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The clinical significance of FAM19A4 methylation in high-risk HPV-positive cervical samples for the detection of cervical (pre)cancer in Chinese women
To explore the diagnostic value of FAM19A4 methylation in high-risk human papilloma virus (hrHPV)-positive cervical samples from Chinese women for estimating cervical cancer or its precancerous lesions. Cervical samples from 215 women infected with high-risk HPV were collected by smear testing. We p...
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Published in: | BMC cancer 2018-11, Vol.18 (1), p.1182-1182, Article 1182 |
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description | To explore the diagnostic value of FAM19A4 methylation in high-risk human papilloma virus (hrHPV)-positive cervical samples from Chinese women for estimating cervical cancer or its precancerous lesions.
Cervical samples from 215 women infected with high-risk HPV were collected by smear testing. We purposely chose 61 patients with cervical cancer, 57 with high-grade squamous intraepithelial lesions (HSIL), 31 with low-grade squamous intraepithelial lesions (LSIL), and 66 without cervical intraepithelial neoplasia (CIN) after histological confirmation. Taqman probe-based quantitative PCR (qPCR) was utilized to detect the methylation status of FAM19A4 in the cervical samples and further evaluate the use of this gene in the diagnosis of cervical cancer.
(1) An increasing level of FAM19A4 methylation was detected with increasing progression of cervical lesions, with methylation rates of 10.61%(7/66), 35.48%(11/31), 56.14%(32/57) and 93.44%(57/61) in no CIN, LSIL, HSIL and cervical carcinoma samples respectively. (2) In all hrHPV-positive samples, the levels of FAM19A4 methylation in HPV16/18 groups were higher than that in 12 other hrHPV groups (P 0.05). (3)There were no significant differences of FAM19A4 methylation in different clinicopathological parameters of cervical cancer. (4) Though the sensitivity of FAM19A4 methylation test was inferior to that of cytology and FAM19A4 combining with HPV16/18 genotyping, but showed the best specificity with 81.44% both for detection HSIL alone and ≥ HSIL, with favorable youden index (YI) and area under curve (AUC).
FAM19A4 is a specific biomarker of cancerous lesions of the cervix. FAM19A4 methylation analysis may serve as an auxiliary screening method for diagnosis of cervical (pre)cancer. However, in consideration of the limitations of this retrospective study, prospective population-based studies are necessary for further confirmation of the diagnostic value of FAM19A4 methylation for detection of cervical (pre)cancer in Chinese women. |
doi_str_mv | 10.1186/s12885-018-4877-5 |
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Cervical samples from 215 women infected with high-risk HPV were collected by smear testing. We purposely chose 61 patients with cervical cancer, 57 with high-grade squamous intraepithelial lesions (HSIL), 31 with low-grade squamous intraepithelial lesions (LSIL), and 66 without cervical intraepithelial neoplasia (CIN) after histological confirmation. Taqman probe-based quantitative PCR (qPCR) was utilized to detect the methylation status of FAM19A4 in the cervical samples and further evaluate the use of this gene in the diagnosis of cervical cancer.
(1) An increasing level of FAM19A4 methylation was detected with increasing progression of cervical lesions, with methylation rates of 10.61%(7/66), 35.48%(11/31), 56.14%(32/57) and 93.44%(57/61) in no CIN, LSIL, HSIL and cervical carcinoma samples respectively. (2) In all hrHPV-positive samples, the levels of FAM19A4 methylation in HPV16/18 groups were higher than that in 12 other hrHPV groups (P < 0.05), but there was no significant difference between two groups after grouping cervical lesions into cervical cancer, HSIL, LSIL and no CIN groups (P>0.05). (3)There were no significant differences of FAM19A4 methylation in different clinicopathological parameters of cervical cancer. (4) Though the sensitivity of FAM19A4 methylation test was inferior to that of cytology and FAM19A4 combining with HPV16/18 genotyping, but showed the best specificity with 81.44% both for detection HSIL alone and ≥ HSIL, with favorable youden index (YI) and area under curve (AUC).
