<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(2)</volume><submitter>Seo SU</submitter><pubmed_abstract>Carboplatin is a less toxic analog of cisplatin, but carboplatin also has side effects, including bone marrow suppression. Therefore, to improve the capacity of the anticancer activity of carboplatin, we investigated whether combined treatment with carboplatin and thioridazine, which has antipsychotic and anticancer activities, has a synergistic effect on apoptosis. Combined treatment with carboplatin and thioridazine markedly induced caspase-mediated apoptosis in head and neck squamous cell carcinoma (AMC-HN4) cells. Combined treatment with carboplatin and thioridazine induced downregulation of Mcl-1 and c-FLIP expression. Ectopic expression of Mcl-1 and c-FLIP inhibited carboplatin plus thioridazine-induced apoptosis. We found that augmentation of proteasome activity had a critical role </pubmed_abstract><journal>Cell death &amp; disease</journal><pagination>e2599</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5386499</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Thioridazine enhances sensitivity to carboplatin in human head and neck cancer cells through downregulation of c-FLIP and Mcl-1 expression.</pubmed_title><pmcid>PMC5386499</pmcid><pubmed_authors>Seo SU</pubmed_authors><pubmed_authors>Park HH</pubmed_authors><pubmed_authors>Woo SM</pubmed_authors><pubmed_authors>Keum YS</pubmed_authors><pubmed_authors>Lee SH</pubmed_authors><pubmed_authors>Kim DE</pubmed_authors><pubmed_authors>Kim S</pubmed_authors><pubmed_authors>Min KJ</pubmed_authors><pubmed_authors>Park JW</pubmed_authors><pubmed_authors>Kim SH</pubmed_authors><pubmed_authors>Choi YH</pubmed_authors><pubmed_authors>Cho HK</pubmed_authors><pubmed_authors>Hyun JW</pubmed_authors><pubmed_authors>Kwon TK</pubmed_authors></additional><is_claimable>false</is_claimable><name>Thioridazine enhances sensitivity to carboplatin in human head and neck cancer cells through downregulation of c-FLIP and Mcl-1 expression.</name><description>Carboplatin is a less toxic analog of cisplatin, but carboplatin also has side effects, including bone marrow suppression. Therefore, to improve the capacity of the anticancer activity of carboplatin, we investigated whether combined treatment with carboplatin and thioridazine, which has antipsychotic and anticancer activities, has a synergistic effect on apoptosis. Combined treatment with carboplatin and thioridazine markedly induced caspase-mediated apoptosis in head and neck squamous cell carcinoma (AMC-HN4) cells. Combined treatment with carboplatin and thioridazine induced downregulation of Mcl-1 and c-FLIP expression. Ectopic expression of Mcl-1 and c-FLIP inhibited carboplatin plus thioridazine-induced apoptosis. We found that augmentation of proteasome activity had a critical role </description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Feb</publication><modification>2025-04-19T19:42:10.264Z</modification><creation>2019-03-27T02:40:53Z</creation></dates><accession>S-EPMC5386499</accession><cross_references><pubmed>28182008</pubmed><doi>10.1038/cddis.2017.8</doi></cross_references></HashMap>