<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lu Y</submitter><funding>Chinese Academy of Sciences</funding><funding>Shanghai Committee of Science and Technology</funding><funding>E-Institutes of Shanghai Municipal Education Commission</funding><funding>National Science and Technology Major Project of China</funding><funding>National Natural Science Foundation of China</funding><funding>National Key Research and Development Program of China</funding><pagination>665-677</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6788726</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(8)</volume><pubmed_abstract>Hepatitis B virus (HBV)-induced hepatocellular carcinoma (HCC) is a major cause of cancer-related deaths in Asia and Africa. Developing effective and non-invasive biomarkers of HCC for individual patients remains an urgent task for early diagnosis and convenient monitoring. Analyzing the transcriptomic profiles of peripheral blood mononuclear cells from both healthy donors and patients with chronic HBV infection in different states (i.e. HBV carrier, chronic hepatitis B, cirrhosis, and HCC), we identified a set of 19 candidate genes according to our algorithm of dynamic network biomarkers. These genes can both characterize different stages during HCC progression and identify cirrhosis as the critical transition stage before carcinogenesis. The interaction effects (i.e. co-expressions) of c</pubmed_abstract><journal>Journal of molecular cell biology</journal><pubmed_title>Dynamic edge-based biomarker non-invasively predicts hepatocellular carcinoma with hepatitis B virus infection for individual patients based on blood testing.</pubmed_title><pmcid>PMC6788726</pmcid><funding_grant_id>2017YFA0505500</funding_grant_id><funding_grant_id>81473443</funding_grant_id><funding_grant_id>XDB13040700</funding_grant_id><funding_grant_id>14YF1411400</funding_grant_id><funding_grant_id>31771476</funding_grant_id><funding_grant_id>81503478</funding_grant_id><funding_grant_id>2012ZX10005001-004</funding_grant_id><funding_grant_id>E03008</funding_grant_id><funding_grant_id>18YF1420700</funding_grant_id><pubmed_authors>Chen Q</pubmed_authors><pubmed_authors>Zhou Q</pubmed_authors><pubmed_authors>Hu Y</pubmed_authors><pubmed_authors>Lu Y</pubmed_authors><pubmed_authors>Zhang H</pubmed_authors><pubmed_authors>Chen L</pubmed_authors><pubmed_authors>Sun Y</pubmed_authors><pubmed_authors>Li M</pubmed_authors><pubmed_authors>Zeng T</pubmed_authors><pubmed_authors>Xue X</pubmed_authors><pubmed_authors>Lu L</pubmed_authors><pubmed_authors>Su S</pubmed_authors><pubmed_authors>Fang Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>Dynamic edge-based biomarker non-invasively predicts hepatocellular carcinoma with hepatitis B virus infection for individual patients based on blood testing.</name><description>Hepatitis B virus (HBV)-induced hepatocellular carcinoma (HCC) is a major cause of cancer-related deaths in Asia and Africa. Developing effective and non-invasive biomarkers of HCC for individual patients remains an urgent task for early diagnosis and convenient monitoring. Analyzing the transcriptomic profiles of peripheral blood mononuclear cells from both healthy donors and patients with chronic HBV infection in different states (i.e. HBV carrier, chronic hepatitis B, cirrhosis, and HCC), we identified a set of 19 candidate genes according to our algorithm of dynamic network biomarkers. These genes can both characterize different stages during HCC progression and identify cirrhosis as the critical transition stage before carcinogenesis. The interaction effects (i.e. co-expressions) of c</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Aug</publication><modification>2026-05-03T01:15:04.128Z</modification><creation>2019-10-30T08:21:00Z</creation></dates><accession>S-EPMC6788726</accession><cross_references><pubmed>30925583</pubmed><doi>10.1093/jmcb/mjz025</doi></cross_references></HashMap>