FAM19A4 is a specific biomarker of cancerous lesions of the cervix. FAM19A4 methylation analysis may serve as an auxiliary screening method for diagnosis of cervical (pre)cancer. However, in consideration of the limitations of this retrospective study, prospective population-based studies are necessary for further confirmation of the diagnostic value of FAM19A4 methylation for detection of cervical (pre)cancer in Chinese women.</description><identifier>ISSN: 1471-2407</identifier><identifier>EISSN: 1471-2407</identifier><identifier>DOI: 10.1186/s12885-018-4877-5</identifier><identifier>PMID: 30486875</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Asian Continental Ancestry Group - genetics ; Biomarkers ; Cancer research ; Cellular biology ; Cervical cancer ; Cervical carcinoma ; Cervix dysplasia ; Cervix Uteri - virology ; Clinical significance ; Complications and side effects ; Cytokines - genetics ; Cytology ; Deoxyribonucleic acid ; Diagnosis ; DNA ; DNA methylation ; DNA Methylation - genetics ; Epigenetics ; FAM19A4 ; Female ; Genetic aspects ; Genotype ; Genotyping ; Health aspects ; Health risk assessment ; HPV genotyping ; Human papillomavirus ; Humans ; Infections ; Medical screening ; Methylation ; Middle Aged ; Papillomaviridae - pathogenicity ; Papillomavirus infections ; Papillomavirus Infections - genetics ; Papillomavirus Infections - virology ; Population studies ; Quantitative PCR (qPCR) ; Retrospective Studies ; Risk ; Studies ; Tumor markers ; Uterine Cervical Neoplasms - genetics ; Uterine Cervical Neoplasms - virology ; Vaginal Smears - methods</subject><ispartof>BMC cancer, 2018-11, Vol.18 (1), p.1182-1182, Article 1182</ispartof><rights>COPYRIGHT 2018 BioMed Central Ltd.</rights><rights>Copyright © 2018. 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). 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c560t-baff104f33f2a8baea114ffced222aa3c215762872cf9af33426223f5eeddcdf3</citedby><cites>FETCH-LOGICAL-c560t-baff104f33f2a8baea114ffced222aa3c215762872cf9af33426223f5eeddcdf3</cites><orcidid>0000-0002-0559-7278</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/PMC6263049/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2158415896?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25752,27923,27924,37011,37012,44589,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30486875$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bu, Qiaowen</creatorcontrib><creatorcontrib>Wang, Sanfeng</creatorcontrib><creatorcontrib>Ma, Jian</creatorcontrib><creatorcontrib>Zhou, Xiangcheng</creatorcontrib><creatorcontrib>Hu, Guiying</creatorcontrib><creatorcontrib>Deng, Hua</creatorcontrib><creatorcontrib>Sun, Xiaoli</creatorcontrib><creatorcontrib>Hong, Xiaoshan</creatorcontrib><creatorcontrib>Wu, Hengying</creatorcontrib><creatorcontrib>Zhang, Liang</creatorcontrib><creatorcontrib>Luo, Xiping</creatorcontrib><title>The clinical significance of FAM19A4 methylation in high-risk HPV-positive cervical samples for the detection of cervical (pre)cancer in Chinese women</title><title>BMC cancer</title><addtitle>BMC Cancer</addtitle><description>To explore the diagnostic value of FAM19A4 methylation in high-risk human papilloma virus (hrHPV)-positive cervical samples from Chinese women for estimating cervical cancer or its precancerous lesions.
Cervical samples from 215 women infected with high-risk HPV were collected by smear testing. We purposely chose 61 patients with cervical cancer, 57 with high-grade squamous intraepithelial lesions (HSIL), 31 with low-grade squamous intraepithelial lesions (LSIL), and 66 without cervical intraepithelial neoplasia (CIN) after histological confirmation. Taqman probe-based quantitative PCR (qPCR) was utilized to detect the methylation status of FAM19A4 in the cervical samples and further evaluate the use of this gene in the diagnosis of cervical cancer.
(1) An increasing level of FAM19A4 methylation was detected with increasing progression of cervical lesions, with methylation rates of 10.61%(7/66), 35.48%(11/31), 56.14%(32/57) and 93.44%(57/61) in no CIN, LSIL, HSIL and cervical carcinoma samples respectively. (2) In all hrHPV-positive samples, the levels of FAM19A4 methylation in HPV16/18 groups were higher than that in 12 other hrHPV groups (P < 0.05), but there was no significant difference between two groups after grouping cervical lesions into cervical cancer, HSIL, LSIL and no CIN groups (P>0.05). (3)There were no significant differences of FAM19A4 methylation in different clinicopathological parameters of cervical cancer. (4) Though the sensitivity of FAM19A4 methylation test was inferior to that of cytology and FAM19A4 combining with HPV16/18 genotyping, but showed the best specificity with 81.44% both for detection HSIL alone and ≥ HSIL, with favorable youden index (YI) and area under curve (AUC).
