Construction of a 13‐microRNA‐based signature and prognostic nomogram for predicting overall survival in patients with hepatocellular carcinoma

Aim Hepatocellular carcinoma (HCC) is a common malignancy associated with a poor prognosis due to difficulties in reliably estimating overall survival (OS). MicroRNAs (miRNAs) play critical roles in HCC initiation, progression, and metastasis and are highly correlated with patient prognosis. Thus, m...

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Veröffentlicht in:Hepatology research 2020-10, Vol.50 (10), p.1151-1163
Hauptverfasser: Zheng, Zhihua, Wen, Yi, Nie, Kechao, Tang, Shuting, Chen, Xu, Lan, Shaoyang, Pan, Jinglin, Jiang, Kailin, Jiang, Xiaotao, Liu, Peng, Yan, Yanhua, Liu, Fengbin, Liu, Yufeng, Li, Peiwu
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container_end_page 1163
container_issue 10
container_start_page 1151
container_title Hepatology research
container_volume 50
creator Zheng, Zhihua
Wen, Yi
Nie, Kechao
Tang, Shuting
Chen, Xu
Lan, Shaoyang
Pan, Jinglin
Jiang, Kailin
Jiang, Xiaotao
Liu, Peng
Yan, Yanhua
Liu, Fengbin
Liu, Yufeng
Li, Peiwu
description Aim Hepatocellular carcinoma (HCC) is a common malignancy associated with a poor prognosis due to difficulties in reliably estimating overall survival (OS). MicroRNAs (miRNAs) play critical roles in HCC initiation, progression, and metastasis and are highly correlated with patient prognosis. Thus, miRNA‐based risk signatures and nomograms are urgently required for predicting OS in patients with HCC. Methods We constructed a 13‐miRNA‐based signature and prognostic nomogram using 408 HCC samples and 58 normal tissues with miRNA sequencing data and clinical data from 323 patients downloaded from The Cancer Genome Atlas. A total of 195 patients were assigned as the internal validation cohort for verification and testing. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes analysis was applied to investigate pathway enrichment for the signature. Results We identified and validated a 13‐miRNA risk signature highly associating with the OS of HCC patients. The signature showed good performances by calculating C‐index, area under the curve, and calibration curves. After verification and testing using an internal validation cohort, the results yielded a miRNA‐based signature and a prognostic nomogram with reliable predictive accuracy. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes analysis indicated that various genes and multiple pathways were closely related to the mechanisms of HCC proliferation and metastasis. Conclusion We successfully identified a 13‐miRNA‐based signature and prognostic nomogram that are capable of predicting OS in patients with HCC.
doi_str_mv 10.1111/hepr.13538
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MicroRNAs (miRNAs) play critical roles in HCC initiation, progression, and metastasis and are highly correlated with patient prognosis. Thus, miRNA‐based risk signatures and nomograms are urgently required for predicting OS in patients with HCC. Methods We constructed a 13‐miRNA‐based signature and prognostic nomogram using 408 HCC samples and 58 normal tissues with miRNA sequencing data and clinical data from 323 patients downloaded from The Cancer Genome Atlas. A total of 195 patients were assigned as the internal validation cohort for verification and testing. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes analysis was applied to investigate pathway enrichment for the signature. Results We identified and validated a 13‐miRNA risk signature highly associating with the OS of HCC patients. The signature showed good performances by calculating C‐index, area under the curve, and calibration curves. After verification and testing using an internal validation cohort, the results yielded a miRNA‐based signature and a prognostic nomogram with reliable predictive accuracy. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes analysis indicated that various genes and multiple pathways were closely related to the mechanisms of HCC proliferation and metastasis. Conclusion We successfully identified a 13‐miRNA‐based signature and prognostic nomogram that are capable of predicting OS in patients with HCC.