<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lane SW</submitter><funding>NIDDK NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>NCI NIH HHS</funding><pagination>2849-56</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3172801</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>118(10)</volume><pubmed_abstract>Hematopoietic stem cells (HSCs) engage in complex bidirectional signals with the hematopoietic microenvironment (HM), and there is emerging evidence that leukemia stem cells (LSCs) may use similar interactions. Using a syngeneic retroviral model of MLL-AF9 induced acute myeloid leukemia (AML), we have identified 2 different stages of leukemia progression, propagated by "pre-LSCs" and established leukemia (LSCs) and compared the homing properties of these distinctive entities to that of normal HSCs. The homing and microlocalization of pre-LSCs was most similar to long-term HSCs and was dependent on cell-intrinsic Wnt signaling. In contrast, the homing of established LSCs was most similar to that of committed myeloid progenitors and distinct from HSCs. Although osteoblast-derived Dickkopf-1,</pubmed_abstract><journal>Blood</journal><pubmed_title>Differential niche and Wnt requirements during acute myeloid leukemia progression.</pubmed_title><pmcid>PMC3172801</pmcid><funding_grant_id>R01 DK062757</funding_grant_id><funding_grant_id>P01 CA066996</funding_grant_id><funding_grant_id>R01 HL044851</funding_grant_id><funding_grant_id>DK62757</funding_grant_id><funding_grant_id>HL44851</funding_grant_id><funding_grant_id>CA66996</funding_grant_id><pubmed_authors>Lane SW</pubmed_authors><pubmed_authors>Sykes SM</pubmed_authors><pubmed_authors>Bullinger L</pubmed_authors><pubmed_authors>Ferraro F</pubmed_authors><pubmed_authors>Lo Celso C</pubmed_authors><pubmed_authors>Wang YJ</pubmed_authors><pubmed_authors>Armstrong SA</pubmed_authors><pubmed_authors>Williams DA</pubmed_authors><pubmed_authors>Ragu C</pubmed_authors><pubmed_authors>Shterental S</pubmed_authors><pubmed_authors>Lin CP</pubmed_authors><pubmed_authors>Scadden DT</pubmed_authors><pubmed_authors>Gilliland DG</pubmed_authors></additional><is_claimable>false</is_claimable><name>Differential niche and Wnt requirements during acute myeloid leukemia progression.</name><description>Hematopoietic stem cells (HSCs) engage in complex bidirectional signals with the hematopoietic microenvironment (HM), and there is emerging evidence that leukemia stem cells (LSCs) may use similar interactions. Using a syngeneic retroviral model of MLL-AF9 induced acute myeloid leukemia (AML), we have identified 2 different stages of leukemia progression, propagated by "pre-LSCs" and established leukemia (LSCs) and compared the homing properties of these distinctive entities to that of normal HSCs. The homing and microlocalization of pre-LSCs was most similar to long-term HSCs and was dependent on cell-intrinsic Wnt signaling. In contrast, the homing of established LSCs was most similar to that of committed myeloid progenitors and distinct from HSCs. Although osteoblast-derived Dickkopf-1,</description><dates><release>2011-01-01T00:00:00Z</release><publication>2011 Sep</publication><modification>2025-07-02T03:04:57.89Z</modification><creation>2025-07-02T03:04:57.89Z</creation></dates><accession>S-EPMC3172801</accession><cross_references><pubmed>21765021</pubmed><doi>10.1182/blood-2011-03-345165</doi></cross_references></HashMap>