Prevalence of Co-infection by Human Papillomavirus, Epstein- Barr Virus and Merkel Cell Polyomavirus in Iranian Oral Cavity Cancer and Pre-malignant Lesions.

IF 1.5 Q3 MEDICINE, RESEARCH & EXPERIMENTAL International Journal of Molecular and Cellular Medicine Pub Date : 2022-01-01 Epub Date: 2022-10-03 DOI:10.22088/IJMCM.BUMS.11.1.64
Sagahr Saber Amoli, Ali Hasanzadeh, Farzin Sadeghi, Mohammad Chehrazi, Maryam Seyedmajidi, Arghavan Zebardast, Yousef Yahyapour
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Abstract

Human papillomavirus (HPV) is recognized as the most important risk factor in oral cavity cancer and pre-malignant lesions; however, the etiological association of concomitant infection with other oncogenic viruses as a co-factor has not been definitively proven. The present study aimed to determine the prevalence of co-infection with HPV, Epstein-Barr virus (EBV) and Merkel Cell PolyomaVirus (MCPyV) in oral cavity lesions in Iranian patients. One hundred and fourteen oral cavity samples, including 33 oral squamous cell carcinoma, 28 oral lichen planus, 16 oral epithelial dysplasia and 37 oral irritation fibromas were analyzed for the HPV, EBV and MCPyV infection by quantitative real-time PCR. According to histological features 32.5% and 28.9% of cases were oral irritation fibroma and oral squamous cell carcinoma, respectively. Infection with at least two viruses was detected in 21.1% of patients. In this group, co-infection with HPV/EBV was identified in 37.5% of cases, HPV/MCPyV in 29.2%, EBV/MCPyV in 12.5%, and HPV/EBV/MCPyV in 20.8%. There was no statistically significant difference between multiple infections and anatomical locations of cancer. The prevalence of triple viral infection (HPV/EBV/MCPyV) in well differentiated tumors was higher than EBV or MCPyV single infection. This study revealed that co-infection of HPV, EBV and MCPyV can be detected in both malignant and non-malignant oral cavity tissues, and co-infection with all three viruses in well differentiated tumors can be shown as a synergistic hypothesis of the pathogenic role of these viruses in oral malignant transformation.

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伊朗口腔癌和恶性前病变中人类乳头瘤病毒、爱泼斯坦-巴氏病毒和梅克尔细胞多瘤病毒合并感染的流行率
人类乳头瘤病毒(HPV)被认为是口腔癌和恶性前病变的最重要风险因素;然而,与其他致癌病毒同时感染作为共同因素的病因学关联尚未得到明确证实。本研究旨在确定伊朗患者口腔病变中人类乳头瘤病毒(HPV)、爱泼斯坦-巴氏病毒(EBV)和梅克尔细胞多瘤病毒(MCPyV)的合并感染率。通过实时定量 PCR 分析了 114 份口腔样本,包括 33 份口腔鳞状细胞癌样本、28 份口腔扁平苔藓样本、16 份口腔上皮发育不良样本和 37 份口腔刺激性纤维瘤样本,以确定是否感染了 HPV、EBV 和 MCPyV。根据组织学特征,分别有 32.5% 和 28.9% 的病例为口腔刺激性纤维瘤和口腔鳞状细胞癌。21.1%的患者至少感染了两种病毒。其中,37.5%的病例同时感染了HPV/EBV,29.2%的病例同时感染了HPV/MCPyV,12.5%的病例同时感染了EBV/MCPyV,20.8%的病例同时感染了HPV/EBV/MCPyV。多重感染与癌症的解剖位置之间没有明显的统计学差异。在分化良好的肿瘤中,三重病毒感染(HPV/EBV/MCPyV)的发生率高于 EBV 或 MCPyV 单一感染。该研究表明,在恶性和非恶性口腔组织中均可检测到HPV、EBV和MCPyV的共感染,分化良好的肿瘤中三种病毒的共感染可作为这些病毒在口腔恶性转化中致病作用的协同假说。
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期刊介绍: The International Journal of Molecular and Cellular Medicine (IJMCM) is a peer-reviewed, quarterly publication of Cellular and Molecular Biology Research Center (CMBRC), Babol University of Medical Sciences, Babol, Iran. The journal covers all cellular & molecular biology and medicine disciplines such as the genetic basis of disease, biomarker discovery in diagnosis and treatment, genomics and proteomics, bioinformatics, computer applications in human biology, stem cells and tissue engineering, medical biotechnology, nanomedicine, cellular processes related to growth, death and survival, clinical biochemistry, molecular & cellular immunology, molecular and cellular aspects of infectious disease and cancer research. IJMCM is a free access journal. All open access articles published in IJMCM are distributed under the terms of the Creative Commons Attribution CC BY. The journal doesn''t have any submission and article processing charges (APCs).
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