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Coinfection with Epstein-Barr Virus (EBV), Human Papilloma Virus (HPV) and Polyoma BK Virus (BKPyV) in Laryngeal, Oropharyngeal and Oral Cavity Cancer
Most research providing evidence for the role of oncogenic viruses in head and neck squamous cell carcinoma (SCC) development is focused on one type of virus without analyzing possible interactions between two or more types of viruses. The aim of this study was to analyse the prevalence of co-infect...
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Published in: | International journal of molecular sciences 2017-12, Vol.18 (12), p.2752 |
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description | Most research providing evidence for the role of oncogenic viruses in head and neck squamous cell carcinoma (SCC) development is focused on one type of virus without analyzing possible interactions between two or more types of viruses. The aim of this study was to analyse the prevalence of co-infection with human papillomavirus (HPV), Epstein-Barr virus (EBV) and polyoma BK virus (BKPyV) in oral, oropharyngeal and laryngeal squamous cell carcinomas in Polish patients. The correlations between viral infection, SCC, demographic parameters, evidence of metastases and grading were also investigated. Fresh-frozen tumour tissue samples were collected from 146 patients with laryngeal, oropharyngeal and oral cancer. After DNA extraction, the DNA of the studied viruses was detected using polymerase chain rection (PCR) assay. Males (87.7%) with a history of smoking (70.6%) and alcohol abuse (59.6%) prevailed in the studied group. Histological type G2 was recognized in 64.4% cases. The patients were most frequently diagnosed with T2 stage (36.3%) and with N1 stage (45.8%). Infection with at least two viruses was detected in 56.2% of patients. In this group, co-infection with HPV/EBV was identified in 34.1% of cases, EBV/BKV in 23.2%, HPV/BKV in 22.0%, and HPV/EBV/BKV in 20.7%. No difference of multiple infection in different locations of cancer was observed. The prevalence of poorly differentiated tumours (G3) was more frequent in co-infection with all three viruses than EBV or BKV alone. A significant correlation was observed between tumour dimensions (T) and lymph-node involvement (N) in co-infected patients compared to single infection. Further studies are necessary to clarify whether co-infection plays an important role in the initiation and/or progression of oncogenic transformation of oral, oropharyngeal and laryngeal epithelial cells. |
doi_str_mv | 10.3390/ijms18122752 |
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The aim of this study was to analyse the prevalence of co-infection with human papillomavirus (HPV), Epstein-Barr virus (EBV) and polyoma BK virus (BKPyV) in oral, oropharyngeal and laryngeal squamous cell carcinomas in Polish patients. The correlations between viral infection, SCC, demographic parameters, evidence of metastases and grading were also investigated. Fresh-frozen tumour tissue samples were collected from 146 patients with laryngeal, oropharyngeal and oral cancer. After DNA extraction, the DNA of the studied viruses was detected using polymerase chain rection (PCR) assay. Males (87.7%) with a history of smoking (70.6%) and alcohol abuse (59.6%) prevailed in the studied group. Histological type G2 was recognized in 64.4% cases. The patients were most frequently diagnosed with T2 stage (36.3%) and with N1 stage (45.8%). Infection with at least two viruses was detected in 56.2% of patients. In this group, co-infection with HPV/EBV was identified in 34.1% of cases, EBV/BKV in 23.2%, HPV/BKV in 22.0%, and HPV/EBV/BKV in 20.7%. No difference of multiple infection in different locations of cancer was observed. The prevalence of poorly differentiated tumours (G3) was more frequent in co-infection with all three viruses than EBV or BKV alone. A significant correlation was observed between tumour dimensions (T) and lymph-node involvement (N) in co-infected patients compared to single infection. Further studies are necessary to clarify whether co-infection plays an important role in the initiation and/or progression of oncogenic transformation of oral, oropharyngeal and laryngeal epithelial cells.