Oncogenic viruses associated with vulva cancer in HIV-1 patients in Botswana
Oncoviruses such as HPV, KSHV, and EBV have been reported in patients with HIV infection and AIDS. How oncovirus-associated cancers rise in AIDS patients has not been fully established. The purpose of our study was to identify the viral agents in vulvar cancer and to assess their contribution to pat...
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description | Oncoviruses such as HPV, KSHV, and EBV have been reported in patients with HIV infection and AIDS. How oncovirus-associated cancers rise in AIDS patients has not been fully established. The purpose of our study was to identify the viral agents in vulvar cancer and to assess their contribution to pathogenesis.
We retrospectively identified a total of 13 vulva tissue samples from HIV-1 positive and 9 vulvar samples from HIV-1 negative patients from the Botswana National Health Laboratory in Gaborone, Botswana, a Southern African country with a high incidence of HIV. We utilized PCR and IHC to identify HPV, EBV, KSHV, and JC virus in FFPE preserved tissue samples.
Using the GP5(+)/GP6(+) primer set we detected several HPV types in tissue samples. EBV was detected in all of the positive cases (100%) and in most of the negative cases (89%). KSHV was detected in 39% of the HIV-1 positive samples and in 11% of the negative samples, and no JC virus was detected in any of the samples. Using IHC we demonstrated that LANA was expressed in 61% of the positive samples and in 44% of the negative samples. The ubiquitous EBV was more consistently expressed in negative cases (100%) than in positive cases (69%). Interestingly, the HPV-16 E6 transcript was detected in 56% of the negative samples compared to 31% of the positive samples. However, the cell cycle protein P21 used as a surrogate marker for HPV was detected in 77% of the positive samples and in 44% of the negative samples, while VEGF signals were similar in both positive (92%) and negative samples (89%).
Our study, suggests that in Botswana, vulvar squamous cell carcinoma (VSCC) is associated with oncogenic viruses present in the niche but the contribution and progression may be regulated by HPV and other immunosuppressive infections that include HIV-1. |
doi_str_mv | 10.1186/1750-9378-9-28 |
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We retrospectively identified a total of 13 vulva tissue samples from HIV-1 positive and 9 vulvar samples from HIV-1 negative patients from the Botswana National Health Laboratory in Gaborone, Botswana, a Southern African country with a high incidence of HIV. We utilized PCR and IHC to identify HPV, EBV, KSHV, and JC virus in FFPE preserved tissue samples.
Using the GP5(+)/GP6(+) primer set we detected several HPV types in tissue samples. EBV was detected in all of the positive cases (100%) and in most of the negative cases (89%). KSHV was detected in 39% of the HIV-1 positive samples and in 11% of the negative samples, and no JC virus was detected in any of the samples. Using IHC we demonstrated that LANA was expressed in 61% of the positive samples and in 44% of the negative samples. The ubiquitous EBV was more consistently expressed in negative cases (100%) than in positive cases (69%). Interestingly, the HPV-16 E6 transcript was detected in 56% of the negative samples compared to 31% of the positive samples. However, the cell cycle protein P21 used as a surrogate marker for HPV was detected in 77% of the positive samples and in 44% of the negative samples, while VEGF signals were similar in both positive (92%) and negative samples (89%).
Our study, suggests that in Botswana, vulvar squamous cell carcinoma (VSCC) is associated with oncogenic viruses present in the niche but the contribution and progression may be regulated by HPV and other immunosuppressive infections that include HIV-1.</description><identifier>ISSN: 1750-9378</identifier><identifier>EISSN: 1750-9378</identifier><identifier>DOI: 10.1186/1750-9378-9-28</identifier><identifier>PMID: 25225572</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Acquired immune deficiency syndrome ; Age ; AIDS ; Cancer patients ; Cell cycle ; Complications and side effects ; Deoxyribonucleic acid ; Development and progression ; Diagnosis ; DNA ; Epstein-Barr virus ; Genital cancers ; Health aspects ; HIV ; HIV infection ; Hospitals ; Human immunodeficiency virus ; Human immunodeficiency virus 1 ; Human papillomavirus ; Infections ; JC virus ; Kaposi's sarcoma-associated herpesvirus ; Laboratories ; Mutation ; Pathogenesis ; Patient outcomes ; Patients ; Proteins ; Sample size ; Squamous cell carcinoma ; Studies ; Thermal cycling ; Viral infections ; Viruses ; Womens health</subject><ispartof>Infectious agents and cancer, 2014-08, Vol.9 (1), p.28-28, Article 28</ispartof><rights>COPYRIGHT 2014 BioMed Central Ltd.</rights><rights>2014 Simbiri et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.</rights><rights>Copyright © 2014 Simbiri et al.; licensee BioMed Central Ltd. 2014 Simbiri et al.; licensee BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c518t-d6cb154eca1a229be26a331157387926615943c654b9a3e52c2d53c7327a52fd3</citedby><cites>FETCH-LOGICAL-c518t-d6cb154eca1a229be26a331157387926615943c654b9a3e52c2d53c7327a52fd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4164322/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4164322/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25225572$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Simbiri, Kenneth O</creatorcontrib><creatorcontrib>Jha, Hem C</creatorcontrib><creatorcontrib>Kayembe, Mukendi K</creatorcontrib><creatorcontrib>Kovarik, Carrie</creatorcontrib><creatorcontrib>Robertson, Erle S</creatorcontrib><title>Oncogenic viruses associated with vulva cancer in HIV-1 patients in Botswana</title><title>Infectious agents and cancer</title><addtitle>Infect Agent Cancer</addtitle><description>Oncoviruses such as HPV, KSHV, and EBV have been reported in patients with HIV infection and AIDS. How oncovirus-associated cancers rise in AIDS patients has not been fully established. The purpose of our study was to identify the viral agents in vulvar cancer and to assess their contribution to pathogenesis.