</description><identifier>ISSN: 1386-6346</identifier><identifier>EISSN: 1872-034X</identifier><identifier>DOI: 10.1111/hepr.13538</identifier><identifier>PMID: 32567216</identifier><language>eng</language><publisher>HOBOKEN: Wiley</publisher><subject>Gastroenterology &amp; Hepatology ; Genes ; Genomes ; Hepatocellular carcinoma ; Life Sciences &amp; Biomedicine ; Liver cancer ; Malignancy ; Medical prognosis ; Metastases ; Metastasis ; microRNA ; MicroRNAs ; miRNA ; miRNA‐based risk signature ; Ontology ; overall survival ; Prognosis ; prognostic nomogram ; Science &amp; Technology ; Survival</subject><ispartof>Hepatology research, 2020-10, Vol.50 (10), p.1151-1163</ispartof><rights>2020 The Japan Society of Hepatology</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>9</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000559461400001</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c3588-a6836797c44bd8d694720018a1e68b75bbce2fe269b50f3920a971f6974c703c3</citedby><cites>FETCH-LOGICAL-c3588-a6836797c44bd8d694720018a1e68b75bbce2fe269b50f3920a971f6974c703c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fhepr.13538$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fhepr.13538$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,27928,27929,45578,45579</link.rule.ids></links><search><creatorcontrib>Zheng, Zhihua</creatorcontrib><creatorcontrib>Wen, Yi</creatorcontrib><creatorcontrib>Nie, Kechao</creatorcontrib><creatorcontrib>Tang, Shuting</creatorcontrib><creatorcontrib>Chen, Xu</creatorcontrib><creatorcontrib>Lan, Shaoyang</creatorcontrib><creatorcontrib>Pan, Jinglin</creatorcontrib><creatorcontrib>Jiang, Kailin</creatorcontrib><creatorcontrib>Jiang, Xiaotao</creatorcontrib><creatorcontrib>Liu, Peng</creatorcontrib><creatorcontrib>Yan, Yanhua</creatorcontrib><creatorcontrib>Liu, Fengbin</creatorcontrib><creatorcontrib>Liu, Yufeng</creatorcontrib><creatorcontrib>Li, Peiwu</creatorcontrib><title>Construction of a 13‐microRNA‐based signature and prognostic nomogram for predicting overall survival in patients with hepatocellular carcinoma</title><title>Hepatology research</title><addtitle>HEPATOL RES</addtitle><description>Aim Hepatocellular carcinoma (HCC) is a common malignancy associated with a poor prognosis due to difficulties in reliably estimating overall survival (OS). MicroRNAs (miRNAs) play critical roles in HCC initiation, progression, and metastasis and are highly correlated with patient prognosis. Thus, miRNA‐based risk signatures and nomograms are urgently required for predicting OS in patients with HCC. Methods We constructed a 13‐miRNA‐based signature and prognostic nomogram using 408 HCC samples and 58 normal tissues with miRNA sequencing data and clinical data from 323 patients downloaded from The Cancer Genome Atlas. A total of 195 patients were assigned as the internal validation cohort for verification and testing. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes analysis was applied to investigate pathway enrichment for the signature. Results We identified and validated a 13‐miRNA risk signature highly associating with the OS of HCC patients. The signature showed good performances by calculating C‐index, area under the curve, and calibration curves. After verification and testing using an internal validation cohort, the results yielded a miRNA‐based signature and a prognostic nomogram with reliable predictive accuracy. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes analysis indicated that various genes and multiple pathways were closely related to the mechanisms of HCC proliferation and metastasis. 