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Quantitative Analysis of Merkel Cell Polyomavirus (Mcpyv) Genome in Non-Melanoma Skin Cancer and Normal Tumor Margins Publisher Pubmed



Hasanzadeh A1 ; Sadeghi F2 ; Kamrani G3 ; Mohammadi N4 ; Vosough Z3 ; Ranaee M3 ; Tabarraei A5 ; Yahyapour Y6
Authors
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Authors Affiliations
  1. 1. Department of Microbiology, Faculty of Medicine, Golestan University of Medical Sciences, Gorgan, Iran
  2. 2. Cellular and Molecular Biology Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran
  3. 3. Department of Pathology, Faculty of Medicine, Babol University of Medical Sciences, Babol, Iran
  4. 4. Department of Epidemiology and Biostatistics, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
  5. 5. Infectious Diseases Research Center, Golestan University of Medical Sciences, Gorgan, Iran
  6. 6. Infectious Diseases and Tropical Medicine Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran

Source: Brazilian Journal of Microbiology Published:2022


Abstract

Merkel cell polyomavirus (MCPyV) is the cause of approximately 80% of Merkel cell carcinomas (MCC). The common types of non-melanoma skin cancer (NMSC) including squamous cell carcinoma (SCC) and basal cell carcinoma (BCC) are histologically similar to MCC. In the present study, 58 NMSC formalin-fixed paraffin-embedded tissue (FFPE) samples including 12 SCC, 46 BCC, and 58 FFPE samples of adjacent non-tumoral margins as the control were included. Determination of large tumor antigens (LTAg) copy number was performed by qReal-Time PCR as a viral copy number per cell to elucidate MCPyV carcinogenic role in non-melanoma skin cancer. Out of 58 samples, 36 (62%) cancerous and 22 (37.9%) normal tumor margins were positive for MCPyV LTAg. Median copy numbers of MCPyV LTAg among all NMSC samples and non-tumoral margins were 0.308×10−2 and 0.269×10−3 copies per cell respectively (P=0.001). In addition, although the viral load in the majority of samples was detected to be lower than one copy per cell, in 4 BCC samples, a viral load higher than one LTAg copy per cell was detected. The present study revealed that the detection of higher levels of MCPyV LTAg viral load in some BCC and SCC samples may be correlated with the role of MCPyV in some cases of BCC and SCC skin cancer. © 2022, The Author(s) under exclusive licence to Sociedade Brasileira de Microbiologia.