<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Han W</submitter><funding>NIDDK NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>NCI NIH HHS</funding><pubmed_abstract>Hematopoietic stem cell transplantation is a common treatment for many blood disorders and can be a life-saving therapy for patients with leukemias, lymphomas and multiple myeloma. Umbilical cord blood (UCB) serves as a valuable source of hematopoietic stem and progenitor cells (HSPCs) for transplantation, particularly for patients lacking a matched donor. However, the limited number of repopulating cells in UCB units restricts its clinical utility. Our prior studies showed that genetic deletion of the polycomb repressive complex 2 (PRC2) co-factor &lt;i>Jarid2&lt;/i> in mouse multipotent progenitors (MPPs) conveyed ectopic self-renewal capacity. Here, we hypothesized that the function of human HSPCs could be enhanced through &lt;i>JARID2&lt;/i> inhibition. In this study, we demonstrate that both cons</pubmed_abstract><journal>bioRxiv : the preprint server for biology</journal><pagination>2025.09.03.672211</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12424646</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>JARID2 Inhibition Reprograms Human Hematopoietic Progenitor Cells To Enhance Bone Marrow Transplantation.</pubmed_title><pmcid>PMC12424646</pmcid><funding_grant_id>R01 HL147978</funding_grant_id><funding_grant_id>K99 HL165103</funding_grant_id><funding_grant_id>P30 CA091842</funding_grant_id><funding_grant_id>K99 CA296777</funding_grant_id><funding_grant_id>R01 DK119231</funding_grant_id><funding_grant_id>R01 DK124883</funding_grant_id><funding_grant_id>T32 HL007088</funding_grant_id><funding_grant_id>R01 HL152180</funding_grant_id><pubmed_authors>Raj IX</pubmed_authors><pubmed_authors>Burkart SC</pubmed_authors><pubmed_authors>Rettig M</pubmed_authors><pubmed_authors>Han W</pubmed_authors><pubmed_authors>Celik H</pubmed_authors><pubmed_authors>Challen GA</pubmed_authors><pubmed_authors>Yang W</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Young AL</pubmed_authors><pubmed_authors>Magee JA</pubmed_authors><pubmed_authors>Zhang CR</pubmed_authors><pubmed_authors>Parsons TM</pubmed_authors><pubmed_authors>Arand J</pubmed_authors><pubmed_authors>Issa N</pubmed_authors><pubmed_authors>Bjeije H</pubmed_authors><pubmed_authors>Krishnan A</pubmed_authors></additional><is_claimable>false</is_claimable><name>JARID2 Inhibition Reprograms Human Hematopoietic Progenitor Cells To Enhance Bone Marrow Transplantation.</name><description>Hematopoietic stem cell transplantation is a common treatment for many blood disorders and can be a life-saving therapy for patients with leukemias, lymphomas and multiple myeloma. Umbilical cord blood (UCB) serves as a valuable source of hematopoietic stem and progenitor cells (HSPCs) for transplantation, particularly for patients lacking a matched donor. However, the limited number of repopulating cells in UCB units restricts its clinical utility. Our prior studies showed that genetic deletion of the polycomb repressive complex 2 (PRC2) co-factor &lt;i>Jarid2&lt;/i> in mouse multipotent progenitors (MPPs) conveyed ectopic self-renewal capacity. Here, we hypothesized that the function of human HSPCs could be enhanced through &lt;i>JARID2&lt;/i> inhibition. In this study, we demonstrate that both cons</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-04-29T03:22:09.654Z</modification><creation>2026-04-29T03:13:11.143Z</creation></dates><accession>S-EPMC12424646</accession><cross_references><pubmed>40950155</pubmed><doi>10.1101/2025.09.03.672211</doi></cross_references></HashMap>