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Unusually high incidence of polyomavirus JC infection in the higher grade of colorectal cancer tissues in Taiwan
Introduction The human JC polyomavirus (JCPyV) has been detected in colorectal cancer (CRC) tissues and is suggested to contribute to CRC tumorigenesis. The rearrangement of the JCPyV regulatory region is supposedly associated with CRC development. The progression of CRC involves the stepwise accumu...
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Published in: | European journal of medical research 2022-07, Vol.27 (1), p.1-127, Article 127 |
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description | Introduction The human JC polyomavirus (JCPyV) has been detected in colorectal cancer (CRC) tissues and is suggested to contribute to CRC tumorigenesis. The rearrangement of the JCPyV regulatory region is supposedly associated with CRC development. The progression of CRC involves the stepwise accumulation of mutations. The large tumor antigen (LT) of JCPyV can trigger uncontrolled cell cycle progression by targeting oncogenes, and tumor suppressor genes, and causing chromosome instability. Few studies have focused on the presence of JCPyV DNA in the higher grade of CRC tissues. Methods We collected 95 tissue blocks from samples of stages I, II, III, and IV CRC. Nested PCR targeting the regulatory region of the viral genome was performed to determine the presence of JCPyV DNA in the various stages of colorectal cancer tissues. Results The nested PCR results showed that the positive rate of JCPyV DNA increased with the progression of CRC stages. The archetypal-like, non-rearrangement genotype of JCPyV with subtle mutations was the major genotype found in CRC samples. Conclusions This finding in our study suggests that there may be an association between JCPyV and CRC progression. Keywords: JCPyV, Colorectal cancer, Nested PCR, Tumor progression, DNA virus |
doi_str_mv | 10.1186/s40001-022-00756-2 |
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The rearrangement of the JCPyV regulatory region is supposedly associated with CRC development. The progression of CRC involves the stepwise accumulation of mutations. The large tumor antigen (LT) of JCPyV can trigger uncontrolled cell cycle progression by targeting oncogenes, and tumor suppressor genes, and causing chromosome instability. Few studies have focused on the presence of JCPyV DNA in the higher grade of CRC tissues. Methods We collected 95 tissue blocks from samples of stages I, II, III, and IV CRC. Nested PCR targeting the regulatory region of the viral genome was performed to determine the presence of JCPyV DNA in the various stages of colorectal cancer tissues. Results The nested PCR results showed that the positive rate of JCPyV DNA increased with the progression of CRC stages. The archetypal-like, non-rearrangement genotype of JCPyV with subtle mutations was the major genotype found in CRC samples. Conclusions This finding in our study suggests that there may be an association between JCPyV and CRC progression. Keywords: JCPyV, Colorectal cancer, Nested PCR, Tumor progression, DNA virus</description><identifier>ISSN: 2047-783X</identifier><identifier>ISSN: 0949-2321</identifier><identifier>EISSN: 2047-783X</identifier><identifier>DOI: 10.1186/s40001-022-00756-2</identifier><identifier>PMID: 35859146</identifier><language>eng</language><publisher>London: BioMed Central Ltd</publisher><subject>Antigens ; Biobanks ; Colorectal cancer ; Development and progression ; DNA virus ; Genes ; Genetic testing ; Genomes ; Genomics ; Health aspects ; JCPyV ; Mutation ; Nested PCR ; Polymerase chain reaction ; Tumor progression ; Tumors</subject><ispartof>European journal of medical research, 2022-07, Vol.27 (1), p.1-127, Article 127</ispartof><rights>COPYRIGHT 2022 BioMed Central Ltd.</rights><rights>2022. