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Metabolomic Characterization of Hepatocellular Carcinoma in Patients with Liver Cirrhosis for Biomarker Discovery
Metabolomics plays an important role in providing insight into the etiology and mechanisms of hepatocellular carcinoma (HCC). This is accomplished by a comprehensive analysis of patterns involved in metabolic alterations in human specimens. This study compares the levels of plasma metabolites in HCC...
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Published in: | Cancer epidemiology, biomarkers & prevention biomarkers & prevention, 2017-05, Vol.26 (5), p.675-683 |
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creator | Di Poto, Cristina Ferrarini, Alessia Zhao, Yi Varghese, Rency S Tu, Chao Zuo, Yiming Wang, Minkun Nezami Ranjbar, Mohammad R Luo, Yue Zhang, Chi Desai, Chirag S Shetty, Kirti Tadesse, Mahlet G Ressom, Habtom W |
description | Metabolomics plays an important role in providing insight into the etiology and mechanisms of hepatocellular carcinoma (HCC). This is accomplished by a comprehensive analysis of patterns involved in metabolic alterations in human specimens. This study compares the levels of plasma metabolites in HCC cases versus cirrhotic patients and evaluates the ability of candidate metabolites in distinguishing the two groups. Also, it investigates the combined use of metabolites and clinical covariates for detection of HCC in patients with liver cirrhosis.
Untargeted analysis of metabolites in plasma from 128 subjects (63 HCC cases and 65 cirrhotic controls) was conducted using gas chromatography coupled to mass spectrometry (GC-MS). This was followed by targeted evaluation of selected metabolites. LASSO regression was used to select a set of metabolites and clinical covariates that are associated with HCC. The performance of candidate biomarkers in distinguishing HCC from cirrhosis was evaluated through a leave-one-out cross-validation based on area under the receiver operating characteristics (ROC) curve.
We identified 11 metabolites and three clinical covariates that differentiated HCC cases from cirrhotic controls. Combining these features in a panel for disease classification using support vector machines (SVM) yielded better area under the ROC curve compared with alpha-fetoprotein (AFP).
This study demonstrates the combination of metabolites and clinical covariates as an effective approach for early detection of HCC in patients with liver cirrhosis.
Further investigation of these findings may improve understanding of HCC pathophysiology and possible implication of the metabolites in HCC prevention and diagnosis.
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doi_str_mv | 10.1158/1055-9965.EPI-16-0366 |
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Untargeted analysis of metabolites in plasma from 128 subjects (63 HCC cases and 65 cirrhotic controls) was conducted using gas chromatography coupled to mass spectrometry (GC-MS). This was followed by targeted evaluation of selected metabolites. LASSO regression was used to select a set of metabolites and clinical covariates that are associated with HCC. The performance of candidate biomarkers in distinguishing HCC from cirrhosis was evaluated through a leave-one-out cross-validation based on area under the receiver operating characteristics (ROC) curve.
We identified 11 metabolites and three clinical covariates that differentiated HCC cases from cirrhotic controls. Combining these features in a panel for disease classification using support vector machines (SVM) yielded better area under the ROC curve compared with alpha-fetoprotein (AFP).
This study demonstrates the combination of metabolites and clinical covariates as an effective approach for early detection of HCC in patients with liver cirrhosis.
Further investigation of these findings may improve understanding of HCC pathophysiology and possible implication of the metabolites in HCC prevention and diagnosis.
