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Series GSE162628 Query DataSets for GSE162628
Status Public on Dec 14, 2020
Title Invalidation of a novel marker for therapy-resistant leukemic stem cells responsible for relapse in patients and PDX
Organism Homo sapiens
Experiment type Expression profiling by array
Summary Drug tolerant leukemic cell stem (LSC) subpopulations may explain frequent relapses in acute myeloid leukemia (AML), suggesting that these Relapse-Initiating Cells (RICs) persistent after chemotherapy represent bona fide targets to prevent drug resistance and relapse. We uncover that the G-protein coupled receptor CALCRL is expressed in RICs, and that the overexpression of CALCRL and/or of its ligand adrenomedullin (ADM) and not CGRP correlates to adverse outcome in AML. CALCRL knockdown impairs leukemic growth, decreases LSC frequency and sensitizes to cytarabine in patient-derived xenograft models.
 
Overall design Transfection of MOLM14 cells using genetic approach with shRNA constructs
 
Contributor(s) Kaoma T, Nicot N, Larrue C, Sarry J
Citation(s) 33462236
Submission date Dec 03, 2020
Last update date Feb 01, 2021
Contact name Tony KAOMA
E-mail(s) tony.kaoma@lih.lu
Organization name Luxembourg Institute of Health
Department Quantitative Biology Unit
Lab Bioinfo platform
Street address 1 A-B Rue Thomas Edison
City Strassen
ZIP/Postal code L-1445
Country Luxembourg
 
Platforms (1)
GPL16686 [HuGene-2_0-st] Affymetrix Human Gene 2.0 ST Array [transcript (gene) version]
Samples (8)
GSM4955662 MOLM14 cell transfected with shcontrol rep1
GSM4955663 MOLM14 cell transfected with shcontrol rep2
GSM4955664 MOLM14 cell transfected with shcontrol rep3
Relations
BioProject PRJNA682428

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE162628_RAW.tar 64.1 Mb (http)(custom) TAR (of CEL)
Processed data included within Sample table

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