Key result
Merkel cell polyomavirus DNA shows no difference in prevalence between malignant and non-malignant oral lesions.
Why the study?
Infection with human tumor viruses is a hypothesized cause of cancer, motivating the exploration and quantification of Merkel cell polyomavirus in oral cavity lesions in Northern Iran.
Cross-Sectional (n=114)
No
Absolute Event Rate: 20.4% vs 27.7%
p-value: p=0.471
Merkel cell polyomavirus (MCPyV) DNA is present in a proportion of various oral cavity lesions in Northern Iran, suggesting a potential role in their occurrence.
MCPyV detection in oral lesions warrants no clinical action now; leaves open any etiologic role in Iranian patients.
OBJECTIVE: Infection with human tumor viruses is one of the hypothesized causes of cancer. The current investigation aimed to explore the presence and quantitative analysis of a new human tumor virus, Merkel cell polyomavirus (MCPyV) in tissue samples of 114 patients with oral cavity lesions including oral squamous cell carcinoma (OSCC), oral lichen planus (OLP), Dysplasia and oral irritation fibroma (OIF) in Northern Iran. METHODS: From 114 formalin fixed paraffin embedded samples; 35 with SCC, 29 with OLP, 14 with dysplasia and 36 with OIF were cut, deparaffinized and DNA was extracted. Quantitative detection of MCPyV large T antigen was performed by absolute quantitative Real-Time PCR. RESULT: MCPyV DNA was detected in 30.6% (n: 11/36) of IF, 24.1% (n; 7/29) of OLP, 21.4% (n:3/14) of dysplasia and 20% (n;7/35) of OSCC samples. The mean MCPyV DNA copy number was 2.32×10-2 ± 3.97 ×10-2, 2.02×10-2 (SD=3.13×10-2), 2.69×10-4 (SD=2.51×10-4), and 2.56×10-4 (SD=6.73×10-4) per cell in OSCC, dysplasia and both of OLP and OIF samples, respectively (P=0.76). CONCLUSION: This study provides the first data from Iran regarding the presence of MCPyV genome in oral cavity lesions and oral cancer. These results also emphasize that MCPyV has an active role in the occurrence of oral lesions and progression to cancer. Further studies should be carried out to clarify the role of MCPyV in oral cavity lesions.
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Estalkhi et al. (2021) conducted a cross-sectional in Oral cavity lesions (n=114). Merkel cell polyomavirus (MCPyV) infection vs. Non-malignant oral lesions was evaluated on Presence of MCPyV genome in malignant/premalignant vs non-malignant samples (p=0.471). Merkel cell polyomavirus DNA was detected in 24.6% of oral cavity biopsies overall, with no significant difference in prevalence between malignant/premalignant (20.4%) and non-malignant (27.7%) lesions.
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