Analysis of Sequence Variation and Risk Association of Human Papillomavirus 52 Variants Circulating in Korea

Human papillomavirus (HPV) 52 is a carcinogenic, high-risk genotype frequently detected in cervical cancer cases from East Asia, including Korea. Sequences of HPV52 detected in 91 cervical samples collected from women attending Seoul St. Mary's Hospital were analyzed. HPV52 genomic sequences we...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:PloS one 2016-12, Vol.11 (12), p.e0168178
Hauptverfasser: Choi, Youn Jin, Ki, Eun Young, Zhang, Chuqing, Ho, Wendy C S, Lee, Sung-Jong, Jeong, Min Jin, Chan, Paul K S, Park, Jong Sup
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue 12
container_start_page e0168178
container_title PloS one
container_volume 11
creator Choi, Youn Jin
Ki, Eun Young
Zhang, Chuqing
Ho, Wendy C S
Lee, Sung-Jong
Jeong, Min Jin
Chan, Paul K S
Park, Jong Sup
description Human papillomavirus (HPV) 52 is a carcinogenic, high-risk genotype frequently detected in cervical cancer cases from East Asia, including Korea. Sequences of HPV52 detected in 91 cervical samples collected from women attending Seoul St. Mary's Hospital were analyzed. HPV52 genomic sequences were obtained by polymerase chain reaction (PCR)-based sequencing and analyzed using Seq-Scape software, and phylogenetic trees were constructed using MEGA6 software. Of the 91 cervical samples, 40 were normal, 22 were low-grade lesions, 21 were high-grade lesions and 7 were squamous cell carcinomas. Four HPV52 variant lineages (A, B, C and D) were identified. Lineage B was the most frequently detected lineage, followed by lineage C. By analyzing the two most frequently detected lineages (B and C), we found that distinct variations existed in each lineage. We also found that a lineage B-specific mutation K93R (A379G) was associated with an increased risk of cervical neoplasia. To our knowledge, we are the first to reveal the predominance of the HPV52 lineages, B and C, in Korea. We also found these lineages harbored distinct genetic alterations that may affect oncogenicity. Our findings increase our understanding on the heterogeneity of HPV52 variants, and may be useful for the development of new diagnostic assays and therapeutic vaccines.
doi_str_mv 10.1371/journal.pone.0168178
format Article
fullrecord <record><control><sourceid>gale_plos_</sourceid><recordid>TN_cdi_plos_journals_1850130128</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A474010341</galeid><doaj_id>oai_doaj_org_article_a01c3fc446f0432280d664259c33124a</doaj_id><sourcerecordid>A474010341</sourcerecordid><originalsourceid>FETCH-LOGICAL-c791t-7ea9066fa3dc6f1ce403138ec935b034cb515b6c677aca545520b041f9ee7c8b3</originalsourceid><addsrcrecordid>eNqNk9Fu0zAUhiMEYmPwBggiISG4aLFjx05ukKoKWMWkoQ12a504Turi2J2dTOztcddsatAukC9sHX__b59jnyR5jdEcE44_bdzgLZj51lk1R5gVmBdPkmNckmzGMkSeHqyPkhchbBDKScHY8-Qo4yXnnOLjxCyix23QIXVNeqmuB2WlSq_Aa-i1synYOr3Q4Xe6CMHJMRjR06EDm_6ArTbGdXCj_RDSPNsrbR_SpfZyMJG3bapt-t15BS-TZw2YoF6N80ny6-uXn8vT2dn5t9VycTaTvMT9jCsoEWMNkFqyBktFEcGkULIkeYUIlVWO84pJxjlIyGmeZ6hCFDelUlwWFTlJ3u59t8YFMRYqCFzkCBOEsyISqz1RO9iIrdcd-FvhQIu7gPOtAN9raZQAhCVpJKWsQZRkWYFqxmiWl5IQnFGIXp_H04aqU7VUtvdgJqbTHavXonU3ImZRIMKiwYfRwLv4AKEXnQ5SGQNWueHu3iXlWU7KiL77B308u5FqISagbePiuXJnKhaUU4RjEXGk5o9QcdSq0zL-qkbH-ETwcSKITK_-9C0MIYjV5cX_s-dXU_b9AbtWYPp1cGbY_bUwBekelN6F4FXzUGSMxK4p7qshdk0hxqaIsjeHD_Qguu8C8hfovgXK</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1850130128</pqid></control><display><type>article</type><title>Analysis of Sequence Variation and Risk Association of Human Papillomavirus 52 Variants Circulating in Korea</title><source>MEDLINE</source><source>DOAJ Directory of Open Access Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Public Library of Science (PLoS) Journals Open Access</source><source>PubMed Central</source><source>Free Full-Text Journals in Chemistry</source><creator>Choi, Youn Jin ; Ki, Eun Young ; Zhang, Chuqing ; Ho, Wendy C S ; Lee, Sung-Jong ; Jeong, Min Jin ; Chan, Paul K S ; Park, Jong Sup</creator><contributor>Liu, Xuefeng</contributor><creatorcontrib>Choi, Youn Jin ; Ki, Eun Young ; Zhang, Chuqing ; Ho, Wendy C S ; Lee, Sung-Jong ; Jeong, Min Jin ; Chan, Paul K S ; Park, Jong Sup ; Liu, Xuefeng</creatorcontrib><description>Human papillomavirus (HPV) 52 is a carcinogenic, high-risk genotype frequently detected in cervical cancer cases from East Asia, including Korea. Sequences of HPV52 detected in 91 cervical samples collected from women attending Seoul St. Mary's Hospital were analyzed. HPV52 genomic sequences were obtained by polymerase chain reaction (PCR)-based sequencing and analyzed using Seq-Scape software, and phylogenetic trees were constructed using MEGA6 software. Of the 91 cervical samples, 40 were normal, 22 were low-grade lesions, 21 were high-grade lesions and 7 were squamous cell carcinomas. Four HPV52 variant lineages (A, B, C and D) were identified. Lineage B was the most frequently detected lineage, followed by lineage C. By analyzing the two most frequently detected lineages (B and C), we found that distinct variations existed in each lineage. We also found that a lineage B-specific mutation K93R (A379G) was associated with an increased risk of cervical neoplasia. To our knowledge, we are the first to reveal the predominance of the HPV52 lineages, B and C, in Korea. We also found these lineages harbored distinct genetic alterations that may affect oncogenicity. Our findings increase our understanding on the heterogeneity of HPV52 variants, and may be useful for the development of new diagnostic assays and therapeutic vaccines.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0168178</identifier><identifier>PMID: 27977741</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Biology and Life Sciences ; Carcinogens ; Carcinoma, Squamous Cell - pathology ; Carcinoma, Squamous Cell - virology ; Cell cycle ; Cellular biology ; Cervical cancer ; Cervix ; Computer programs ; Deoxyribonucleic acid ; Departments ; Diagnostic systems ; Distribution ; DNA ; DNA polymerase ; DNA, Viral ; Female ; Genetic aspects ; Genetic Variation ; Genotype &amp; phenotype ; Genotypes ; Gynecology ; Health aspects ; Health risks ; Human papillomavirus ; Humans ; Lesions ; Medicine ; Medicine and Health Sciences ; Mutation ; Obstetrics ; Papillomaviridae ; Papillomaviridae - genetics ; Papillomavirus ; Papillomavirus infections ; Papillomavirus Infections - pathology ; Papillomavirus Infections - virology ; Phylogeny ; Polymerase chain reaction ; Republic of Korea ; Research and Analysis Methods ; Risk ; Sequence Analysis, DNA ; Squamous cell carcinoma ; Thermal cycling ; Uterine Cervical Neoplasms - pathology ; Uterine Cervical Neoplasms - virology ; Vaccines</subject><ispartof>PloS one, 2016-12, Vol.11 (12), p.e0168178</ispartof><rights>COPYRIGHT 2016 Public Library of Science</rights><rights>2016 Choi et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2016 Choi et al 2016 Choi et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c791t-7ea9066fa3dc6f1ce403138ec935b034cb515b6c677aca545520b041f9ee7c8b3</citedby><cites>FETCH-LOGICAL-c791t-7ea9066fa3dc6f1ce403138ec935b034cb515b6c677aca545520b041f9ee7c8b3</cites><orcidid>0000-0003-4086-4885</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5158036/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5158036/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,729,782,786,866,887,2104,2930,23873,27931,27932,53798,53800</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27977741$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Liu, Xuefeng</contributor><creatorcontrib>Choi, Youn Jin</creatorcontrib><creatorcontrib>Ki, Eun Young</creatorcontrib><creatorcontrib>Zhang, Chuqing</creatorcontrib><creatorcontrib>Ho, Wendy C S</creatorcontrib><creatorcontrib>Lee, Sung-Jong</creatorcontrib><creatorcontrib>Jeong, Min Jin</creatorcontrib><creatorcontrib>Chan, Paul