FAM19A4 is a specific biomarker of cancerous lesions of the cervix. FAM19A4 methylation analysis may serve as an auxiliary screening method for diagnosis of cervical (pre)cancer. However, in consideration of the limitations of this retrospective study, prospective population-based studies are necessary for further confirmation of the diagnostic value of FAM19A4 methylation for detection of cervical (pre)cancer in Chinese women.</description><subject>Asian Continental Ancestry Group - genetics</subject><subject>Biomarkers</subject><subject>Cancer research</subject><subject>Cellular biology</subject><subject>Cervical cancer</subject><subject>Cervical carcinoma</subject><subject>Cervix dysplasia</subject><subject>Cervix Uteri - virology</subject><subject>Clinical significance</subject><subject>Complications and side effects</subject><subject>Cytokines - genetics</subject><subject>Cytology</subject><subject>Deoxyribonucleic acid</subject><subject>Diagnosis</subject><subject>DNA</subject><subject>DNA methylation</subject><subject>DNA Methylation - genetics</subject><subject>Epigenetics</subject><subject>FAM19A4</subject><subject>Female</subject><subject>Genetic aspects</subject><subject>Genotype</subject><subject>Genotyping</subject><subject>Health aspects</subject><subject>Health risk assessment</subject><subject>HPV genotyping</subject><subject>Human papillomavirus</subject><subject>Humans</subject><subject>Infections</subject><subject>Medical screening</subject><subject>Methylation</subject><subject>Middle Aged</subject><subject>Papillomaviridae - pathogenicity</subject><subject>Papillomavirus infections</subject><subject>Papillomavirus Infections - genetics</subject><subject>Papillomavirus Infections - virology</subject><subject>Population studies</subject><subject>Quantitative PCR (qPCR)</subject><subject>Retrospective Studies</subject><subject>Risk</subject><subject>Studies</subject><subject>Tumor markers</subject><subject>Uterine Cervical Neoplasms - genetics</subject><subject>Uterine Cervical Neoplasms - virology</subject><subject>Vaginal Smears - methods</subject><issn>1471-2407</issn><issn>1471-2407</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptktGOEyEUhidG466rD-CNIfFmvZgVGGCYG5Omcd1N1ujF6i1hmEOHOgMVpjX7Ij6vtF2b1hhCOIH__06AvyheE3xFiBTvE6FS8hITWTJZ1yV_UpwTVpOSMlw_ParPihcpLTEmtcTyeXFWYSaFrPl58fu-B2QG553RA0pu4Z3NpTeAgkXXs8-kmTE0wtQ_DHpywSPnUe8WfRld-oFuvn4vVyG5yW0yBuJmj9HjaoCEbIhoyvwOJjA7c2YeVJerCO92reIWOu-dhwToVxjBvyyeWT0kePW4XhTfrj_ez2_Kuy-fbuezu9Jwgaey1dYSzGxVWaplq0ETwqw10FFKta4MJbwWVNbU2EZnGaOC0spygK4zna0uits9twt6qVbRjTo-qKCd2m2EuFA6Ts4MoERrLBGVkARXrGnb1hqstZBScDAYaGZ92LNW63aEzoCfoh5OoKcn3vVqETZKUJE_pMmAy0dADD_XkCY1umRgGLSHsE6KkqrhdcMakaVv_5Euwzr6_FRZxSXL81i10PkCztuQ-5otVM24kBUWjG7bXv1HlUcHozPBg3V5_8RA9gYTQ0oR7OGOBKttMNU-mCoHU22DqXj2vDl-nIPjbxKrP2AH31c</recordid><startdate>20181129</startdate><enddate>20181129</enddate><creator>Bu, Qiaowen</creator><creator>Wang, Sanfeng</creator><creator>Ma, Jian</creator><creator>Zhou, Xiangcheng</creator><creator>Hu, Guiying</creator><creator>Deng, Hua</creator><creator>Sun, Xiaoli</creator><creator>Hong, Xiaoshan</creator><creator>Wu, Hengying</creator><creator>Zhang, Liang</creator><creator>Luo, Xiping</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</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>7TO</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>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-0559-7278</orcidid></search><sort><creationdate>20181129</creationdate><title>The clinical significance of FAM19A4 methylation in high-risk HPV-positive cervical samples for the detection of cervical (pre)cancer in Chinese women</title><author>Bu, Qiaowen ; Wang, Sanfeng ; Ma, Jian ; Zhou, Xiangcheng ; Hu, Guiying ; Deng, Hua ; Sun, Xiaoli ; Hong, Xiaoshan ; Wu, Hengying ; Zhang, Liang ; Luo, Xiping</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c560t-baff104f33f2a8baea114ffced222aa3c215762872cf9af33426223f5eeddcdf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Asian Continental Ancestry Group - genetics</topic><topic>Biomarkers</topic><topic>Cancer research</topic><topic>Cellular biology</topic><topic>Cervical cancer</topic><topic>Cervical carcinoma</topic><topic>Cervix dysplasia</topic><topic>Cervix Uteri - virology</topic><topic>Clinical significance</topic><topic>Complications and side effects</topic><topic>Cytokines - genetics</topic><topic>Cytology</topic><topic>Deoxyribonucleic acid</topic><topic>Diagnosis</topic><topic>DNA</topic><topic>DNA methylation</topic><topic>DNA Methylation - genetics</topic><topic>Epigenetics</topic><topic>FAM19A4</topic><topic>Female</topic><topic>Genetic aspects</topic><topic>Genotype</topic><topic>Genotyping</topic><topic>Health aspects</topic><topic>Health risk assessment</topic><topic>HPV genotyping</topic><topic>Human papillomavirus</topic><topic>Humans</topic><topic>Infections</topic><topic>Medical screening</topic><topic>Methylation</topic><topic>Middle Aged</topic><topic>Papillomaviridae - pathogenicity</topic><topic>Papillomavirus infections</topic><topic>Papillomavirus Infections - genetics</topic><topic>Papillomavirus Infections - virology</topic><topic>Population studies</topic><topic>Quantitative PCR (qPCR)</topic><topic>Retrospective Studies</topic><topic>Risk</topic><topic>Studies</topic><topic>Tumor markers</topic><topic>Uterine Cervical Neoplasms - genetics</topic><topic>Uterine Cervical Neoplasms - virology</topic><topic>Vaginal Smears - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bu, Qiaowen</creatorcontrib><creatorcontrib>Wang, Sanfeng</creatorcontrib><creatorcontrib>Ma, Jian</creatorcontrib><creatorcontrib>Zhou, Xiangcheng</creatorcontrib><creatorcontrib>Hu, Guiying</creatorcontrib><creatorcontrib>Deng, Hua</creatorcontrib><creatorcontrib>Sun, Xiaoli</creatorcontrib><creatorcontrib>Hong, Xiaoshan</creatorcontrib><creatorcontrib>Wu, Hengying</creatorcontrib><creatorcontrib>Zhang, Liang</creatorcontrib><creatorcontrib>Luo, Xiping</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>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medicine (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>ProQuest Central (Alumni Edition)</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</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>PML(ProQuest Medical Library)</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</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><collection>Directory of Open Access Journals</collection><jtitle>BMC cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bu, Qiaowen</au><au>Wang, Sanfeng</au><au>Ma, Jian</au><au>Zhou, Xiangcheng</au><au>Hu, Guiying</au><au>Deng, Hua</au><au>Sun, Xiaoli</au><au>Hong, Xiaoshan</au><au>Wu, Hengying</au><au>Zhang, Liang</au><au>Luo, Xiping</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The clinical significance of FAM19A4 methylation in high-risk HPV-positive cervical samples for the detection of cervical (pre)cancer in Chinese women</atitle><jtitle>BMC cancer</jtitle><addtitle>BMC Cancer</addtitle><date>2018-11-29</date><risdate>2018</risdate><volume>18</volume><issue>1</issue><spage>1182</spage><epage>1182</epage><pages>1182-1182</pages><artnum>1182</artnum><issn>1471-2407</issn><eissn>1471-2407</eissn><abstract>To explore the diagnostic value of FAM19A4 methylation in high-risk human papilloma virus (hrHPV)-positive cervical samples from Chinese women for estimating cervical cancer or its precancerous lesions.
