<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>49(3)</volume><submitter>Sun L</submitter><pubmed_abstract>Sorafenib is a targeted drug for hepatocellular carcinoma (HCC), however, its efficacy is limited. Nuclear factor erythroid 2‑related factor 2 (Nrf2) contributes to sorafenib resistance. The present study investigated camptothecin (CPT) as a Nrf2 inhibitor to sensitize HCC to sorafenib. The effect of CPT on sorafenib sensitivity in HCC was assessed &lt;i>in vivo&lt;/i> using H22 mice model (n=32) and VX2 rabbit models (n=32), which were sorted into four treatment groups. The expression levels of Nrf2, its downstream genes, including heme oxygenases‑1 (HO‑1) and NAD(P)H quinone oxidoreductase 1 (NQO1), and the epithelial‑mesenchymal transition markers Snail and N‑cadherin in tumors were determined using immunohistochemical staining and western blotting. Magnetic resonance imaging was used to moni</pubmed_abstract><journal>Oncology reports</journal><pagination>55</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9926516</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Camptothecin improves sorafenib sensitivity by inhibiting Nrf2‑ARE pathway in hepatocellular carcinoma.</pubmed_title><pmcid>PMC9926516</pmcid><pubmed_authors>Sun L</pubmed_authors><pubmed_authors>Meng F</pubmed_authors><pubmed_authors>Li G</pubmed_authors><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Liu Q</pubmed_authors><pubmed_authors>Chen F</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Chang S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Camptothecin improves sorafenib sensitivity by inhibiting Nrf2‑ARE pathway in hepatocellular carcinoma.</name><description>Sorafenib is a targeted drug for hepatocellular carcinoma (HCC), however, its efficacy is limited. Nuclear factor erythroid 2‑related factor 2 (Nrf2) contributes to sorafenib resistance. The present study investigated camptothecin (CPT) as a Nrf2 inhibitor to sensitize HCC to sorafenib. The effect of CPT on sorafenib sensitivity in HCC was assessed &lt;i>in vivo&lt;/i> using H22 mice model (n=32) and VX2 rabbit models (n=32), which were sorted into four treatment groups. The expression levels of Nrf2, its downstream genes, including heme oxygenases‑1 (HO‑1) and NAD(P)H quinone oxidoreductase 1 (NQO1), and the epithelial‑mesenchymal transition markers Snail and N‑cadherin in tumors were determined using immunohistochemical staining and western blotting. Magnetic resonance imaging was used to moni</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Mar</publication><modification>2025-04-04T12:42:16.988Z</modification><creation>2025-04-04T12:42:16.988Z</creation></dates><accession>S-EPMC9926516</accession><cross_references><pubmed>36734286</pubmed><doi>10.3892/or.2023.8492</doi></cross_references></HashMap>