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dc.contributor.authorHuang, Tao
dc.contributor.authorWang, Junjie
dc.contributor.authorCai, Yu-Dong
dc.contributor.authorYu, Hanry
dc.contributor.authorChou, Kuo-Chen
dc.date.accessioned2012-07-23T13:39:13Z
dc.date.available2012-07-23T13:39:13Z
dc.date.issued2012-04
dc.date.submitted2011-09
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/1721.1/71745
dc.description.abstractHepatitis C virus (HCV) is a main risk factor for liver cirrhosis and hepatocellular carcinoma, particularly to those patients with chronic liver disease or injury. The similar etiology leads to a high correlation of the patients suffering from the disease of liver cirrhosis with those suffering from the disease of hepatocellular carcinoma. However, the biological mechanism for the relationship between these two kinds of diseases is not clear. The present study was initiated in an attempt to investigate into the HCV infection protein network, in hopes to find good biomarkers for diagnosing the two diseases as well as gain insights into their progression mechanisms. To realize this, two potential biomarker pools were defined: (i) the target genes of HCV, and (ii) the between genes on the shortest paths among the target genes of HCV. Meanwhile, a predictor was developed for identifying the liver tissue samples among the following three categories: (i) normal, (ii) cirrhosis, and (iii) hepatocellular carcinoma. Interestingly, it was observed that the identification accuracy was higher with the tissue samples defined by extracting the features from the second biomarker pool than that with the samples defined based on the first biomarker pool. The identification accuracy by the jackknife validation for the between-genes approach was 0.960, indicating that the novel approach holds a quite promising potential in helping find effective biomarkers for diagnosing the liver cirrhosis disease and the hepatocellular carcinoma disease. It may also provide useful insights for in-depth study of the biological mechanisms of HCV-induced cirrhosis and hepatocellular carcinoma.en_US
dc.description.sponsorshipNational Basic Research Program of China (2011CB510102)en_US
dc.description.sponsorshipNational Basic Research Program of China (2011CB510101)en_US
dc.description.sponsorshipShanghai Municipal Education Commission. (Innovation Program) (12ZZ087)en_US
dc.description.sponsorshipSingapore-MIT Alliance Computational and Systems Biology Flagship Project (C-382-641-001-091)en_US
dc.description.sponsorshipInstitute of Bioengineering and Nanotechnology (Singapore) Jassen Cilag Grant (R-185-000-182-592)en_US
dc.description.sponsorshipSingapore-MIT Alliance for Research and Technology (R-714-001-003-271)en_US
dc.language.isoen_US
dc.publisherPublic Library of Scienceen_US
dc.relation.isversionofhttp://dx.doi.org/10.1371/journal.pone.0034460en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/2.5/en_US
dc.sourcePLoSen_US
dc.titleHepatitis C Virus Network Based Classification of Hepatocellular Cirrhosis and Carcinomaen_US
dc.typeArticleen_US
dc.identifier.citationHuang, Tao et al. “Hepatitis C Virus Network Based Classification of Hepatocellular Cirrhosis and Carcinoma.” Ed. John E. Tavis. PLoS ONE 7.4 (2012): e34460. Wen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.approverYu, Hanry
dc.contributor.mitauthorYu, Hanry
dc.relation.journalPLoS ONEen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsHuang, Tao; Wang, Junjie; Cai, Yu-Dong; Yu, Hanry; Chou, Kuo-Chenen
dc.identifier.orcidhttps://orcid.org/0000-0002-0339-3685
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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