.</description><identifier>ISSN: 1055-9965</identifier><identifier>EISSN: 1538-7755</identifier><identifier>DOI: 10.1158/1055-9965.EPI-16-0366</identifier><identifier>PMID: 27913395</identifier><language>eng</language><publisher>United States: American Association for Cancer Research, Inc</publisher><subject>Adult ; Aged ; Biomarkers ; Biomarkers, Tumor - blood ; Carcinoma, Hepatocellular - blood ; Carcinoma, Hepatocellular - diagnosis ; Cirrhosis ; Etiology ; Female ; Gas chromatography ; Hepatocellular carcinoma ; Humans ; Liver ; Liver cancer ; Liver cirrhosis ; Liver Cirrhosis - blood ; Liver Cirrhosis - diagnosis ; Liver Neoplasms - blood ; Liver Neoplasms - diagnosis ; Male ; Mass spectrometry ; Mass spectroscopy ; Metabolites ; Metabolomics ; Metabolomics - methods ; Middle Aged ; Sensitivity and Specificity ; α-Fetoprotein</subject><ispartof>Cancer epidemiology, biomarkers & prevention, 2017-05, Vol.26 (5), p.675-683</ispartof><rights>2016 American Association for Cancer Research.</rights><rights>Copyright American Association for Cancer Research, Inc. May 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c472t-2f9e377f7c9354527993b148c4026ac34e77f4c7717b7fb8199e4d6aab550403</citedby><cites>FETCH-LOGICAL-c472t-2f9e377f7c9354527993b148c4026ac34e77f4c7717b7fb8199e4d6aab550403</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,777,781,882,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27913395$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Di Poto, Cristina</creatorcontrib><creatorcontrib>Ferrarini, Alessia</creatorcontrib><creatorcontrib>Zhao, Yi</creatorcontrib><creatorcontrib>Varghese, Rency S</creatorcontrib><creatorcontrib>Tu, Chao</creatorcontrib><creatorcontrib>Zuo, Yiming</creatorcontrib><creatorcontrib>Wang, Minkun</creatorcontrib><creatorcontrib>Nezami Ranjbar, Mohammad R</creatorcontrib><creatorcontrib>Luo, Yue</creatorcontrib><creatorcontrib>Zhang, Chi</creatorcontrib><creatorcontrib>Desai, Chirag S</creatorcontrib><creatorcontrib>Shetty, Kirti</creatorcontrib><creatorcontrib>Tadesse, Mahlet G</creatorcontrib><creatorcontrib>Ressom, Habtom W</creatorcontrib><title>Metabolomic Characterization of Hepatocellular Carcinoma in Patients with Liver Cirrhosis for Biomarker Discovery</title><title>Cancer epidemiology, biomarkers & prevention</title><addtitle>Cancer Epidemiol Biomarkers Prev</addtitle><description>Metabolomics plays an important role in providing insight into the etiology and mechanisms of hepatocellular carcinoma (HCC). This is accomplished by a comprehensive analysis of patterns involved in metabolic alterations in human specimens. This study compares the levels of plasma metabolites in HCC cases versus cirrhotic patients and evaluates the ability of candidate metabolites in distinguishing the two groups. Also, it investigates the combined use of metabolites and clinical covariates for detection of HCC in patients with liver cirrhosis.
Untargeted analysis of metabolites in plasma from 128 subjects (63 HCC cases and 65 cirrhotic controls) was conducted using gas chromatography coupled to mass spectrometry (GC-MS). This was followed by targeted evaluation of selected metabolites. LASSO regression was used to select a set of metabolites and clinical covariates that are associated with HCC. The performance of candidate biomarkers in distinguishing HCC from cirrhosis was evaluated through a leave-one-out cross-validation based on area under the receiver operating characteristics (ROC) curve.
We identified 11 metabolites and three clinical covariates that differentiated HCC cases from cirrhotic controls. Combining these features in a panel for disease classification using support vector machines (SVM) yielded better area under the ROC curve compared with alpha-fetoprotein (AFP).
This study demonstrates the combination of metabolites and clinical covariates as an effective approach for early detection of HCC in patients with liver cirrhosis.
Further investigation of these findings may improve understanding of HCC pathophysiology and possible implication of the metabolites in HCC prevention and diagnosis.
