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Flow cytometry of DNMT1 as a biomarker of hypomethylating therapies.

Authors :
Woost PG
William BM
Cooper BW
Ueda Oshima M
Otegbeye F
De Lima MJ
Wald D
Mahfouz RZ
Saunthararajah Y
Stefan T
Jacobberger JW
Source :
Cytometry. Part B, Clinical cytometry [Cytometry B Clin Cytom] 2024 Jan; Vol. 106 (1), pp. 11-24. Date of Electronic Publication: 2024 Feb 12.
Publication Year :
2024

Abstract

The 5-azacytidine (AZA) and decitabine (DEC) are noncytotoxic, differentiation-inducing therapies approved for treatment of myelodysplastic syndrome, acute myeloid leukemias (AML), and under evaluation as maintenance therapy for AML postallogeneic hematopoietic stem cell transplant and to treat hemoglobinapathies. Malignant cell cytoreduction is thought to occur by S-phase specific depletion of the key epigenetic regulator, DNA methyltransferase 1 (DNMT1) that, in the case of cancers, thereby releases terminal-differentiation programs. DNMT1-targeting can also elevate expression of immune function genes (HLA-DR, MICA, MICB) to stimulate graft versus leukemia effects. In vivo, there is a large inter-individual variability in DEC and 5-AZA activity because of pharmacogenetic factors, and an assay to quantify the molecular pharmacodynamic effect of DNMT1-depletion is a logical step toward individualized or personalized therapy. We developed and analytically validated a flow cytometric assay for DNMT1 epitope levels in blood and bone marrow cell subpopulations defined by immunophenotype and cell cycle state. Wild type (WT) and DNMT1 knock out (DKO) HC116 cells were used to select and optimize a highly specific DNMT1 monoclonal antibody. Methodologic validation of the assay consisted of cytometry and matching immunoblots of HC116-WT and -DKO cells and peripheral blood mononuclear cells; flow cytometry of H116-WT treated with DEC, and patient samples before and after treatment with 5-AZA. Analysis of patient samples demonstrated assay reproducibility, variation in patient DNMT1 levels prior to treatment, and DNMT1 depletion posttherapy. A flow-cytometry assay has been developed that in the research setting of clinical trials can inform studies of DEC or 5-AZA treatment to achieve targeted molecular pharmacodynamic effects and better understand treatment-resistance/failure.<br /> (© 2024 The Authors. Cytometry Part B: Clinical Cytometry published by Wiley Periodicals LLC on behalf of International Clinical Cytometry Society.)

Details

Language :
English
ISSN :
1552-4957
Volume :
106
Issue :
1
Database :
MEDLINE
Journal :
Cytometry. Part B, Clinical cytometry
Publication Type :
Academic Journal
Accession number :
38345160
Full Text :
https://doi.org/10.1002/cyto.b.22158