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Series GSE213056 Query DataSets for GSE213056
Status Public on Jan 30, 2023
Title Transcriptomics of AML core bone marrow biopsies reveals distinct therapy response-specific osteo-mesenchymal profiles [microarray]
Organism Homo sapiens
Experiment type Expression profiling by array
Summary While the bone marrow (BM) microenvironment is significantly remodeled in acute myeloid leukemia (AML), our understanding of chemotherapy-induced changes within the BM stroma and their involvement in disease recurrence remains limited. Molecular insight into AML-specific alterations in the microenvironment has been historically limited by the analysis of liquid marrow aspirates rather than core biopsies that contain solid-phase BM stroma with non-hematopoietic cells supporting hematopoiesis. We assessed the effect of standard anthracycline- and cytarabine-based induction chemotherapy on both hematopoietic and non-hematopoietic cells directly in core BM biopsies using RNA-seq and histological analysis to determine the transcriptomic profile and factors associated with the response to treatment. We compared matched human core BM biopsies at diagnosis and 2 weeks after standard cytarabine/anthracycline induction therapy in responders (<5% blasts present post-treatment ) and non-responders (>5% blasts present post-treatment). Our data indicated enrichment in vimentin (VIM), platelet-derived growth factor receptor beta (PDGFRB) and Snail family transcriptional repressor 2(SNAI2) transcripts in responders, consistent with the reactivation of the mesenchymal population in the BM stroma. Enrichment of osteoblast maturation-related transcripts of biglycan (BGN), osteopontin (SPP1), and osteonectin (SPARC) was observed in core BM biopsies from non-responders to induction chemotherapy. To the best of our knowledge, this is the first report demonstrating distinct osteogenic and mesenchymal transcriptome profiles specific to AML BM response to induction chemotherapy assessed directly in core BM biopsies. Detailing treatment response-specific alterations in the BM stroma may inform optimized therapeutic strategies for AML.
 
Overall design Comparative gene expression profiling analysis of responders and non-responders to standard induction therapy in AML. Total mRNA was extracted from paired FFPE core bone marrow biopsies obtained at diagnosis (responder n=6/nonresponder n=5) and 2-weeks post-treatment (responder n=6/nonresponder n=5) induction.
 
Contributor(s) Treaba DO, Bonal DM, Castillo-Martin M, Chorzalska A, Oakes A, Pardo M, Petersen M, Schorl C, Hopkins K, Melcher D, Zhao TC, Liang O, So E, Reagan J, Olszewski AJ, Butera J, Anthony DC, Rintels P, Quesenberry P, Dubielecka PM
Citation(s) 36354085
Submission date Sep 09, 2022
Last update date Jan 31, 2023
Contact name Patrycja M Dubielecka
E-mail(s) patrycja_dubielecka-szczerba@brown.edu
Organization name Warren Alpert Medical School of Brown University and Rhode Island Hospital
Department Division of Hematology/Oncology, Department of Medicine
Lab Dubielecka Lab
Street address 1 Hoppin St., Coro West, 5th Fl., Suite 5.36
City Providence
State/province RI
ZIP/Postal code 02903
Country USA
 
Platforms (1)
GPL23126 [Clariom_D_Human] Affymetrix Human Clariom D Assay [transcript (gene) version]
Samples (22)
GSM6570825 FFPE bone marrow, Responder Post-Treatment, biological rep2
GSM6570826 FFPE bone marrow, Responder Post-Treatment, biological rep4
GSM6570827 FFPE bone marrow, Responder Post-Treatment, biological rep1
This SubSeries is part of SuperSeries:
GSE213210 Transcriptomics of AML core bone marrow biopsies reveals distinct therapy response-specific osteo-mesenchymal profiles by RNA-seq and microarray analysis
Relations
BioProject PRJNA878839

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Supplementary file Size Download File type/resource
GSE213056_RAW.tar 491.6 Mb (http)(custom) TAR (of CEL)
Processed data included within Sample table

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