We retrospectively identified a total of 13 vulva tissue samples from HIV-1 positive and 9 vulvar samples from HIV-1 negative patients from the Botswana National Health Laboratory in Gaborone, Botswana, a Southern African country with a high incidence of HIV. We utilized PCR and IHC to identify HPV, EBV, KSHV, and JC virus in FFPE preserved tissue samples.
Using the GP5(+)/GP6(+) primer set we detected several HPV types in tissue samples. EBV was detected in all of the positive cases (100%) and in most of the negative cases (89%). KSHV was detected in 39% of the HIV-1 positive samples and in 11% of the negative samples, and no JC virus was detected in any of the samples. Using IHC we demonstrated that LANA was expressed in 61% of the positive samples and in 44% of the negative samples. The ubiquitous EBV was more consistently expressed in negative cases (100%) than in positive cases (69%). Interestingly, the HPV-16 E6 transcript was detected in 56% of the negative samples compared to 31% of the positive samples. However, the cell cycle protein P21 used as a surrogate marker for HPV was detected in 77% of the positive samples and in 44% of the negative samples, while VEGF signals were similar in both positive (92%) and negative samples (89%).
Our study, suggests that in Botswana, vulvar squamous cell carcinoma (VSCC) is associated with oncogenic viruses present in the niche but the contribution and progression may be regulated by HPV and other immunosuppressive infections that include HIV-1.</description><subject>Acquired immune deficiency syndrome</subject><subject>Age</subject><subject>AIDS</subject><subject>Cancer patients</subject><subject>Cell cycle</subject><subject>Complications and side effects</subject><subject>Deoxyribonucleic acid</subject><subject>Development and progression</subject><subject>Diagnosis</subject><subject>DNA</subject><subject>Epstein-Barr virus</subject><subject>Genital cancers</subject><subject>Health aspects</subject><subject>HIV</subject><subject>HIV infection</subject><subject>Hospitals</subject><subject>Human immunodeficiency virus</subject><subject>Human immunodeficiency virus 1</subject><subject>Human papillomavirus</subject><subject>Infections</subject><subject>JC virus</subject><subject>Kaposi's sarcoma-associated herpesvirus</subject><subject>Laboratories</subject><subject>Mutation</subject><subject>Pathogenesis</subject><subject>Patient outcomes</subject><subject>Patients</subject><subject>Proteins</subject><subject>Sample size</subject><subject>Squamous cell carcinoma</subject><subject>Studies</subject><subject>Thermal cycling</subject><subject>Viral infections</subject><subject>Viruses</subject><subject>Womens health</subject><issn>1750-9378</issn><issn>1750-9378</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNqNkkFP3DAQha2qqFDg2mMVqRcugXgcO86lEkVtQVqJS9urNetMFqOsvbWTRf33OC0stOJQ-WDr-Zunp9Fj7B2vTjnX6ow3sipb0eiyLUG_Ygc74fWz9z57m9JtVdUatH7D9kECSNnAAVtcextW5J0tti5OiVKBKQXrcKSuuHPjTbGdhi0WFr2lWDhfXF79KHmxwdGRH9OsfApjukOPR2yvxyHR8cN9yL5_-fzt4rJcXH-9ujhflFZyPZadsksua7LIEaBdEigUgnPZCN20oBSXbS2skvWyRUESLHRS2EZAgxL6Thyyj398N9NyTZ3NOSIOZhPdGuMvE9CZv3-8uzGrsDU1V7UAyAYnDwYx_JwojWbtkqVhQE9hSoZLpbQAkWP8BzonVqLJ6Id_0NswRZ838ZsSoGqonqgVDmSc70OOaGdTcy7rSklQQmTq9AUqn47WzgZPvcv6SwM2hpQi9bt18MrMVTFzG8zcBtMa0Hng_fMl7vDHboh7sLO11g</recordid><startdate>20140824</startdate><enddate>20140824</enddate><creator>Simbiri, Kenneth O</creator><creator>Jha, Hem C</creator><creator>Kayembe, Mukendi K</creator><creator>Kovarik, Carrie</creator><creator>Robertson, Erle S</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TO</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</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>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20140824</creationdate><title>Oncogenic viruses associated with vulva cancer in HIV-1 patients in Botswana</title><author>Simbiri, Kenneth O ; Jha, Hem C ; Kayembe, Mukendi K ; Kovarik, Carrie ; Robertson, Erle S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c518t-d6cb154eca1a229be26a331157387926615943c654b9a3e52c2d53c7327a52fd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Acquired immune deficiency syndrome</topic><topic>Age</topic><topic>AIDS</topic><topic>Cancer patients</topic><topic>Cell cycle</topic><topic>Complications and side effects</topic><topic>Deoxyribonucleic acid</topic><topic>Development and progression</topic><topic>Diagnosis</topic><topic>DNA</topic><topic>Epstein-Barr