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms18122752</identifier><identifier>PMID: 29257122</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Abuse ; Aged ; Alcohol abuse ; BK virus (BKV) ; Cancer ; Carcinoma, Squamous Cell - epidemiology ; co-infection ; Coinfection ; Demographics ; Deoxyribonucleic acid ; DNA ; DNA viruses ; Drug abuse ; Epithelial cells ; Epstein-Barr virus ; Epstein-Barr Virus Infections - epidemiology ; Epstein–Barr virus (EBV) ; Female ; Head & neck cancer ; Human papillomavirus ; human papillomavirus (HPV) ; Humans ; Infections ; laryngeal cancer ; Laryngeal carcinoma ; Lymph nodes ; Male ; Metastases ; Middle Aged ; Mouth Neoplasms - epidemiology ; Oral cancer ; Oral cavity ; oropharyngeal cancer ; Otorhinolaryngologic Neoplasms - epidemiology ; Papillomavirus Infections - epidemiology ; Patients ; Polyomavirus Infections - epidemiology ; Prevalence ; Smoking ; Squamous cell carcinoma ; squamous cell carcinoma (SCC) ; Tumor Virus Infections - epidemiology ; Tumors ; Viral infections ; Viruses</subject><ispartof>International journal of molecular sciences, 2017-12, Vol.18 (12), p.2752</ispartof><rights>Copyright MDPI AG 2017</rights><rights>2017 by the authors. 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c478t-28453a50d5810e3e979a1b9f0c04998017891768c5a2aa7c7439ee28d66834e83</citedby><cites>FETCH-LOGICAL-c478t-28453a50d5810e3e979a1b9f0c04998017891768c5a2aa7c7439ee28d66834e83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1988672821/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1988672821?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,74998</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29257122$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Drop, Bartłomiej</creatorcontrib><creatorcontrib>Strycharz-Dudziak, Małgorzata</creatorcontrib><creatorcontrib>Kliszczewska, Ewa</creatorcontrib><creatorcontrib>Polz-Dacewicz, Małgorzata</creatorcontrib><title>Coinfection with Epstein-Barr Virus (EBV), Human Papilloma Virus (HPV) and Polyoma BK Virus (BKPyV) in Laryngeal, Oropharyngeal and Oral Cavity Cancer</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>Most research providing evidence for the role of oncogenic viruses in head and neck squamous cell carcinoma (SCC) development is focused on one type of virus without analyzing possible interactions between two or more types of viruses. The aim of this study was to analyse the prevalence of co-infection with human papillomavirus (HPV), Epstein-Barr virus (EBV) and polyoma BK virus (BKPyV) in oral, oropharyngeal and laryngeal squamous cell carcinomas in Polish patients. The correlations between viral infection, SCC, demographic parameters, evidence of metastases and grading were also investigated. Fresh-frozen tumour tissue samples were collected from 146 patients with laryngeal, oropharyngeal and oral cancer. After DNA extraction, the DNA of the studied viruses was detected using polymerase chain rection (PCR) assay. Males (87.7%) with a history of smoking (70.6%) and alcohol abuse (59.6%) prevailed in the studied group. Histological type G2 was recognized in 64.4% cases. The patients were most frequently diagnosed with T2 stage (36.3%) and with N1 stage (45.8%). Infection with at least two viruses was detected in 56.2% of patients. In this group, co-infection with HPV/EBV was identified in 34.1% of cases, EBV/BKV in 23.2%, HPV/BKV in 22.0%, and HPV/EBV/BKV in 20.7%. No difference of multiple infection in different locations of cancer was observed. The prevalence of poorly differentiated tumours (G3) was more frequent in co-infection with all three viruses than EBV or BKV alone. A significant correlation was observed between tumour dimensions (T) and lymph-node involvement (N) in co-infected patients compared to single infection. Further studies are necessary to clarify whether co-infection plays an important role in the initiation and/or progression of oncogenic transformation of oral, oropharyngeal and laryngeal epithelial cells.