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c571t-bbd01acbaeda87474382c4f576078e6a70a4aae14d462c4e08ec2367c456fdb13</citedby><cites>FETCH-LOGICAL-c571t-bbd01acbaeda87474382c4f576078e6a70a4aae14d462c4e08ec2367c456fdb13</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/PMC9301828/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2703685614?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids></links><search><creatorcontrib>Fang, Chuan-Yin</creatorcontrib><creatorcontrib>Chen, San-Yuan</creatorcontrib><creatorcontrib>Hsiao, Bo-Xiu</creatorcontrib><creatorcontrib>Huang, Hsin-Yi</creatorcontrib><creatorcontrib>Chen, Yi-Ju</creatorcontrib><creatorcontrib>Tung, Chun-Liang</creatorcontrib><creatorcontrib>Fang, Chiung-Yao</creatorcontrib><title>Unusually high incidence of polyomavirus JC infection in the higher grade of colorectal cancer tissues in Taiwan</title><title>European journal of medical research</title><description>Introduction The human JC polyomavirus (JCPyV) has been detected in colorectal cancer (CRC) tissues and is suggested to contribute to CRC tumorigenesis. The rearrangement of the JCPyV regulatory region is supposedly associated with CRC development. The progression of CRC involves the stepwise accumulation of mutations. The large tumor antigen (LT) of JCPyV can trigger uncontrolled cell cycle progression by targeting oncogenes, and tumor suppressor genes, and causing chromosome instability. Few studies have focused on the presence of JCPyV DNA in the higher grade of CRC tissues. Methods We collected 95 tissue blocks from samples of stages I, II, III, and IV CRC. Nested PCR targeting the regulatory region of the viral genome was performed to determine the presence of JCPyV DNA in the various stages of colorectal cancer tissues. Results The nested PCR results showed that the positive rate of JCPyV DNA increased with the progression of CRC stages. The archetypal-like, non-rearrangement genotype of JCPyV with subtle mutations was the major genotype found in CRC samples. Conclusions This finding in our study suggests that there may be an association between JCPyV and CRC progression. Keywords: JCPyV, Colorectal cancer, Nested PCR, Tumor progression, DNA virus</description><subject>Antigens</subject><subject>Biobanks</subject><subject>Colorectal cancer</subject><subject>Development and progression</subject><subject>DNA virus</subject><subject>Genes</subject><subject>Genetic testing</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Health aspects</subject><subject>JCPyV</subject><subject>Mutation</subject><subject>Nested PCR</subject><subject>Polymerase chain reaction</subject><subject>Tumor progression</subject><subject>Tumors</subject><issn>2047-783X</issn><issn>0949-2321</issn><issn>2047-783X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkk1rGzEQhpfS0oQ0f6CnhULpZVNJq5W0l0Iw_UgJ9JJAb2JWGtky8sqVdhP87yvboY1L0UFi5nlfSTNTVW8puaJUiY-ZE0JoQxhrCJGdaNiL6pwRLhup2p8vn53Pqsuc14UmggnZ96-rs7ZTXU-5OK-29-OcZwhhV6_8clX70XiLo8E6unobwy5u4MGnOdffFyXp0Ew-juVUTys8SDDVywT2IDAxxFQQCLWBYpLqyec8Y94L7sA_wvimeuUgZLx82i-q-y-f7xbfmtsfX28W17eN6SSdmmGwhIIZAC0oySVvFTPcdVIQqVCAJMABkHLLRUkgUWhYK6ThnXB2oO1FdXP0tRHWepv8BtJOR_D6EIhpqSFN3gTUTEnhHBedoMCltWpQTrjecu4kmo4Vr09Hr-08bNAaHKcE4cT0NDP6lV7GB923hCqmisGHJ4MUf5VyTHrjs8EQYMQ4Z81Ez2QnW7JH3_2DruOcxlIqzSRphSqv5H-pJZQPlL7Ecq_Zm-prSUkvJe9Foa7-Q5VlceNNHNH5Ej8RvH8mWCGEaZVjmPc9z6cgO4ImxZwTuj_FoETv51Mf51OX-dSH-dSs_Q1TvtYc</recordid><startdate>20220720</startdate><enddate>20220720</enddate><creator>Fang, Chuan-Yin</creator><creator>Chen, San-Yuan</creator><creator>Hsiao, Bo-Xiu</creator><creator>Huang, Hsin-Yi</creator><creator>Chen, Yi-Ju</creator><creator>Tung, Chun-Liang</creator><creator>Fang, Chiung-Yao</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</general><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>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20220720</creationdate><title>Unusually high incidence of polyomavirus JC infection in the higher grade of colorectal cancer