Potential mechanisms of resistance to cytarabine in AML patients

被引:119
作者
Galmarini, CM
Thomas, X
Calvo, F
Rousselot, P
El Jafaari, A
Cros, E
Dumontet, C
机构
[1] Fac Med Rockefeller, Unite 453, INSERM, Lab Cytol Analyt, F-69373 Lyon 08, France
[2] Hop Edouard Herriot, Serv Hematol, Lyon, France
[3] Hop St Louis, Pharmacol Lab, AP HP, INSERM,CIC 9504, Paris, France
[4] Hop St Louis, Pharmacol Lab, EP9932, INSERM,CIC 9504, Paris, France
[5] Hop St Louis, Serv Hematol, Paris, France
[6] Hop Edouard Herriot, Ctr Transfus, Lyon, France
关键词
drug resistance; cytarabine; 5 '-nucleotidase; acute myeloid leukemia; antineoplastic agents; antimetabolites;
D O I
10.1016/S0145-2126(01)00184-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
To determine whether the human equilibrative nucleoside transporter 1 (hENT 1), deoxycytidine kinase(dCK), cytoplasmic 5'-nucleotidase (5NT), cytidine deaminase (CDD), topoisomerase 1 (TOPO 1) and topoisomerase 11 alpha (TOPO 11) are involved in clinical resistance to cytarabine (ara-C), we analyzed the level of expression of these parameters by reverse transcriptase polymerase chain reaction (rt-PCR), at diagnosis in the blast cells of 77 acute myeloid leukemia (AML) patients treated with ara-C, including 3 1 for whom samples were collected at first relapse. By univariate and/or multivariate analyses, patients with expression of 5NT or hENT1 deficiency at diagnosis had significantly shorter disease-free survival (DFS) and overall survival (OS). These results suggest that expression of 5NT and reduced hENT1 in leukemic blasts at diagnosis are correlated with clinical outcome and may play a role in resistance mechanisms to ara-C in patients with AML. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:621 / 629
页数:9
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