Serum miR-483-5p as a potential biomarker to detect hepatocellular carcinoma

Background and goals There are no highly sensitive and specific minimally invasive biomarkers for hepatocellular carcinoma (HCC) to date. The objective of this study was to identify serum microRNAs (miRNAs) as potential HCC biomarkers. Methods Using miRCURY LNA™ microRNA arrays, the levels of circul...

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Veröffentlicht in:Hepatology international 2013-03, Vol.7 (1), p.199-207
Hauptverfasser: Zhang, Zhoujing, Ge, Shengxiang, Wang, Xiaomin, Yuan, Quan, Yan, Qiang, Ye, Huiming, Che, Yaojian, Lin, Yanyan, Zhang, Jun, Liu, Pingguo
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container_end_page 207
container_issue 1
container_start_page 199
container_title Hepatology international
container_volume 7
creator Zhang, Zhoujing
Ge, Shengxiang
Wang, Xiaomin
Yuan, Quan
Yan, Qiang
Ye, Huiming
Che, Yaojian
Lin, Yanyan
Zhang, Jun
Liu, Pingguo
description Background and goals There are no highly sensitive and specific minimally invasive biomarkers for hepatocellular carcinoma (HCC) to date. The objective of this study was to identify serum microRNAs (miRNAs) as potential HCC biomarkers. Methods Using miRCURY LNA™ microRNA arrays, the levels of circulating miRNAs in the serum of patients with HCC were compared and controls were matched. Then 253 subjects (112 HCC, 85 chronic hepatitis B [CHB], and 56 healthy controls) were recruited and 12 serum miRNAs were compared by quantitative real-time polymerase chain reaction (qRT-PCR). It was followed by the comparison of serum miRNA concentrations before and after the surgical resection in HCC group. Results Median levels of miR-483-5p and miR-500a were higher in HCC patients than in patients with CHB and in healthy controls ( p   0.05) and miR-483-5p levels were significantly reduced in serum samples obtained 30 days after surgical resection ( p  
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The objective of this study was to identify serum microRNAs (miRNAs) as potential HCC biomarkers. Methods Using miRCURY LNA™ microRNA arrays, the levels of circulating miRNAs in the serum of patients with HCC were compared and controls were matched. Then 253 subjects (112 HCC, 85 chronic hepatitis B [CHB], and 56 healthy controls) were recruited and 12 serum miRNAs were compared by quantitative real-time polymerase chain reaction (qRT-PCR). It was followed by the comparison of serum miRNA concentrations before and after the surgical resection in HCC group. Results Median levels of miR-483-5p and miR-500a were higher in HCC patients than in patients with CHB and in healthy controls ( p  &lt; 0.0001), but there were no differences between CHB patients and healthy controls ( p  &gt; 0.05) and miR-483-5p levels were significantly reduced in serum samples obtained 30 days after surgical resection ( p  &lt; 0.0001). The area under receiver operating characteristic curves of miR-483-5p and miR-500a was 74% (cutoff [Ct] value = 2.824, sensitivity = 74%, and specificity = 66%) and 66% (Ct value = 1.830, sensitivity = 74%, and specificity = 51%) for the prediction of HCC, respectively. In detecting HCC, combining α -fetoprotein (AFP) and serum miR-483-5p (sensitivity = 81% and specificity = 83%) was better than AFP alone (sensitivity = 78%, specificity = 70%). Conclusion Our observations suggest that serum miR-483-5p and miR-500a might serve as novel, noninvasive biomarkers for HCC. Serum miR-483-5p might complement AFP in detecting HCC.