The sequence of application of methotrexate and histone deacetylase inhibitors determines either a synergistic or an antagonistic response in childhood acute lymphoblastic leukemia cells
Author:
Publisher
Springer Science and Business Media LLC
Subject
Oncology,Cancer Research,Hematology
Link
http://www.nature.com/articles/leu2010259.pdf
Reference8 articles.
1. Leclerc GJ, Mou C, Leclerc GM, Mian AM, Barredo JC . Histone deacetylase inhibitors induce FPGS mRNA expression and intracellular accumulation of long-chain methotrexate polyglutamates in childhood acute lymphoblastic leukemia: implications for combination therapy. Leukemia 2010; 24: 552–562.
2. Einsiedel HG, Kawan L, Eckert C, Witt O, Fichtner I, Henze G et al. Histone deacetylase inhibitors have antitumor activity in two NOD/SCID mouse models of B-cell precursor childhood acute lymphoblastic leukemia. Leukemia 2006; 20: 1435–1436.
3. Webb JL . Effect of More than One Inhibitor. Enzymes and Metabolic Inhibitors, vol. 1. Academic Press: New York, 1963, pp 66–79 and 487–512.
4. Kano Y, Akutsu M, Tsunoda S, Izumi T, Kobayashi H, Mano H et al. Cytotoxic effects of histone deacetylase inhibitor FK228 (depsipeptide, formally named FR901228) in combination with conventional anti-leukemia/lymphoma agents against human leukemia/lymphoma cell lines. Invest New Drugs 2007; 25: 31–40.
5. Prasad P, Vasquez H, Das CM, Gopalakrishnan V, Wolff JE . Histone acetylation resulting in resistance to methotrexate in choroid plexus cells. J Neurooncol 2009; 91: 279–286.
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