.</description><subject>Adult</subject><subject>Aged</subject><subject>Biomarkers</subject><subject>Biomarkers, Tumor - blood</subject><subject>Carcinoma, Hepatocellular - blood</subject><subject>Carcinoma, Hepatocellular - diagnosis</subject><subject>Cirrhosis</subject><subject>Etiology</subject><subject>Female</subject><subject>Gas chromatography</subject><subject>Hepatocellular carcinoma</subject><subject>Humans</subject><subject>Liver</subject><subject>Liver cancer</subject><subject>Liver cirrhosis</subject><subject>Liver Cirrhosis - blood</subject><subject>Liver Cirrhosis - diagnosis</subject><subject>Liver Neoplasms - blood</subject><subject>Liver Neoplasms - diagnosis</subject><subject>Male</subject><subject>Mass spectrometry</subject><subject>Mass spectroscopy</subject><subject>Metabolites</subject><subject>Metabolomics</subject><subject>Metabolomics - methods</subject><subject>Middle Aged</subject><subject>Sensitivity and Specificity</subject><subject>α-Fetoprotein</subject><issn>1055-9965</issn><issn>1538-7755</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNqNkUtP3TAQhS3Uqrz6E0CWumETaseeON4glctTuhUs2FuOcbiG3PhiJxfBr2ciHmq76sqW55vjM3MI2ePskHOof3IGUGhdweHp9WXBq4KJqtogWxxEXSgF8AXvH8wm2c75njGmNMA3slkqzYXQsEUef_vBNrGLy-DobGGTdYNP4cUOIfY0tvTCr-wQne-6sbOJzmxyoY9LS0NPr5Hy_ZDpUxgWdB7WHoGQ0iLmkGkbEz0OiKYHfD8J2UUEnnfJ19Z22X9_P3fIzdnpzeyimF-dX85-zQsnVTkUZau9UKpVTguQgI61aLisnWRlZZ2QHovSKcVVo9qm5lp7eVtZ2wAwycQOOXqTXY3N0t869JlsZ1YpoKFnE20wf1f6sDB3cW1AciFliQIH7wIpPo4-D2aJI-AebO_jmA2vtRKKlUL_ByqhFhWvJ1s__kHv45h6XIThuhYlcuX0N7xRLsWck28_fXNmpvjNFK2ZojUYv-GVmeLHvv0_h_7s-shbvALg76zu</recordid><startdate>20170501</startdate><enddate>20170501</enddate><creator>Di Poto, Cristina</creator><creator>Ferrarini, Alessia</creator><creator>Zhao, Yi</creator><creator>Varghese, Rency S</creator><creator>Tu, Chao</creator><creator>Zuo, Yiming</creator><creator>Wang, Minkun</creator><creator>Nezami Ranjbar, Mohammad R</creator><creator>Luo, Yue</creator><creator>Zhang, Chi</creator><creator>Desai, Chirag S</creator><creator>Shetty, Kirti</creator><creator>Tadesse, Mahlet G</creator><creator>Ressom, Habtom W</creator><general>American Association for Cancer Research, Inc</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>7TM</scope><scope>7TO</scope><scope>H94</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20170501</creationdate><title>Metabolomic Characterization of Hepatocellular Carcinoma in Patients with Liver Cirrhosis for Biomarker Discovery</title><author>Di Poto, Cristina ; Ferrarini, Alessia ; Zhao, Yi ; Varghese, Rency S ; Tu, Chao ; Zuo, Yiming ; Wang, Minkun ; Nezami Ranjbar, Mohammad R ; Luo, Yue ; Zhang, Chi ; Desai, Chirag S ; Shetty, Kirti ; Tadesse, Mahlet G ; Ressom, Habtom W</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c472t-2f9e377f7c9354527993b148c4026ac34e77f4c7717b7fb8199e4d6aab550403</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Biomarkers</topic><topic>Biomarkers, Tumor - blood</topic><topic>Carcinoma, Hepatocellular - blood</topic><topic>Carcinoma, Hepatocellular - diagnosis</topic><topic>Cirrhosis</topic><topic>Etiology</topic><topic>Female</topic><topic>Gas chromatography</topic><topic>Hepatocellular carcinoma</topic><topic>Humans</topic><topic>Liver</topic><topic>Liver cancer</topic><topic>Liver cirrhosis</topic><topic>Liver Cirrhosis - blood</topic><topic>Liver Cirrhosis - diagnosis</topic><topic>Liver Neoplasms - blood</topic><topic>Liver Neoplasms - diagnosis</topic><topic>Male</topic><topic>Mass spectrometry</topic><topic>Mass spectroscopy</topic><topic>Metabolites</topic><topic>Metabolomics</topic><topic>Metabolomics - methods</topic><topic>Middle Aged</topic><topic>Sensitivity and Specificity</topic><topic>α-Fetoprotein</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Di Poto, Cristina</creatorcontrib><creatorcontrib>Ferrarini, Alessia</creatorcontrib><creatorcontrib>Zhao, Yi</creatorcontrib><creatorcontrib>Varghese, Rency