<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10(8)</volume><submitter>Liu XC</submitter><pubmed_abstract>Multidrug resistance-associated protein 2 (MRP2) plays an important role in bile acid metabolism by transporting toxic organic anion conjugates, including conjugated bilirubin, glutathione, sulfate, and multifarious drugs. MRP2 expression is reduced in cholestatic patients and rodents. However, the molecular mechanism of MRP2 down-regulation remains elusive. In this report, we treated human hepatoma HepG2 cells with interleukin-18 (IL-18) and measured the expression of MRP2, nuclear factor kappa B (NF-κB), farnesoid X receptor (FXR), and the transcription factor Yin Yang 1 (YY1) by quantitative real-time quantitative polymerase chain reaction (PCR) and western blotting. We found that expression of MRP2 was repressed by IL-18 at both the mRNA and protein levels in a dose- and time-dependent</pubmed_abstract><journal>PloS one</journal><pagination>e0136215</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4546195</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Interleukin-18 Down-Regulates Multidrug Resistance-Associated Protein 2 Expression through Farnesoid X Receptor Associated with Nuclear Factor Kappa B and Yin Yang 1 in Human Hepatoma HepG2 Cells.</pubmed_title><pmcid>PMC4546195</pmcid><pubmed_authors>Lian W</pubmed_authors><pubmed_authors>Yang L</pubmed_authors><pubmed_authors>Zhang LJ</pubmed_authors><pubmed_authors>Chen L</pubmed_authors><pubmed_authors>Chai J</pubmed_authors><pubmed_authors>Cheng Y</pubmed_authors><pubmed_authors>Wang XJ</pubmed_authors><pubmed_authors>Chen WS</pubmed_authors><pubmed_authors>Li SX</pubmed_authors><pubmed_authors>Feng XC</pubmed_authors><pubmed_authors>Gao Y</pubmed_authors><pubmed_authors>Liu C</pubmed_authors><pubmed_authors>Wang RQ</pubmed_authors><pubmed_authors>Liu XC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Interleukin-18 Down-Regulates Multidrug Resistance-Associated Protein 2 Expression through Farnesoid X Receptor Associated with Nuclear Factor Kappa B and Yin Yang 1 in Human Hepatoma HepG2 Cells.</name><description>Multidrug resistance-associated protein 2 (MRP2) plays an important role in bile acid metabolism by transporting toxic organic anion conjugates, including conjugated bilirubin, glutathione, sulfate, and multifarious drugs. MRP2 expression is reduced in cholestatic patients and rodents. However, the molecular mechanism of MRP2 down-regulation remains elusive. In this report, we treated human hepatoma HepG2 cells with interleukin-18 (IL-18) and measured the expression of MRP2, nuclear factor kappa B (NF-κB), farnesoid X receptor (FXR), and the transcription factor Yin Yang 1 (YY1) by quantitative real-time quantitative polymerase chain reaction (PCR) and western blotting. We found that expression of MRP2 was repressed by IL-18 at both the mRNA and protein levels in a dose- and time-dependent</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015</publication><modification>2025-04-04T12:39:15.812Z</modification><creation>2019-03-26T22:55:57Z</creation></dates><accession>S-EPMC4546195</accession><cross_references><pubmed>26292095</pubmed><doi>10.1371/journal.pone.0136215</doi></cross_references></HashMap>