<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Patel SB</submitter><funding>NIAID NIH HHS</funding><funding>NHLBI NIH HHS</funding><pagination>1-13</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12087282</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>115</volume><pubmed_abstract>Despite decades of research, standard therapies remain ineffective for most leukemias, pushing toward an essential unmet need for targeted drug screens. Moreover, preclinical drug testing is an important consideration for success of clinical trials without affecting non-transformed stem cells. Using the transgenic chronic myeloid leukemia (CML) mouse model, we determine that leukemic stem cells (LSCs) are transcriptionally heterogenous with a preexistent drug-insensitive signature. To test targeting of potentially important pathways, we establish ex vivo expanded LSCs that have long-term engraftment and give rise to multilineage hematopoiesis. Expanded LSCs share transcriptomic signatures with primary LSCs including enrichment in Wnt, JAK-STAT, MAPK, mTOR and transforming growth factor β s</pubmed_abstract><journal>Experimental hematology</journal><pubmed_title>Ex Vivo Expansion of Phenotypic and Transcriptomic Chronic Myeloid Leukemia Stem Cells.</pubmed_title><pmcid>PMC12087282</pmcid><funding_grant_id>P30 AI027767</funding_grant_id><funding_grant_id>R01 HL150078</funding_grant_id><funding_grant_id>P01 HL131477</funding_grant_id><pubmed_authors>Bassal MA</pubmed_authors><pubmed_authors>Welner RS</pubmed_authors><pubmed_authors>Franceski AM</pubmed_authors><pubmed_authors>Patel SB</pubmed_authors><pubmed_authors>Kuznetsova V</pubmed_authors><pubmed_authors>Matkins VR</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ex Vivo Expansion of Phenotypic and Transcriptomic Chronic Myeloid Leukemia Stem Cells.</name><description>Despite decades of research, standard therapies remain ineffective for most leukemias, pushing toward an essential unmet need for targeted drug screens. Moreover, preclinical drug testing is an important consideration for success of clinical trials without affecting non-transformed stem cells. Using the transgenic chronic myeloid leukemia (CML) mouse model, we determine that leukemic stem cells (LSCs) are transcriptionally heterogenous with a preexistent drug-insensitive signature. To test targeting of potentially important pathways, we establish ex vivo expanded LSCs that have long-term engraftment and give rise to multilineage hematopoiesis. Expanded LSCs share transcriptomic signatures with primary LSCs including enrichment in Wnt, JAK-STAT, MAPK, mTOR and transforming growth factor β s</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2026-06-01T05:16:44.027Z</modification><creation>2026-04-08T09:31:00.009Z</creation></dates><accession>S-EPMC12087282</accession><cross_references><pubmed>36115580</pubmed><doi>10.1016/j.exphem.2022.09.001</doi></cross_references></HashMap>