Gene expression profiling of leukemia T-cells resistant to methotrexate and 7-hydroxymethotrexate reveals alterations that preserve intracellular levels of folate and nucleotide biosynthesis

被引:25
作者
Fotoohi, Alan Kambiz [1 ]
Assaraf, Yehuda G. [2 ]
Moshfegh, Ali [1 ]
Hashemi, Jamileh [3 ]
Jansen, Gerrit [4 ]
Peters, Godefridus J. [4 ]
Larsson, Catharina [3 ]
Albertioni, Freidoun [1 ]
机构
[1] Karolinska Univ Hosp, Dept Pathol & Oncol, Karolinska Inst, Canc Ctr Karolinska, SE-17176 Stockholm, Sweden
[2] Technion Israel Inst Technol, Dept Biol, Fred Wyszkowski Canc Res Lab, IL-32000 Haifa, Israel
[3] CMM Karolinska Univ Hosp, Karolinska Inst, Dept Mol Med & Surg, Stockholm, Sweden
[4] Vrije Univ Amsterdam, Med Ctr, Dept Med Oncol, Amsterdam, Netherlands
关键词
Methotrexate; 7-Hydroxymethotrexate; Resistance; Leukemia; Folylpolyglutamate synthetase; Reduced folate carrier; Thymidylate synthase; Microarray; Real-time quantitative RT-PCR; ACUTE LYMPHOBLASTIC-LEUKEMIA; ANTIFOLATE RESISTANCE; PROTEIN BCRP/ABCG2; TRANSCRIPTION FACTORS; CARRIER GENE; MECHANISM; TRANSPORT; METABOLITES; MULTIPLE; EFFICACY;
D O I
10.1016/j.bcp.2008.12.026
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In vitro treatment of human T-cell leukemia cells with 7-hydroxymethotrexate, the major metabolite of methotrexate resulted in acquired resistance is a result of the complete loss of folypolyglutamate synthetase (FPGS) activity. This was in contradistinction to the major modality of antifolate resistance of impaired drug transport in leukemia cells exposed to methotrexate. To identify the genes associated with methotrexate and 7-hydroxymethotrexate resistance, we herein explored the patterns of genome-wide expression profiles in these antifolte-resistant leukemia sublines. mRNA levels of the reduced folate carrier, the primary influx transporter of folates and antifolates, were down-regulated more than two-fold in methotrexate-resistant cells. The dramatic loss of FPGS activity in 7-hydroxymethotrexate-resistant cells was associated with alterations in the expression of various genes aimed at preserving reduced folates and/or enhancing purine nucleotide biosynthesis, e.g.. methylene tetrahydrofolate reductase, glycinamide ribonucleotide formyltransferase, adenosine deaminase, cystathionine beta synthase, as well as the ATP-dependent folate exporters BCRP/ABCG2 and MRPI/ABCC1. The observed changes in gene expression were generally not paralleled by acquired DNA Copy numbers alterations, suggesting transcriptional regulatory mechanisms. Interestingly, gene expression of DNA/RNA metabolism and transport genes were more profoundly altered in methotrexate-resistant subline, whereas in 7-hydroxymethotrexate-resistant cells, tire most profoundly affected groups of genes were those encoding for proteins involved in metabolism and cellular proliferation. Thus, the present investigation provides evidence that 7-hydroxymethotrexate induces gene expression alterations and an antifolate resistance modality that are distinct from its parent drug methotrexate. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:1410 / 1417
页数:8
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