</description><subject>Abuse</subject><subject>Aged</subject><subject>Alcohol abuse</subject><subject>BK virus (BKV)</subject><subject>Cancer</subject><subject>Carcinoma, Squamous Cell - epidemiology</subject><subject>co-infection</subject><subject>Coinfection</subject><subject>Demographics</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA viruses</subject><subject>Drug abuse</subject><subject>Epithelial cells</subject><subject>Epstein-Barr virus</subject><subject>Epstein-Barr Virus Infections - epidemiology</subject><subject>Epstein–Barr virus (EBV)</subject><subject>Female</subject><subject>Head & neck cancer</subject><subject>Human papillomavirus</subject><subject>human papillomavirus (HPV)</subject><subject>Humans</subject><subject>Infections</subject><subject>laryngeal cancer</subject><subject>Laryngeal carcinoma</subject><subject>Lymph nodes</subject><subject>Male</subject><subject>Metastases</subject><subject>Middle Aged</subject><subject>Mouth Neoplasms - epidemiology</subject><subject>Oral cancer</subject><subject>Oral cavity</subject><subject>oropharyngeal cancer</subject><subject>Otorhinolaryngologic Neoplasms - epidemiology</subject><subject>Papillomavirus Infections - epidemiology</subject><subject>Patients</subject><subject>Polyomavirus Infections - epidemiology</subject><subject>Prevalence</subject><subject>Smoking</subject><subject>Squamous cell carcinoma</subject><subject>squamous cell carcinoma (SCC)</subject><subject>Tumor Virus Infections - epidemiology</subject><subject>Tumors</subject><subject>Viral infections</subject><subject>Viruses</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdUl1r2zAUNWNj7bK97XkY9tJCvOnDsqSXwRKypTSQPGx5FbIsJwq25Ep2R_5If2-VpinpQHA_zrlH915uknyG4BvGHHw3uzZABhGiBL1JLmGOUAZAQd-e-RfJhxB2ACCMCH-fXCCOCI0ll8nD1Blba9UbZ9N_pt-msy702thsIr1P18YPIb2aTdbX43Q-tNKmK9mZpnGtPIHz1fo6lbZKV67ZH_KT2xM0uV3tI2hsupB-bzdaNuN06V23PYVPhUsfnam8N_0-Gqu0_5i8q2UT9KdnO0r-_pr9mc6zxfL3zfTnIlM5ZX2GWE6wJKAiDAKNNadcwpLXQIGccwYgZRzSgikikZRU0RxzrRGrioLhXDM8Sm6OupWTO9F508bGhJNGPCWc3wjpe6MaLRCO-5OQ8KKs8zJn8ZscA6QY5WXJCY1aP45a3VC2ulLa9nGuV6KvEWu2YuPuBaEE4vhGydWzgHd3gw69aE1Qummk1W4IAnLKKAK8QJH69T_qzg3exlVFFmMFRQwdBMdHlvIuBK_rl2YgEIfjEefHE-lfzgd4IZ-uBT8Clb69Kw</recordid><startdate>20171219</startdate><enddate>20171219</enddate><creator>Drop, Bartłomiej</creator><creator>Strycharz-Dudziak, Małgorzata</creator><creator>Kliszczewska, Ewa</creator><creator>Polz-Dacewicz, Małgorzata</creator><general>MDPI AG</general><general>MDPI</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20171219</creationdate><title>Coinfection with Epstein-Barr Virus (EBV), Human Papilloma Virus (HPV) and Polyoma BK Virus (BKPyV) in Laryngeal, Oropharyngeal and Oral Cavity Cancer</title><author>Drop, Bartłomiej ; Strycharz-Dudziak, Małgorzata ; Kliszczewska, Ewa ; Polz-Dacewicz, Małgorzata</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c478t-28453a50d5810e3e979a1b9f0c04998017891768c5a2aa7c7439ee28d66834e83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Abuse</topic><topic>Aged</topic><topic>Alcohol abuse</topic><topic>BK virus (BKV)</topic><topic>Cancer</topic><topic>Carcinoma, Squamous Cell - epidemiology</topic><topic>co-infection</topic><topic>Coinfection</topic><topic>Demographics</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA viruses</topic><topic>Drug abuse</topic><topic>Epithelial cells</topic><topic>Epstein-Barr virus</topic><topic>Epstein-Barr Virus Infections - epidemiology</topic><topic>Epstein–Barr virus (EBV)</topic><topic>Female</topic><topic>Head & neck cancer</topic><topic>Human papillomavirus</topic><topic>human papillomavirus (HPV)</topic><topic>Humans</topic><topic>Infections</topic><topic>laryngeal cancer</topic><topic>Laryngeal carcinoma</topic><topic>Lymph nodes</topic><topic>Male</topic><topic>Metastases</topic><topic>Middle Aged</topic><topic>Mouth Neoplasms - epidemiology</topic><topic>Oral cancer</topic><topic>Oral cavity</topic><topic>oropharyngeal cancer</topic><topic>Otorhinolaryngologic Neoplasms - epidemiology</topic><topic>Papillomavirus Infections - epidemiology</topic><topic>Patients</topic><topic>Polyomavirus Infections - epidemiology</topic><topic>Prevalence</topic><topic>Smoking</topic><topic>Squamous cell carcinoma</topic><topic>squamous cell carcinoma (SCC)</topic><topic>Tumor