</description><identifier>ISSN: 1936-0533</identifier><identifier>EISSN: 1936-0541</identifier><identifier>DOI: 10.1007/s12072-012-9341-z</identifier><identifier>PMID: 26201634</identifier><language>eng</language><publisher>India: Springer-Verlag</publisher><subject>Colorectal Surgery ; Hepatology ; Medicine ; Medicine &amp; Public Health ; Original Article ; Surgery</subject><ispartof>Hepatology international, 2013-03, Vol.7 (1), p.199-207</ispartof><rights>Asian Pacific Association for the Study of the Liver 2012</rights><rights>Asian Pacific Association for the Study of the Liver 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c481t-6c12bf0ca3acc729d3ba1b8896a3b16cbc4fe232b0121caeed21fde7b07c4b723</citedby><cites>FETCH-LOGICAL-c481t-6c12bf0ca3acc729d3ba1b8896a3b16cbc4fe232b0121caeed21fde7b07c4b723</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s12072-012-9341-z$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s12072-012-9341-z$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26201634$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Zhoujing</creatorcontrib><creatorcontrib>Ge, Shengxiang</creatorcontrib><creatorcontrib>Wang, Xiaomin</creatorcontrib><creatorcontrib>Yuan, Quan</creatorcontrib><creatorcontrib>Yan, Qiang</creatorcontrib><creatorcontrib>Ye, Huiming</creatorcontrib><creatorcontrib>Che, Yaojian</creatorcontrib><creatorcontrib>Lin, Yanyan</creatorcontrib><creatorcontrib>Zhang, Jun</creatorcontrib><creatorcontrib>Liu, Pingguo</creatorcontrib><title>Serum miR-483-5p as a potential biomarker to detect hepatocellular carcinoma</title><title>Hepatology international</title><addtitle>Hepatol Int</addtitle><addtitle>Hepatol Int</addtitle><description>Background and goals There are no highly sensitive and specific minimally invasive biomarkers for hepatocellular carcinoma (HCC) to date. The objective of this study was to identify serum microRNAs (miRNAs) as potential HCC biomarkers. Methods Using miRCURY LNA™ microRNA arrays, the levels of circulating miRNAs in the serum of patients with HCC were compared and controls were matched. Then 253 subjects (112 HCC, 85 chronic hepatitis B [CHB], and 56 healthy controls) were recruited and 12 serum miRNAs were compared by quantitative real-time polymerase chain reaction (qRT-PCR). It was followed by the comparison of serum miRNA concentrations before and after the surgical resection in HCC group. Results Median levels of miR-483-5p and miR-500a were higher in HCC patients than in patients with CHB and in healthy controls ( p  &lt; 0.0001), but there were no differences between CHB patients and healthy controls ( p  &gt; 0.05) and miR-483-5p levels were significantly reduced in serum samples obtained 30 days after surgical resection ( p  &lt; 0.0001). The area under receiver operating characteristic curves of miR-483-5p and miR-500a was 74% (cutoff [Ct] value = 2.824, sensitivity = 74%, and specificity = 66%) and 66% (Ct value = 1.830, sensitivity = 74%, and specificity = 51%) for the prediction of HCC, respectively. In detecting HCC, combining α -fetoprotein (AFP) and serum miR-483-5p (sensitivity = 81% and specificity = 83%) was better than AFP alone (sensitivity = 78%, specificity = 70%). Conclusion Our observations suggest that serum miR-483-5p and miR-500a might serve as novel, noninvasive biomarkers for HCC. Serum miR-483-5p might complement AFP in detecting HCC.</description><subject>Colorectal Surgery</subject><subject>Hepatology</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Original