tissues in Taiwan</title><author>Fang, Chuan-Yin ; Chen, San-Yuan ; Hsiao, Bo-Xiu ; Huang, Hsin-Yi ; Chen, Yi-Ju ; Tung, Chun-Liang ; Fang, Chiung-Yao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c571t-bbd01acbaeda87474382c4f576078e6a70a4aae14d462c4e08ec2367c456fdb13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Antigens</topic><topic>Biobanks</topic><topic>Colorectal cancer</topic><topic>Development and progression</topic><topic>DNA virus</topic><topic>Genes</topic><topic>Genetic testing</topic><topic>Genomes</topic><topic>Genomics</topic><topic>Health aspects</topic><topic>JCPyV</topic><topic>Mutation</topic><topic>Nested PCR</topic><topic>Polymerase chain reaction</topic><topic>Tumor progression</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fang, Chuan-Yin</creatorcontrib><creatorcontrib>Chen, San-Yuan</creatorcontrib><creatorcontrib>Hsiao, Bo-Xiu</creatorcontrib><creatorcontrib>Huang, Hsin-Yi</creatorcontrib><creatorcontrib>Chen, Yi-Ju</creatorcontrib><creatorcontrib>Tung, Chun-Liang</creatorcontrib><creatorcontrib>Fang, Chiung-Yao</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest - Health & Medical Complete保健、医学与药学数据库</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>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: 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>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>European journal of medical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fang, Chuan-Yin</au><au>Chen, San-Yuan</au><au>Hsiao, Bo-Xiu</au><au>Huang, Hsin-Yi</au><au>Chen, Yi-Ju</au><au>Tung, Chun-Liang</au><au>Fang, Chiung-Yao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Unusually high incidence of polyomavirus JC infection in the higher grade of colorectal cancer tissues in Taiwan</atitle><jtitle>European journal of medical research</jtitle><date>2022-07-20</date><risdate>2022</risdate><volume>27</volume><issue>1</issue><spage>1</spage><epage>127</epage><pages>1-127</pages><artnum>127</artnum><issn>2047-783X</issn><issn>0949-2321</issn><eissn>2047-783X</eissn><abstract>Introduction The human JC polyomavirus (JCPyV) has been detected in colorectal cancer (CRC) tissues and is suggested to contribute to CRC tumorigenesis. The rearrangement of the JCPyV regulatory region is supposedly associated with CRC development. The progression of CRC involves the stepwise accumulation of mutations. The large tumor antigen (LT) of JCPyV can trigger uncontrolled cell cycle progression by targeting oncogenes, and tumor suppressor genes, and causing chromosome instability. Few studies have focused on the presence of JCPyV DNA in the higher grade of CRC tissues. Methods We collected 95 tissue blocks from samples of stages I, II, III, and IV CRC. Nested PCR targeting the regulatory region of the viral genome was performed to determine the presence of JCPyV DNA in the various stages of colorectal cancer tissues. Results The nested PCR results showed that the positive rate of JCPyV DNA increased with the progression of CRC stages. The archetypal-like, non-rearrangement genotype of JCPyV with subtle mutations was the major genotype found in CRC samples. Conclusions This finding in our study suggests that there may be an association between JCPyV and CRC progression. Keywords: JCPyV, Colorectal cancer, Nested PCR, Tumor progression, DNA virus</abstract><cop>London</cop><pub>BioMed Central Ltd</pub><pmid>35859146</pmid><doi>10.1186/s40001-022-00756-2</doi><oa>free_for_read</oa></addata></record> |
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subjects | Antigens Biobanks Colorectal cancer Development and progression DNA virus Genes Genetic testing Genomes Genomics Health aspects JCPyV Mutation Nested PCR Polymerase chain reaction Tumor progression Tumors |
title | Unusually high incidence of polyomavirus JC infection in the higher grade of colorectal cancer tissues in Taiwan |
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