<HashMap><database>ENA</database><scores/><additional><omics_type>Genomics</omics_type><center_name>Weinstock Lab, Medical Oncology, Dana-Farber Cancer Institute</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA261873</full_dataset_link><scientific_name>Homo sapiens</scientific_name><long_description>Gene expression profiling was performed to define transcriptional programs associated with response to type II JAK2 inhibitor NVP-CHZ868 alone or in combination with dexamethasone in vitro and in vivo. Overall design: MHH-CALL4 cells harboring a CRLF2 rearrangement and JAK2 I682F mutation were treated with vehicle, CHZ868, dexamethasone, or CHZ868 + dexamethasone combination for 12 hours in triplicate. RNA was then extracted for hybridization on Affymetrix microarrays. CRLF2+ patient-derived xenografts (05-412, 05-440, and 05-537) were treated in vivo for 3 days with vehicle, CHZ868, dexamethasone, or CHZ868 + dexmathasone combination for 3 days and then sacrificed. Transcriptional profiling was performed on unselected splenocytes from these animals.</long_description><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>Homo sapiens</name><description>Type II JAK2 Inhibitor NVP-CHZ868 is Active in Vitro and in Vivo Against JAK2-Dependent B-cell Acute Lymphoblastic Leukemias</description><dates><last_updated>2025-09-24</last_updated><first_public>2015-06-20</first_public></dates><accession>PRJNA261873</accession><cross_references><GEO>GSE61696</GEO><taxon>9606</taxon></cross_references></HashMap>