Article</subject><subject>Surgery</subject><issn>1936-0533</issn><issn>1936-0541</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp1kEtLxTAQhYMovn-AGwm4cRPNJG3SLkV8wQXBxzok6VSrfZm0C_315nJVRHA1A_PNmTOHkAPgJ8C5Po0guBaMg2ClzIB9rJFtKKViPM9g_aeXcovsxPjCeZ4rUJtkSyjBQclsmyzuMcwd7Zo7lhWS5SO1kVo6DhP2U2Nb6pqhs-EVA50GWuGEfqLPONpp8Ni2c2sD9Tb4pk_YHtmobRtx_6vuksfLi4fza7a4vbo5P1swnxUwMeVBuJp7K633WpSVdBZcUZTKSgfKO5_VKKRw6THwFrESUFeoHdc-c1rIXXK80h3D8DZjnEzXxKUd2-MwRwOqLLOiLLRM6NEf9GWYQ5_cGZCgNYdS54mCFeXDEGPA2oyhSW-_G-BmGbVZRW2SI7OM2nykncMv5dl1WP1sfGebALECYhr1Txh-nf5X9RMma4kE</recordid><startdate>20130301</startdate><enddate>20130301</enddate><creator>Zhang, Zhoujing</creator><creator>Ge, Shengxiang</creator><creator>Wang, Xiaomin</creator><creator>Yuan, Quan</creator><creator>Yan, Qiang</creator><creator>Ye, Huiming</creator><creator>Che, Yaojian</creator><creator>Lin, Yanyan</creator><creator>Zhang, Jun</creator><creator>Liu, Pingguo</creator><general>Springer-Verlag</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7U7</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope></search><sort><creationdate>20130301</creationdate><title>Serum miR-483-5p as a potential biomarker to detect hepatocellular carcinoma</title><author>Zhang, Zhoujing ; 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Allied Health Database (Alumni Edition)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing &amp; Allied Health Premium</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><jtitle>Hepatology international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Zhoujing</au><au>Ge, Shengxiang</au><au>Wang, Xiaomin</au><au>Yuan, Quan</au><au>Yan, Qiang</au><au>Ye, Huiming</au><au>Che, Yaojian</au><au>Lin, Yanyan</au><au>Zhang, Jun</au><au>Liu, Pingguo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serum miR-483-5p as a potential biomarker to detect hepatocellular carcinoma</atitle><jtitle>Hepatology international</jtitle><stitle>Hepatol Int</stitle><addtitle>Hepatol Int</addtitle><date>2013-03-01</date><risdate>2013</risdate><volume>7</volume><issue>1</issue><spage>199</spage><epage>207</epage><pages>199-207</pages><issn>1936-0533</issn><eissn>1936-0541</eissn><abstract>Background and goals There are no highly sensitive and specific minimally invasive biomarkers for hepatocellular carcinoma (HCC) to date. The objective of this study was to identify serum microRNAs (miRNAs) as potential HCC biomarkers. Methods Using miRCURY LNA™ microRNA arrays, the levels of circulating miRNAs in the serum of patients with HCC were compared and controls were matched. Then 253 subjects (112 HCC, 85 chronic hepatitis B [CHB], and 56 healthy controls) were recruited and 12 serum miRNAs were compared by quantitative real-time polymerase chain reaction (qRT-PCR). It was followed by the comparison of serum miRNA concentrations before and after the surgical resection in HCC group. Results Median levels of miR-483-5p and miR-500a were higher in HCC patients than in patients with CHB and in healthy controls ( p  &lt; 0.0001), but there were no differences between CHB patients and healthy controls ( p  &gt; 0.05) and miR-483-5p levels were significantly reduced in serum samples obtained 30 days after surgical resection ( p  &lt; 0.0001). The area under receiver operating characteristic curves of miR-483-5p and miR-500a was 74% (cutoff [Ct] value = 2.824, sensitivity = 74%, and specificity = 66%) and 66% (Ct value = 1.830, sensitivity = 74%, and specificity = 51%) for the prediction of HCC, respectively. In detecting HCC, combining α -fetoprotein (AFP) and serum miR-483-5p (sensitivity = 81% and specificity = 83%) was better than AFP alone (sensitivity = 78%, specificity = 70%). Conclusion Our observations suggest that serum miR-483-5p and miR-500a might serve as novel, noninvasive biomarkers for HCC. Serum miR-483-5p might complement AFP in detecting HCC.</abstract><cop>India</cop><pub>Springer-Verlag</pub><pmid>26201634</pmid><doi>10.1007/s12072-012-9341-z</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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subjects Colorectal Surgery
Hepatology
Medicine
Medicine & Public Health
Original Article
Surgery
title Serum miR-483-5p as a potential biomarker to detect hepatocellular carcinoma
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