<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ibrahim SL</submitter><funding>Iraqi Cultural Attaché in London (Iraqi Cultural Attaché - London)</funding><funding>North Staffordshire medical institute, Staffordshire No grant reference number.</funding><funding>Iraqi Cultural Attaché in London</funding><funding>Higher Committee for Education Development in Iraq (HCED)</funding><funding>Higher Committee for Education Development in Iraq</funding><pagination>896-906</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9977917</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>128(5)</volume><pubmed_abstract>&lt;h4>Context&lt;/h4>Many cancer patients who initially respond to chemotherapy eventually develop chemoresistance, and to address this, we previously conducted a RNAi screen to identify genes contributing to resistance. One of the hits from the screen was branched-chain α-keto acid dehydrogenase kinase (BCKDK). BCKDK controls the metabolism of branched-chain amino acids (BCAAs) through phosphorylation and inactivation of the branched-chain α-keto acid dehydrogenase complex (BCKDH), thereby inhibiting catabolism of BCAAs.&lt;h4>Methods&lt;/h4>We measured the impact on paclitaxel sensitivity of inhibiting BCKDK in ovarian and breast cancer cell lines.&lt;h4>Results&lt;/h4>Inhibition of BCKDK using siRNA or two chemical inhibitors (BCKDKi) was synergistic with paclitaxel in both breast and ovarian cancer cel</pubmed_abstract><journal>British journal of cancer</journal><pubmed_title>Inhibition of branched-chain alpha-keto acid dehydrogenase kinase augments the sensitivity of ovarian and breast cancer cells to paclitaxel.</pubmed_title><pmcid>PMC9977917</pmcid><funding_grant_id>D-11-296</funding_grant_id><funding_grant_id>S939</funding_grant_id><funding_grant_id>S1442</funding_grant_id><pubmed_authors>Richardson A</pubmed_authors><pubmed_authors>Ibrahim SL</pubmed_authors><pubmed_authors>Price JC</pubmed_authors><pubmed_authors>Abdullah MI</pubmed_authors><pubmed_authors>Abed MN</pubmed_authors><pubmed_authors>Mohamed G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Inhibition of branched-chain alpha-keto acid dehydrogenase kinase augments the sensitivity of ovarian and breast cancer cells to paclitaxel.</name><description>&lt;h4>Context&lt;/h4>Many cancer patients who initially respond to chemotherapy eventually develop chemoresistance, and to address this, we previously conducted a RNAi screen to identify genes contributing to resistance. One of the hits from the screen was branched-chain α-keto acid dehydrogenase kinase (BCKDK). BCKDK controls the metabolism of branched-chain amino acids (BCAAs) through phosphorylation and inactivation of the branched-chain α-keto acid dehydrogenase complex (BCKDH), thereby inhibiting catabolism of BCAAs.&lt;h4>Methods&lt;/h4>We measured the impact on paclitaxel sensitivity of inhibiting BCKDK in ovarian and breast cancer cell lines.&lt;h4>Results&lt;/h4>Inhibition of BCKDK using siRNA or two chemical inhibitors (BCKDKi) was synergistic with paclitaxel in both breast and ovarian cancer cel</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Mar</publication><modification>2025-04-18T14:13:24.765Z</modification><creation>2025-04-07T00:15:00.574Z</creation></dates><accession>S-EPMC9977917</accession><cross_references><pubmed>36526674</pubmed><doi>10.1038/s41416-022-02095-9</doi></cross_references></HashMap>