<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Valdez BC</submitter><pubmed_abstract>The antineoplastic activity of pre-transplant regimens in hematopoietic stem cell transplantation (HSCT) is a critical factor for acute myeloid leukemia (AML) patients. There is an urgent need to identify novel approaches without jeopardizing patient safety. We hypothesized that combination of drugs with different mechanisms of action would provide better cytotoxicity. We, therefore, determined the synergistic cytotoxicity of various combinations of the alkylating agents busulfan (Bu) and 4-hydroperoxycyclophosphamide (4HC), the nucleoside analog fludarabine (Flu) and the BCL2 inhibitor ABT199/venetoclax in AML cells. [Bu+4HC] and [Bu+Flu] inhibited cell proliferation and activated apoptosis; addition of ABT199 to either combinations significantly increased these effects with combination i</pubmed_abstract><journal>Oncotarget</journal><pagination>319-330</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8830224</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>ABT199/venetoclax potentiates the cytotoxicity of alkylating agents and fludarabine in acute myeloid leukemia cells.</pubmed_title><pmcid>PMC8830224</pmcid><pubmed_authors>Andersson BS</pubmed_authors><pubmed_authors>Murray D</pubmed_authors><pubmed_authors>Valdez BC</pubmed_authors><pubmed_authors>Yuan B</pubmed_authors><pubmed_authors>Nieto Y</pubmed_authors><pubmed_authors>Popat U</pubmed_authors></additional><is_claimable>false</is_claimable><name>ABT199/venetoclax potentiates the cytotoxicity of alkylating agents and fludarabine in acute myeloid leukemia cells.</name><description>The antineoplastic activity of pre-transplant regimens in hematopoietic stem cell transplantation (HSCT) is a critical factor for acute myeloid leukemia (AML) patients. There is an urgent need to identify novel approaches without jeopardizing patient safety. We hypothesized that combination of drugs with different mechanisms of action would provide better cytotoxicity. We, therefore, determined the synergistic cytotoxicity of various combinations of the alkylating agents busulfan (Bu) and 4-hydroperoxycyclophosphamide (4HC), the nucleoside analog fludarabine (Flu) and the BCL2 inhibitor ABT199/venetoclax in AML cells. [Bu+4HC] and [Bu+Flu] inhibited cell proliferation and activated apoptosis; addition of ABT199 to either combinations significantly increased these effects with combination i</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-21T23:14:41.513Z</modification><creation>2025-04-05T19:04:54.769Z</creation></dates><accession>S-EPMC8830224</accession><cross_references><pubmed>35154579</pubmed><doi>10.18632/oncotarget.28193</doi></cross_references></HashMap>