Virus Infections - epidemiology</topic><topic>Tumors</topic><topic>Viral infections</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Drop, Bartłomiej</creatorcontrib><creatorcontrib>Strycharz-Dudziak, Małgorzata</creatorcontrib><creatorcontrib>Kliszczewska, Ewa</creatorcontrib><creatorcontrib>Polz-Dacewicz, Małgorzata</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection (Proquest)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Research Library (ProQuest)</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Drop, Bartłomiej</au><au>Strycharz-Dudziak, Małgorzata</au><au>Kliszczewska, Ewa</au><au>Polz-Dacewicz, Małgorzata</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Coinfection with Epstein-Barr Virus (EBV), Human Papilloma Virus (HPV) and Polyoma BK Virus (BKPyV) in Laryngeal, Oropharyngeal and Oral Cavity Cancer</atitle><jtitle>International journal of molecular sciences</jtitle><addtitle>Int J Mol Sci</addtitle><date>2017-12-19</date><risdate>2017</risdate><volume>18</volume><issue>12</issue><spage>2752</spage><pages>2752-</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>Most research providing evidence for the role of oncogenic viruses in head and neck squamous cell carcinoma (SCC) development is focused on one type of virus without analyzing possible interactions between two or more types of viruses. The aim of this study was to analyse the prevalence of co-infection with human papillomavirus (HPV), Epstein-Barr virus (EBV) and polyoma BK virus (BKPyV) in oral, oropharyngeal and laryngeal squamous cell carcinomas in Polish patients. The correlations between viral infection, SCC, demographic parameters, evidence of metastases and grading were also investigated. Fresh-frozen tumour tissue samples were collected from 146 patients with laryngeal, oropharyngeal and oral cancer. After DNA extraction, the DNA of the studied viruses was detected using polymerase chain rection (PCR) assay. Males (87.7%) with a history of smoking (70.6%) and alcohol abuse (59.6%) prevailed in the studied group. Histological type G2 was recognized in 64.4% cases. The patients were most frequently diagnosed with T2 stage (36.3%) and with N1 stage (45.8%). Infection with at least two viruses was detected in 56.2% of patients. In this group, co-infection with HPV/EBV was identified in 34.1% of cases, EBV/BKV in 23.2%, HPV/BKV in 22.0%, and HPV/EBV/BKV in 20.7%. No difference of multiple infection in different locations of cancer was observed. The prevalence of poorly differentiated tumours (G3) was more frequent in co-infection with all three viruses than EBV or BKV alone. A significant correlation was observed between tumour dimensions (T) and lymph-node involvement (N) in co-infected patients compared to single infection. Further studies are necessary to clarify whether co-infection plays an important role in the initiation and/or progression of oncogenic transformation of oral, oropharyngeal and laryngeal epithelial cells.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>29257122</pmid><doi>10.3390/ijms18122752</doi><oa>free_for_read</oa></addata></record> |
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subjects | Abuse Aged Alcohol abuse BK virus (BKV) Cancer Carcinoma, Squamous Cell - epidemiology co-infection Coinfection Demographics Deoxyribonucleic acid DNA DNA viruses Drug abuse Epithelial cells Epstein-Barr virus Epstein-Barr Virus Infections - epidemiology Epstein–Barr virus (EBV) Female Head & neck cancer Human papillomavirus human papillomavirus (HPV) Humans Infections laryngeal cancer Laryngeal carcinoma Lymph nodes Male Metastases Middle Aged Mouth Neoplasms - epidemiology Oral cancer Oral cavity oropharyngeal cancer Otorhinolaryngologic Neoplasms - epidemiology Papillomavirus Infections - epidemiology Patients Polyomavirus Infections - epidemiology Prevalence Smoking Squamous cell carcinoma squamous cell carcinoma (SCC) Tumor Virus Infections - epidemiology Tumors Viral infections Viruses |
title | Coinfection with Epstein-Barr Virus (EBV), Human Papilloma Virus (HPV) and Polyoma BK Virus (BKPyV) in Laryngeal, Oropharyngeal and Oral Cavity Cancer |
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