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Wen, Yi ; Nie, Kechao ; Tang, Shuting ; Chen, Xu ; Lan, Shaoyang ; Pan, Jinglin ; Jiang, Kailin ; Jiang, Xiaotao ; Liu, Peng ; Yan, Yanhua ; Liu, Fengbin ; Liu, Yufeng ; Li, Peiwu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3588-a6836797c44bd8d694720018a1e68b75bbce2fe269b50f3920a971f6974c703c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Gastroenterology &amp; Hepatology</topic><topic>Genes</topic><topic>Genomes</topic><topic>Hepatocellular carcinoma</topic><topic>Life Sciences &amp; Biomedicine</topic><topic>Liver cancer</topic><topic>Malignancy</topic><topic>Medical prognosis</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>microRNA</topic><topic>MicroRNAs</topic><topic>miRNA</topic><topic>miRNA‐based risk signature</topic><topic>Ontology</topic><topic>overall survival</topic><topic>Prognosis</topic><topic>prognostic nomogram</topic><topic>Science &amp; Technology</topic><topic>Survival</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zheng, Zhihua</creatorcontrib><creatorcontrib>Wen, Yi</creatorcontrib><creatorcontrib>Nie, Kechao</creatorcontrib><creatorcontrib>Tang, Shuting</creatorcontrib><creatorcontrib>Chen, Xu</creatorcontrib><creatorcontrib>Lan, Shaoyang</creatorcontrib><creatorcontrib>Pan, Jinglin</creatorcontrib><creatorcontrib>Jiang, Kailin</creatorcontrib><creatorcontrib>Jiang, Xiaotao</creatorcontrib><creatorcontrib>Liu, Peng</creatorcontrib><creatorcontrib>Yan, Yanhua</creatorcontrib><creatorcontrib>Liu, Fengbin</creatorcontrib><creatorcontrib>Liu, Yufeng</creatorcontrib><creatorcontrib>Li, Peiwu</creatorcontrib><collection>Web of Science - Science Citation Index Expanded - 2020</collection><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Hepatology research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zheng, Zhihua</au><au>Wen, Yi</au><au>Nie, Kechao</au><au>Tang, Shuting</au><au>Chen, Xu</au><au>Lan, Shaoyang</au><au>Pan, Jinglin</au><au>Jiang, Kailin</au><au>Jiang, Xiaotao</au><au>Liu, Peng</au><au>Yan, Yanhua</au><au>Liu, Fengbin</au><au>Liu, Yufeng</au><au>Li, Peiwu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Construction of a 13‐microRNA‐based signature and prognostic nomogram for predicting overall survival in patients with hepatocellular carcinoma</atitle><jtitle>Hepatology research</jtitle><stitle>HEPATOL RES</stitle><date>2020-10</date><risdate>2020</risdate><volume>50</volume><issue>10</issue><spage>1151</spage><epage>1163</epage><pages>1151-1163</pages><issn>1386-6346</issn><eissn>1872-034X</eissn><abstract>Aim Hepatocellular carcinoma (HCC) is a common malignancy associated with a poor prognosis due to difficulties in reliably estimating overall survival (OS). MicroRNAs (miRNAs) play critical roles in HCC initiation, progression, and metastasis and are highly correlated with patient prognosis. Thus, miRNA‐based risk signatures and nomograms are urgently required for predicting OS in patients with HCC. Methods We constructed a 13‐miRNA‐based signature and prognostic nomogram using 408 HCC samples and 58 normal tissues with miRNA sequencing data and clinical data from 323 patients downloaded from The Cancer Genome Atlas. A total of 195 patients were assigned as the internal validation cohort for verification and testing. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes analysis was applied to investigate pathway enrichment for the signature. Results We identified and validated a 13‐miRNA risk signature highly associating with the OS of HCC patients. The signature showed good performances by calculating C‐index, area under the curve, and calibration curves. After verification and testing using an internal validation cohort, the results yielded a miRNA‐based signature and a prognostic nomogram with reliable predictive accuracy. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes analysis indicated that various genes and multiple pathways were closely related to the mechanisms of HCC proliferation and metastasis. Conclusion We successfully identified a 13‐miRNA‐based signature and prognostic nomogram that are capable of predicting OS in patients with HCC.</abstract><cop>HOBOKEN</cop><pub>Wiley</pub><pmid>32567216</pmid><doi>10.1111/hepr.13538</doi><tpages>13</tpages></addata></record>
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subjects Gastroenterology & Hepatology
Genes
Genomes
Hepatocellular carcinoma
Life Sciences & Biomedicine
Liver cancer
Malignancy
Medical prognosis
Metastases
Metastasis
microRNA
MicroRNAs
miRNA
miRNA‐based risk signature
Ontology
overall survival
Prognosis
prognostic nomogram
Science & Technology
Survival
title Construction of a 13‐microRNA‐based signature and prognostic nomogram for predicting overall survival in patients with hepatocellular carcinoma
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