S</creatorcontrib><creatorcontrib>Tu, Chao</creatorcontrib><creatorcontrib>Zuo, Yiming</creatorcontrib><creatorcontrib>Wang, Minkun</creatorcontrib><creatorcontrib>Nezami Ranjbar, Mohammad R</creatorcontrib><creatorcontrib>Luo, Yue</creatorcontrib><creatorcontrib>Zhang, Chi</creatorcontrib><creatorcontrib>Desai, Chirag S</creatorcontrib><creatorcontrib>Shetty, Kirti</creatorcontrib><creatorcontrib>Tadesse, Mahlet G</creatorcontrib><creatorcontrib>Ressom, Habtom W</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancer epidemiology, biomarkers & prevention</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Di Poto, Cristina</au><au>Ferrarini, Alessia</au><au>Zhao, Yi</au><au>Varghese, Rency S</au><au>Tu, Chao</au><au>Zuo, Yiming</au><au>Wang, Minkun</au><au>Nezami Ranjbar, Mohammad R</au><au>Luo, Yue</au><au>Zhang, Chi</au><au>Desai, Chirag S</au><au>Shetty, Kirti</au><au>Tadesse, Mahlet G</au><au>Ressom, Habtom W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metabolomic Characterization of Hepatocellular Carcinoma in Patients with Liver Cirrhosis for Biomarker Discovery</atitle><jtitle>Cancer epidemiology, biomarkers & prevention</jtitle><addtitle>Cancer Epidemiol Biomarkers Prev</addtitle><date>2017-05-01</date><risdate>2017</risdate><volume>26</volume><issue>5</issue><spage>675</spage><epage>683</epage><pages>675-683</pages><issn>1055-9965</issn><eissn>1538-7755</eissn><abstract>Metabolomics plays an important role in providing insight into the etiology and mechanisms of hepatocellular carcinoma (HCC). This is accomplished by a comprehensive analysis of patterns involved in metabolic alterations in human specimens. This study compares the levels of plasma metabolites in HCC cases versus cirrhotic patients and evaluates the ability of candidate metabolites in distinguishing the two groups. Also, it investigates the combined use of metabolites and clinical covariates for detection of HCC in patients with liver cirrhosis.
Untargeted analysis of metabolites in plasma from 128 subjects (63 HCC cases and 65 cirrhotic controls) was conducted using gas chromatography coupled to mass spectrometry (GC-MS). This was followed by targeted evaluation of selected metabolites. LASSO regression was used to select a set of metabolites and clinical covariates that are associated with HCC. The performance of candidate biomarkers in distinguishing HCC from cirrhosis was evaluated through a leave-one-out cross-validation based on area under the receiver operating characteristics (ROC) curve.
We identified 11 metabolites and three clinical covariates that differentiated HCC cases from cirrhotic controls. Combining these features in a panel for disease classification using support vector machines (SVM) yielded better area under the ROC curve compared with alpha-fetoprotein (AFP).
This study demonstrates the combination of metabolites and clinical covariates as an effective approach for early detection of HCC in patients with liver cirrhosis.
Further investigation of these findings may improve understanding of HCC pathophysiology and possible implication of the metabolites in HCC prevention and diagnosis.
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subjects | Adult Aged Biomarkers Biomarkers, Tumor - blood Carcinoma, Hepatocellular - blood Carcinoma, Hepatocellular - diagnosis Cirrhosis Etiology Female Gas chromatography Hepatocellular carcinoma Humans Liver Liver cancer Liver cirrhosis Liver Cirrhosis - blood Liver Cirrhosis - diagnosis Liver Neoplasms - blood Liver Neoplasms - diagnosis Male Mass spectrometry Mass spectroscopy Metabolites Metabolomics Metabolomics - methods Middle Aged Sensitivity and Specificity α-Fetoprotein |
title | Metabolomic Characterization of Hepatocellular Carcinoma in Patients with Liver Cirrhosis for Biomarker Discovery |
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