Cervical samples from 215 women infected with high-risk HPV were collected by smear testing. We purposely chose 61 patients with cervical cancer, 57 with high-grade squamous intraepithelial lesions (HSIL), 31 with low-grade squamous intraepithelial lesions (LSIL), and 66 without cervical intraepithelial neoplasia (CIN) after histological confirmation. Taqman probe-based quantitative PCR (qPCR) was utilized to detect the methylation status of FAM19A4 in the cervical samples and further evaluate the use of this gene in the diagnosis of cervical cancer.
(1) An increasing level of FAM19A4 methylation was detected with increasing progression of cervical lesions, with methylation rates of 10.61%(7/66), 35.48%(11/31), 56.14%(32/57) and 93.44%(57/61) in no CIN, LSIL, HSIL and cervical carcinoma samples respectively. (2) In all hrHPV-positive samples, the levels of FAM19A4 methylation in HPV16/18 groups were higher than that in 12 other hrHPV groups (P < 0.05), but there was no significant difference between two groups after grouping cervical lesions into cervical cancer, HSIL, LSIL and no CIN groups (P>0.05). (3)There were no significant differences of FAM19A4 methylation in different clinicopathological parameters of cervical cancer. (4) Though the sensitivity of FAM19A4 methylation test was inferior to that of cytology and FAM19A4 combining with HPV16/18 genotyping, but showed the best specificity with 81.44% both for detection HSIL alone and ≥ HSIL, with favorable youden index (YI) and area under curve (AUC).
FAM19A4 is a specific biomarker of cancerous lesions of the cervix. FAM19A4 methylation analysis may serve as an auxiliary screening method for diagnosis of cervical (pre)cancer. However, in consideration of the limitations of this retrospective study, prospective population-based studies are necessary for further confirmation of the diagnostic value of FAM19A4 methylation for detection of cervical (pre)cancer in Chinese women.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>30486875</pmid><doi>10.1186/s12885-018-4877-5</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-0559-7278</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Asian Continental Ancestry Group - genetics Biomarkers Cancer research Cellular biology Cervical cancer Cervical carcinoma Cervix dysplasia Cervix Uteri - virology Clinical significance Complications and side effects Cytokines - genetics Cytology Deoxyribonucleic acid Diagnosis DNA DNA methylation DNA Methylation - genetics Epigenetics FAM19A4 Female Genetic aspects Genotype Genotyping Health aspects Health risk assessment HPV genotyping Human papillomavirus Humans Infections Medical screening Methylation Middle Aged Papillomaviridae - pathogenicity Papillomavirus infections Papillomavirus Infections - genetics Papillomavirus Infections - virology Population studies Quantitative PCR (qPCR) Retrospective Studies Risk Studies Tumor markers Uterine Cervical Neoplasms - genetics Uterine Cervical Neoplasms - virology Vaginal Smears - methods |
title | The clinical significance of FAM19A4 methylation in high-risk HPV-positive cervical samples for the detection of cervical (pre)cancer in Chinese women |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T11%3A20%3A15IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20clinical%20significance%20of%20FAM19A4%20methylation%20in%20high-risk%20HPV-positive%20cervical%20samples%20for%20the%20detection%20of%20cervical%20(pre)cancer%20in%20Chinese%20women&rft.jtitle=BMC%20cancer&rft.au=Bu,%20Qiaowen&rft.date=2018-11-29&rft.volume=18&rft.issue=1&rft.spage=1182&rft.epage=1182&rft.pages=1182-1182&rft.artnum=1182&rft.issn=1471-2407&rft.eissn=1471-2407&rft_id=info:doi/10.1186/s12885-018-4877-5&rft_dat=%3Cgale_doaj_%3EA568306429%3C/gale_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c560t-baff104f33f2a8baea114ffced222aa3c215762872cf9af33426223f5eeddcdf3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2158415896&rft_id=info:pmid/30486875&rft_galeid=A568306429&rfr_iscdi=true |