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Detection and genotyping of CMV and HPV in tumors and fallopian tubes from epithelial ovarian cancer patients
Viral and bacterial infections are detected in epithelial ovarian cancer (EOC) tissues. Since the fallopian tubes are often affected by pelvic inflammatory disease (PID) and the majority of serous EOCs appear to originate from dysplastic lesions in the distal tube, it is relevant to consider the pot...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6934444/ https://www.ncbi.nlm.nih.gov/pubmed/31882737 http://dx.doi.org/10.1038/s41598-019-56448-1 |
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author | Paradowska, Edyta Jabłońska, Agnieszka Studzińska, Mirosława Wilczyński, Miłosz Wilczyński, Jacek R. |
author_facet | Paradowska, Edyta Jabłońska, Agnieszka Studzińska, Mirosława Wilczyński, Miłosz Wilczyński, Jacek R. |
author_sort | Paradowska, Edyta |
collection | PubMed |
description | Viral and bacterial infections are detected in epithelial ovarian cancer (EOC) tissues. Since the fallopian tubes are often affected by pelvic inflammatory disease (PID) and the majority of serous EOCs appear to originate from dysplastic lesions in the distal tube, it is relevant to consider the potential role that infectious agents may play in ovarian carcinogenesis. We sought to analyze the prevalence of human papillomavirus (HPV) and cytomegalovirus (CMV) in EOC tissue and fallopian tube specimens obtained at tumor resection. Ovarian cancer and fallopian tube tissue samples obtained from patients with EOC were analyzed by both qualitative and quantitative PCR to detect and quantify viral DNA. The presence of CMV and HPV DNA was detected in 70% and 74% cancerous ovarian tissues, respectively, and was significantly higher in EOC than in benign tumor cases (P ≤ 0.01). CMV or HPV infection was observed also in the fallopian tube samples. Infection with HPV16 was determined in 70% of EOC cases. Almost two thirds of EOC patients demonstrated coinfection with CMV and HPV in the pathological samples. The results revealed that the presence of CMV and HPV in EOC samples is common. CMV and HPV infections can be potential risks for EOC development. |
format | Online Article Text |
id | pubmed-6934444 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69344442019-12-29 Detection and genotyping of CMV and HPV in tumors and fallopian tubes from epithelial ovarian cancer patients Paradowska, Edyta Jabłońska, Agnieszka Studzińska, Mirosława Wilczyński, Miłosz Wilczyński, Jacek R. Sci Rep Article Viral and bacterial infections are detected in epithelial ovarian cancer (EOC) tissues. Since the fallopian tubes are often affected by pelvic inflammatory disease (PID) and the majority of serous EOCs appear to originate from dysplastic lesions in the distal tube, it is relevant to consider the potential role that infectious agents may play in ovarian carcinogenesis. We sought to analyze the prevalence of human papillomavirus (HPV) and cytomegalovirus (CMV) in EOC tissue and fallopian tube specimens obtained at tumor resection. Ovarian cancer and fallopian tube tissue samples obtained from patients with EOC were analyzed by both qualitative and quantitative PCR to detect and quantify viral DNA. The presence of CMV and HPV DNA was detected in 70% and 74% cancerous ovarian tissues, respectively, and was significantly higher in EOC than in benign tumor cases (P ≤ 0.01). CMV or HPV infection was observed also in the fallopian tube samples. Infection with HPV16 was determined in 70% of EOC cases. Almost two thirds of EOC patients demonstrated coinfection with CMV and HPV in the pathological samples. The results revealed that the presence of CMV and HPV in EOC samples is common. CMV and HPV infections can be potential risks for EOC development. Nature Publishing Group UK 2019-12-27 /pmc/articles/PMC6934444/ /pubmed/31882737 http://dx.doi.org/10.1038/s41598-019-56448-1 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Paradowska, Edyta Jabłońska, Agnieszka Studzińska, Mirosława Wilczyński, Miłosz Wilczyński, Jacek R. Detection and genotyping of CMV and HPV in tumors and fallopian tubes from epithelial ovarian cancer patients |
title | Detection and genotyping of CMV and HPV in tumors and fallopian tubes from epithelial ovarian cancer patients |
title_full | Detection and genotyping of CMV and HPV in tumors and fallopian tubes from epithelial ovarian cancer patients |
title_fullStr | Detection and genotyping of CMV and HPV in tumors and fallopian tubes from epithelial ovarian cancer patients |
title_full_unstemmed | Detection and genotyping of CMV and HPV in tumors and fallopian tubes from epithelial ovarian cancer patients |
title_short | Detection and genotyping of CMV and HPV in tumors and fallopian tubes from epithelial ovarian cancer patients |
title_sort | detection and genotyping of cmv and hpv in tumors and fallopian tubes from epithelial ovarian cancer patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6934444/ https://www.ncbi.nlm.nih.gov/pubmed/31882737 http://dx.doi.org/10.1038/s41598-019-56448-1 |
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