Mechanisms of antifolate resistance and methotrexate efficacy in leukemia cells

被引:78
作者
Fotoohi, Alan Kambiz [1 ]
Albertioni, Freidoun [1 ]
机构
[1] Karolinska Hosp, CCK, Dept Pathol & Oncol, S-17176 Stockholm, Sweden
关键词
leukemia; methotrexate; 7-hydroxymethotrexate; resistance; transport;
D O I
10.1080/10428190701824569
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Antifolates are the first class of antimetabolites introduced to clinic about 6 decades ago. Now, after several years of administration of antifolates against malignancies and particularly leukemia, we are still trying to achieve a full understanding of the mechanisms of action and resistance to these agents. The present article covers different factors able to influence efficacy of antifolates on leukemic cells, the known mechanisms of resistance to methotrexate (MTX) and strategies to overcome these mechanisms. The dominant factors that are contributed to tolerance to cytocidal effects of MTX including pharmacokinetic factors, impaired transmembrane uptake as the most frequent rote of provoking resistance to MTX, augmented drug efflux, impaired intracellular polyglutamation as a determining process of drug efficacy, alterations in expression or activity of target enzymes and increased intracellular folate pools; and finally role of 7-hydroxymethotrexate on response or resistance to MTX will be discussed in more detail. Finally, strategies to overcome resistance to antifolates are discussed.
引用
收藏
页码:410 / 426
页数:17
相关论文
共 161 条
[1]   LST-2, a human liver-specific organic anion transporter, determines methotrexate sensitivity in gastrointestinal cancers [J].
Abe, T ;
Unno, M ;
Onogawa, T ;
Tokui, T ;
Kondo, TN ;
Nakagomi, R ;
Adachi, H ;
Fujiwara, K ;
Okabe, M ;
Suzuki, T ;
Nunoki, K ;
Sato, E ;
Kakyo, M ;
Nishio, T ;
Sugita, J ;
Asano, N ;
Tanemoto, M ;
Seki, M ;
Date, F ;
Ono, K ;
Kondo, Y ;
Shiiba, K ;
Suzuki, M ;
Ohtani, H ;
Shimosegawa, T ;
Iinuma, K ;
Nagura, H ;
Ito, S ;
Matsuno, S .
GASTROENTEROLOGY, 2001, 120 (07) :1689-1699
[2]  
Albertioni F, 1996, CLIN CHEM, V42, P39
[3]  
ALLEGRA CJ, 1987, J BIOL CHEM, V262, P13520
[4]  
ALT FW, 1978, J BIOL CHEM, V253, P1357
[5]  
ALT FW, 1976, J BIOL CHEM, V251, P3063
[6]   SYNTHESIS OF A COMPOUND IDENTICAL WITH THE L-CASEI FACTOR ISOLATED FROM LIVER [J].
ANGIER, RB ;
BOOTHE, JH ;
HUTCHINGS, BL ;
MOWAT, JH ;
SEMB, J ;
STOKSTAD, ELR ;
SUBBAROW, Y ;
WALLER, CW ;
COSULICH, DB ;
FAHRENBACH, MJ ;
HULTQUIST, ME ;
KUH, E ;
NORTHEY, EH ;
SEEGER, DR ;
SICKELS, JP ;
SMITH, JM .
SCIENCE, 1945, 102 (2644) :227-228
[7]   Increased methotrexate polyglutamylation in acute megakaryocytic leukemia (M7) compared to other subtypes of acute myelocytic leukemia [J].
Argiris, A ;
Longo, GSA ;
Gorlick, R ;
Tong, W ;
Steinherz, P ;
Bertino, JR .
LEUKEMIA, 1997, 11 (06) :886-889
[8]  
ARKIN H, 1989, CANCER RES, V49, P6556
[9]   Loss of folic acid exporter function with markedly augmented folate accumulation in lipophilic antifolate-resistant mammalian cells [J].
Assaraf, YG ;
Goldman, ID .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (28) :17460-17466
[10]  
AYUSAWA D, 1981, CANCER RES, V41, P1497