Qualitative and quantitative study of dihydrofolate reductase in myelodysplastic syndromes.

Abstract:

:Dihydrofolate reductase (FH2-R) was studied cytochemically in the bone marrow erythroblasts of 20 normal controls and 46 patients with myelodysplastic syndromes (MDSs) classified according to FAB, prior to therapy. The reaction product was quantified for the same samples with a Vickers M86 microdensitometer. The enzyme activity progressively decreased during the normal differentiation of the erythroid cells and persisted at high levels in MDS cells. The high level of FH2-R may be related to the malignant transformation of the cells, or to increased compensatory erythropoietic activity of ineffective erythropoiesis, or to both.

journal_name

Acta Haematol

journal_title

Acta haematologica

authors

Nano R,Invernizzi R,Rezzani R,Gerzeli G

doi

10.1159/000205807

subject

Has Abstract

pub_date

1988-01-01 00:00:00

pages

198-201

issue

4

eissn

0001-5792

issn

1421-9662

journal_volume

79

pub_type

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