K S</creatorcontrib><creatorcontrib>Park, Jong Sup</creatorcontrib><title>Analysis of Sequence Variation and Risk Association of Human Papillomavirus 52 Variants Circulating in Korea</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Human papillomavirus (HPV) 52 is a carcinogenic, high-risk genotype frequently detected in cervical cancer cases from East Asia, including Korea. Sequences of HPV52 detected in 91 cervical samples collected from women attending Seoul St. Mary's Hospital were analyzed. HPV52 genomic sequences were obtained by polymerase chain reaction (PCR)-based sequencing and analyzed using Seq-Scape software, and phylogenetic trees were constructed using MEGA6 software. Of the 91 cervical samples, 40 were normal, 22 were low-grade lesions, 21 were high-grade lesions and 7 were squamous cell carcinomas. Four HPV52 variant lineages (A, B, C and D) were identified. Lineage B was the most frequently detected lineage, followed by lineage C. By analyzing the two most frequently detected lineages (B and C), we found that distinct variations existed in each lineage. We also found that a lineage B-specific mutation K93R (A379G) was associated with an increased risk of cervical neoplasia. To our knowledge, we are the first to reveal the predominance of the HPV52 lineages, B and C, in Korea. We also found these lineages harbored distinct genetic alterations that may affect oncogenicity. Our findings increase our understanding on the heterogeneity of HPV52 variants, and may be useful for the development of new diagnostic assays and therapeutic vaccines.</description><subject>Biology and Life Sciences</subject><subject>Carcinogens</subject><subject>Carcinoma, Squamous Cell - pathology</subject><subject>Carcinoma, Squamous Cell - virology</subject><subject>Cell cycle</subject><subject>Cellular biology</subject><subject>Cervical cancer</subject><subject>Cervix</subject><subject>Computer programs</subject><subject>Deoxyribonucleic acid</subject><subject>Departments</subject><subject>Diagnostic systems</subject><subject>Distribution</subject><subject>DNA</subject><subject>DNA polymerase</subject><subject>DNA, Viral</subject><subject>Female</subject><subject>Genetic aspects</subject><subject>Genetic Variation</subject><subject>Genotype &amp; phenotype</subject><subject>Genotypes</subject><subject>Gynecology</subject><subject>Health aspects</subject><subject>Health risks</subject><subject>Human papillomavirus</subject><subject>Humans</subject><subject>Lesions</subject><subject>Medicine</subject><subject>Medicine and Health Sciences</subject><subject>Mutation</subject><subject>Obstetrics</subject><subject>Papillomaviridae</subject><subject>Papillomaviridae - genetics</subject><subject>Papillomavirus</subject><subject>Papillomavirus infections</subject><subject>Papillomavirus Infections - pathology</subject><subject>Papillomavirus Infections - virology</subject><subject>Phylogeny</subject><subject>Polymerase chain reaction</subject><subject>Republic of Korea</subject><subject>Research and Analysis Methods</subject><subject>Risk</subject><subject>Sequence Analysis, DNA</subject><subject>Squamous cell carcinoma</subject><subject>Thermal cycling</subject><subject>Uterine Cervical Neoplasms - pathology</subject><subject>Uterine Cervical Neoplasms - virology</subject><subject>Vaccines</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNqNk9Fu0zAUhiMEYmPwBggiISG4aLFjx05ukKoKWMWkoQ12a504Turi2J2dTOztcddsatAukC9sHX__b59jnyR5jdEcE44_bdzgLZj51lk1R5gVmBdPkmNckmzGMkSeHqyPkhchbBDKScHY8-Qo4yXnnOLjxCyix23QIXVNeqmuB2WlSq_Aa-i1synYOr3Q4Xe6CMHJMRjR06EDm_6ArTbGdXCj_RDSPNsrbR_SpfZyMJG3bapt-t15BS-TZw2YoF6N80ny6-uXn8vT2dn5t9VycTaTvMT9jCsoEWMNkFqyBktFEcGkULIkeYUIlVWO84pJxjlIyGmeZ6hCFDelUlwWFTlJ3u59t8YFMRYqCFzkCBOEsyISqz1RO9iIrdcd-FvhQIu7gPOtAN9raZQAhCVpJKWsQZRkWYFqxmiWl5IQnFGIXp_H04aqU7VUtvdgJqbTHavXonU3ImZRIMKiwYfRwLv4AKEXnQ5SGQNWueHu3iXlWU7KiL77B308u5FqISagbePiuXJnKhaUU4RjEXGk5o9QcdSq0zL-qkbH-ETwcSKITK_-9C0MIYjV5cX_s-dXU_b9AbtWYPp1cGbY_bUwBekelN6F4FXzUGSMxK4p7qshdk0hxqaIsjeHD_Qguu8C8hfovgXK</recordid><startdate>20161215</startdate><enddate>20161215</enddate><creator>Choi, Youn