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Series GSE181006 Query DataSets for GSE181006
Status Public on Mar 24, 2022
Title ZNF521 enhances MLL-AF9-dependent hematopoietic stem cell transformation in acute myeloid leukemias by altering the gene expression landscape
Organism Homo sapiens
Experiment type Expression profiling by array
Summary Leukemias derived from the MLL-AF9 rearrangement rely on deranged transcriptional networks. ZNF521, a transcription co-factor implicated in the control of hematopoiesis, has been proposed to sustain leukemic transformation in collaboration with other oncogenes. We demonstrate here that ZNF521 mRNA levels correlate with specific genetic aberrations: in particular, the highest expression is observed in AMLs bearing MLL rearrangements, while the lowest is detected in AMLs with FLT3-ITD, NPM1 or CEBPα double mutations. In cord blood-derived CD34+ cells, enforced expression of ZNF521 provides a significant proliferative advantage, and acts synergistically when co-expressed with MLL-AF9 throughout the proliferation and expansion of leukemic progenitor cells.
Transcriptome analysis of primary CD34+ cultures displayed subsets of genes upregulated by MLL-AF9 or ZNF521 single transgene overexpression as well as in MLL-AF9/ZNF521 combinations, either at early or late time points of an in vitro model of leukemogenesis. Silencing of ZNF521 in MLL-AF9+ THP-1 cell line coherently results in an impairment of growth and clonogenicity, recapitulating effects observed in primary cells. Taken together, these results underscore a role for ZNF521 in sustaining self-renewal of the AML immature compartment, most likely through the perturbation of the gene expression landscape which ultimately favors the expansion of MLL-AF9 transformed leukemic clones.
 
Overall design Cord blood (CB)-CD34+ cells were trasformed by lentiviral vectors expressing the MLL/AF9 fusion gene (UMG-LV6-MA9) alone or in combination with ZNF521 (UMG-LV6-ZNF521).Global transcript expression profiles of ZNF521, MA9 single transduction conditions were investigated in comparison to control cells at 23 days, whereas ZNF521-MA9 double transduced cells were analyzed both at the 23 and 58 day time points. Duplicate samples were analyzed for each condition.
 
Contributor(s) Chiarella E, Aloisio A, Scicchitano S, Todoerti K, Cosentino EG, Lico D, Neri A, Amodio N, Morrone G, Bond HM, Mesuraca M
Citation(s) 34639154
Submission date Jul 28, 2021
Last update date Mar 25, 2022
Contact name Antonino Neri
E-mail(s) antonino.neri@policlinico.mi.it
Organization name Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico
Lab Hematology
Street address Via Francesco Sforza, 35
City Milan
State/province Milan
ZIP/Postal code 20122
Country Italy
 
Platforms (1)
GPL23126 [Clariom_D_Human] Affymetrix Human Clariom D Assay [transcript (gene) version]
Samples (10)
GSM5481945 Cord blood-CD34+ cells-untreated-replicate 1
GSM5481946 Cord blood-CD34+ cells-untreated-replicate 2
GSM5481947 Cord blood-CD34+ cells-MA9 transduced-at 23 days-replicate 1
Relations
BioProject PRJNA750400

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Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE181006_RAW.tar 242.5 Mb (http)(custom) TAR (of CEL)
Processed data included within Sample table

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