virus</topic><topic>Genital cancers</topic><topic>Health aspects</topic><topic>HIV</topic><topic>HIV infection</topic><topic>Hospitals</topic><topic>Human immunodeficiency virus</topic><topic>Human immunodeficiency virus 1</topic><topic>Human papillomavirus</topic><topic>Infections</topic><topic>JC virus</topic><topic>Kaposi's sarcoma-associated herpesvirus</topic><topic>Laboratories</topic><topic>Mutation</topic><topic>Pathogenesis</topic><topic>Patient outcomes</topic><topic>Patients</topic><topic>Proteins</topic><topic>Sample size</topic><topic>Squamous cell carcinoma</topic><topic>Studies</topic><topic>Thermal cycling</topic><topic>Viral infections</topic><topic>Viruses</topic><topic>Womens health</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Simbiri, Kenneth O</creatorcontrib><creatorcontrib>Jha, Hem C</creatorcontrib><creatorcontrib>Kayembe, Mukendi K</creatorcontrib><creatorcontrib>Kovarik, Carrie</creatorcontrib><creatorcontrib>Robertson, Erle S</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content Database</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Infectious agents and cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Simbiri, Kenneth O</au><au>Jha, Hem C</au><au>Kayembe, Mukendi K</au><au>Kovarik, Carrie</au><au>Robertson, Erle S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Oncogenic viruses associated with vulva cancer in HIV-1 patients in Botswana</atitle><jtitle>Infectious agents and cancer</jtitle><addtitle>Infect Agent Cancer</addtitle><date>2014-08-24</date><risdate>2014</risdate><volume>9</volume><issue>1</issue><spage>28</spage><epage>28</epage><pages>28-28</pages><artnum>28</artnum><issn>1750-9378</issn><eissn>1750-9378</eissn><abstract>Oncoviruses such as HPV, KSHV, and EBV have been reported in patients with HIV infection and AIDS. How oncovirus-associated cancers rise in AIDS patients has not been fully established. The purpose of our study was to identify the viral agents in vulvar cancer and to assess their contribution to pathogenesis.
We retrospectively identified a total of 13 vulva tissue samples from HIV-1 positive and 9 vulvar samples from HIV-1 negative patients from the Botswana National Health Laboratory in Gaborone, Botswana, a Southern African country with a high incidence of HIV. We utilized PCR and IHC to identify HPV, EBV, KSHV, and JC virus in FFPE preserved tissue samples.
Using the GP5(+)/GP6(+) primer set we detected several HPV types in tissue samples. EBV was detected in all of the positive cases (100%) and in most of the negative cases (89%). KSHV was detected in 39% of the HIV-1 positive samples and in 11% of the negative samples, and no JC virus was detected in any of the samples. Using IHC we demonstrated that LANA was expressed in 61% of the positive samples and in 44% of the negative samples. The ubiquitous EBV was more consistently expressed in negative cases (100%) than in positive cases (69%). Interestingly, the HPV-16 E6 transcript was detected in 56% of the negative samples compared to 31% of the positive samples. However, the cell cycle protein P21 used as a surrogate marker for HPV was detected in 77% of the positive samples and in 44% of the negative samples, while VEGF signals were similar in both positive (92%) and negative samples (89%).
Our study, suggests that in Botswana, vulvar squamous cell carcinoma (VSCC) is associated with oncogenic viruses present in the niche but the contribution and progression may be regulated by HPV and other immunosuppressive infections that include HIV-1.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>25225572</pmid><doi>10.1186/1750-9378-9-28</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acquired immune deficiency syndrome Age AIDS Cancer patients Cell cycle Complications and side effects Deoxyribonucleic acid Development and progression Diagnosis DNA Epstein-Barr virus Genital cancers Health aspects HIV HIV infection Hospitals Human immunodeficiency virus Human immunodeficiency virus 1 Human papillomavirus Infections JC virus Kaposi's sarcoma-associated herpesvirus Laboratories Mutation Pathogenesis Patient outcomes Patients Proteins Sample size Squamous cell carcinoma Studies Thermal cycling Viral infections Viruses Womens health |
title | Oncogenic viruses associated with vulva cancer in HIV-1 patients in Botswana |
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