Jin</creator><creator>Ki, Eun Young</creator><creator>Zhang, Chuqing</creator><creator>Ho, Wendy C S</creator><creator>Lee, Sung-Jong</creator><creator>Jeong, Min Jin</creator><creator>Chan, Paul K S</creator><creator>Park, Jong Sup</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-4086-4885</orcidid></search><sort><creationdate>20161215</creationdate><title>Analysis of Sequence Variation and Risk Association of Human Papillomavirus 52 Variants Circulating in Korea</title><author>Choi, Youn Jin ; Ki, Eun Young ; Zhang, Chuqing ; Ho, Wendy C S ; Lee, Sung-Jong ; Jeong, Min Jin ; Chan, Paul K S ; Park, Jong Sup</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c791t-7ea9066fa3dc6f1ce403138ec935b034cb515b6c677aca545520b041f9ee7c8b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Biology and Life Sciences</topic><topic>Carcinogens</topic><topic>Carcinoma, Squamous Cell - pathology</topic><topic>Carcinoma, Squamous Cell - virology</topic><topic>Cell cycle</topic><topic>Cellular biology</topic><topic>Cervical cancer</topic><topic>Cervix</topic><topic>Computer programs</topic><topic>Deoxyribonucleic acid</topic><topic>Departments</topic><topic>Diagnostic systems</topic><topic>Distribution</topic><topic>DNA</topic><topic>DNA polymerase</topic><topic>DNA, Viral</topic><topic>Female</topic><topic>Genetic aspects</topic><topic>Genetic Variation</topic><topic>Genotype &amp; phenotype</topic><topic>Genotypes</topic><topic>Gynecology</topic><topic>Health aspects</topic><topic>Health risks</topic><topic>Human papillomavirus</topic><topic>Humans</topic><topic>Lesions</topic><topic>Medicine</topic><topic>Medicine and Health Sciences</topic><topic>Mutation</topic><topic>Obstetrics</topic><topic>Papillomaviridae</topic><topic>Papillomaviridae - genetics</topic><topic>Papillomavirus</topic><topic>Papillomavirus infections</topic><topic>Papillomavirus Infections - pathology</topic><topic>Papillomavirus Infections - virology</topic><topic>Phylogeny</topic><topic>Polymerase chain reaction</topic><topic>Republic of Korea</topic><topic>Research and Analysis Methods</topic><topic>Risk</topic><topic>Sequence Analysis, DNA</topic><topic>Squamous cell carcinoma</topic><topic>Thermal cycling</topic><topic>Uterine Cervical Neoplasms - pathology</topic><topic>Uterine Cervical Neoplasms - virology</topic><topic>Vaccines</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Choi, Youn Jin</creatorcontrib><creatorcontrib>Ki, Eun Young</creatorcontrib><creatorcontrib>Zhang, Chuqing</creatorcontrib><creatorcontrib>Ho, Wendy C S</creatorcontrib><creatorcontrib>Lee, Sung-Jong</creatorcontrib><creatorcontrib>Jeong, Min Jin</creatorcontrib><creatorcontrib>Chan, Paul K S</creatorcontrib><creatorcontrib>Park, Jong Sup</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing &amp; Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological &amp; Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science &amp; Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies &amp; Aerospace Collection</collection><collection>Agricultural &amp; Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Meteorological &amp; Geoastrophysical Abstracts - Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Advanced Technologies &amp; Aerospace Database</collection><collection>ProQuest Advanced Technologies &amp; Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials Science Collection</collection><collection>Access via ProQuest (Open Access)</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>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Choi, Youn Jin</au><au>Ki, Eun Young</au><au>Zhang, Chuqing</au><au>Ho, Wendy C S</au><au>Lee, Sung-Jong</au><au>Jeong, Min Jin</au><au>Chan, Paul K S</au><au>Park, Jong