cell Carcinoma and Oral Potentially Malignant Disorders

Author:

Passerini Sara1ORCID,Babini Giulia1,Merenda Elisabetta2ORCID,Carletti Raffaella2,Scribano Daniela1ORCID,Rosa Luigi3ORCID,Conte Antonietta Lucia1,Moens Ugo4,Ottolenghi Livia5ORCID,Romeo Umberto5ORCID,Conte Maria Pia1ORCID,Di Gioia Cira Rosaria Tiziana2ORCID,Pietropaolo Valeria1ORCID

Affiliation:

1. Department of Public Health and Infectious Diseases, “Sapienza” University of Rome, 00185 Rome, Italy

2. Department of Radiological, Oncological and Pathological Science, “Sapienza” University of Rome, 00161 Rome, Italy

3. Laboratory of Virology, National Institute for Infectious Diseases “Spallanzani”, 00149 Rome, Italy

4. Department of Medical Biology, Faculty of Health Sciences, University of Tromsø, UiT-The Arctic University of Norway, 9037 Tromsø, Norway

5. Department of Oral and Maxillofacial Sciences, Sapienza University of Rome, Via Caserta 6, 00161 Rome, Italy

Abstract

Despite recent advances in prevention, detection and treatment, oral squamous cell carcinoma (OSCC) remains a global health concern, strongly associated with environmental and lifestyle risk factors and infection with oncogenic viruses. Merkel Cell Polyomavirus (MCPyV), well known to be the causative agent of Merkel Cell Carcinoma (MCC) has been found in OSCC, suggesting its potential role as a co-factor in the development of oral cavity cancers. To improve our understanding about MCPyV in oral cavities, the detection and analysis of MCPyV DNA, transcripts and miRNA were performed on OSCCs and oral potentially malignant disorders (OPMDs). In addition, the cellular miR-375, known to be deregulated in tumors, was examined. MCPyV DNA was found in 3 out of 11 OSCC and 4 out of 12 OPMD samples, with a viral mean value of 1.49 × 102 copies/mL. Viral integration was not observed and LTAg and VP1 transcripts were detected. Viral miRNAs were not detected whereas the cellular miR-375 was found over expressed in all MCPyV positive oral specimens. Our results reported evidence of MCPyV replication in both OSCC and OPMD suggesting the oral cavity as a site of replicative MCPyV infection, therefore underscoring an active role of this virus in the occurrence of oral lesions.

Funder

MIUR Research

Publisher

MDPI AG

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