Volume 105, Issue 2 pp. 448-451

Clofibric acid: a potential therapeutic agent in AML and MDS

S. L. Fenton

S. L. Fenton

Departments of Medicine,

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M. T. Drayson

M. T. Drayson

Immunology, University of Birmingham Medical School, Edgbaston, Birmingham, (

LRF Differentiation Programme)

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M. Hewison

M. Hewison

Departments of Medicine,

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E. Vickers

E. Vickers

Departments of Medicine,

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G. Brown

G. Brown

Immunology, University of Birmingham Medical School, Edgbaston, Birmingham, (

LRF Differentiation Programme)

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C. M. Bunce

C. M. Bunce

LRF Differentiation Programme)

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First published: 17 February 2005
Citations: 9
Dr C. M. Bunce Department of Medicine, University of Birmingham, Birmingham B15 2TH. e-mail: c.m.bunce@bham. ac.uk

Abstract

Differentiation therapy using retinoic acids (RAs) or 1α25-dihydroxyvitamin D3 (D3) is an attractive alternative to chemotherapy in acute myeloid leukaemia (AML) and myelodysplastic syndromes (MDS). However, with the exception of RA therapy for acute promyelocytic leukaemia (APL), RAs and D3 are not potent enough at doses that can be tolerated by patients. We demonstrate that clofibric acid (CA) enhances the response of HL60 cells to all-trans RA and D3. Our findings and those of others in the field lead us to suggest that combination therapy using all-trans RA and CA should be considered as potential therapy for AML and MDS.

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