Sup</au><au>Liu, Xuefeng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Analysis of Sequence Variation and Risk Association of Human Papillomavirus 52 Variants Circulating in Korea</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2016-12-15</date><risdate>2016</risdate><volume>11</volume><issue>12</issue><spage>e0168178</spage><pages>e0168178-</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Human papillomavirus (HPV) 52 is a carcinogenic, high-risk genotype frequently detected in cervical cancer cases from East Asia, including Korea. Sequences of HPV52 detected in 91 cervical samples collected from women attending Seoul St. Mary's Hospital were analyzed. HPV52 genomic sequences were obtained by polymerase chain reaction (PCR)-based sequencing and analyzed using Seq-Scape software, and phylogenetic trees were constructed using MEGA6 software. Of the 91 cervical samples, 40 were normal, 22 were low-grade lesions, 21 were high-grade lesions and 7 were squamous cell carcinomas. Four HPV52 variant lineages (A, B, C and D) were identified. Lineage B was the most frequently detected lineage, followed by lineage C. By analyzing the two most frequently detected lineages (B and C), we found that distinct variations existed in each lineage. We also found that a lineage B-specific mutation K93R (A379G) was associated with an increased risk of cervical neoplasia. To our knowledge, we are the first to reveal the predominance of the HPV52 lineages, B and C, in Korea. We also found these lineages harbored distinct genetic alterations that may affect oncogenicity. Our findings increase our understanding on the heterogeneity of HPV52 variants, and may be useful for the development of new diagnostic assays and therapeutic vaccines.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>27977741</pmid><doi>10.1371/journal.pone.0168178</doi><tpages>e0168178</tpages><orcidid>https://orcid.org/0000-0003-4086-4885</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1932-6203
ispartof PloS one, 2016-12, Vol.11 (12), p.e0168178
issn 1932-6203
1932-6203
language eng
recordid cdi_plos_journals_1850130128
source MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Public Library of Science (PLoS) Journals Open Access; PubMed Central; Free Full-Text Journals in Chemistry
subjects Biology and Life Sciences
Carcinogens
Carcinoma, Squamous Cell - pathology
Carcinoma, Squamous Cell - virology
Cell cycle
Cellular biology
Cervical cancer
Cervix
Computer programs
Deoxyribonucleic acid
Departments
Diagnostic systems
Distribution
DNA
DNA polymerase
DNA, Viral
Female
Genetic aspects
Genetic Variation
Genotype & phenotype
Genotypes
Gynecology
Health aspects
Health risks
Human papillomavirus
Humans
Lesions
Medicine
Medicine and Health Sciences
Mutation
Obstetrics
Papillomaviridae
Papillomaviridae - genetics
Papillomavirus
Papillomavirus infections
Papillomavirus Infections - pathology
Papillomavirus Infections - virology
Phylogeny
Polymerase chain reaction
Republic of Korea
Research and Analysis Methods
Risk
Sequence Analysis, DNA
Squamous cell carcinoma
Thermal cycling
Uterine Cervical Neoplasms - pathology
Uterine Cervical Neoplasms - virology
Vaccines
title Analysis of Sequence Variation and Risk Association of Human Papillomavirus 52 Variants Circulating in Korea
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-04T07%3A33%3A22IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Analysis%20of%20Sequence%20Variation%20and%20Risk%20Association%20of%20Human%20Papillomavirus%2052%20Variants%20Circulating%20in%20Korea&rft.jtitle=PloS%20one&rft.au=Choi,%20Youn%20Jin&rft.date=2016-12-15&rft.volume=11&rft.issue=12&rft.spage=e0168178&rft.pages=e0168178-&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0168178&rft_dat=%3Cgale_plos_%3EA474010341%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1850130128&rft_id=info:pmid/27977741&rft_galeid=A474010341&rft_doaj_id=oai_doaj_org_article_a01c3fc446f0432280d664259c33124a&rfr_iscdi=true