Methotrexate inhibits the glyoxalase system in vivo in children with acute lymphoid leukaemia

被引:26
作者
Bartyik, K
Turi, S
Orosz, F
Karg, E
机构
[1] Univ Szeged, Dept Paediat, Albert Szent Gyorgyi Med Sch, H-6720 Szeged, Hungary
[2] Hungarian Acad Sci, Inst Enzymol, Biol Res Ctr, H-1518 Budapest, Hungary
基金
匈牙利科学研究基金会;
关键词
diabetes; folic acid; folinic acid; glyoxalase; leukaemia; methotrexate; methylglyoxal; D-lactate; thiamine;
D O I
10.1016/j.ejca.2004.06.024
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The inhibition of glyoxalase I leads to antitumour activity through the accumulation of methylglyoxal. Our earlier observations suggested that methotrexate (MTX) may affect the glyoxalase system. This prompted a serial study of the drug on this metabolic pathway. Ten children with acute lymphoid leukaemia (ALL), admitted to our department between January 2002 and July 2003, were enrolled. Plasma D-lactate was assayed before, 24 and 72 h after the start of four consecutive MTX infusions (5 g/m(2)/24 h) in each patient. Inhibition of glyoxalase I was tested in vitro, using human erythrocyte lysates and yeast enzyme. The elevated initial plasma D-lactate levels (P < 0.02) fell significantly (P < 0.001) in response to 24 h MTX infusions. In vitro, MTX, folic and folinic acids inhibited the activity of glyoxalase I. Thus, MTX seems to affect the alpha-oxoaldehyde metabolism in vivo, as a likely consequence of glyoxalase I inhibition. This action probably contributes to the anticancer activity and toxicity of the drug. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2287 / 2292
页数:6
相关论文
共 30 条
[1]   Risk factors for methotrexate-induced lung injury in patients with rheumatoid arthritis - A multicenter, case-control study [J].
Alarcon, GS ;
Kremer, JM ;
Macaluso, M ;
Weinblatt, ME ;
Cannon, GW ;
Palmer, WR ;
StClair, EW ;
Sundy, JS ;
Alexander, RW ;
Smith, GJW ;
Axiotis, CA .
ANNALS OF INTERNAL MEDICINE, 1997, 127 (05) :356-+
[2]   Scavenging system efficiency is crucial for cell resistance to ROS-mediated methylglyoxal injury [J].
Amicarelli, F ;
Colafarina, S ;
Cattani, F ;
Cimini, A ;
Di Ilio, C ;
Ceru, MP ;
Miranda, M .
FREE RADICAL BIOLOGY AND MEDICINE, 2003, 35 (08) :856-871
[3]   A randomized trial of methotrexate in newly diagnosed patients with type 1 diabetes mellitus [J].
Buckingham, BA ;
Sandborg, CI .
CLINICAL IMMUNOLOGY, 2000, 96 (02) :86-90
[4]   POSTPRANDIAL PLASMA D-LACTATE CONCENTRATIONS AFTER YOGURT INGESTION [J].
DEVRESE, M ;
BARTH, CA .
ZEITSCHRIFT FUR ERNAHRUNGSWISSENSCHAFT, 1991, 30 (02) :131-137
[5]   URINARY D-LACTATE EXCRETION IN INFANTS WITH NECROTIZING ENTEROCOLITIS [J].
GARCIA, J ;
SMITH, FR ;
CUCINELL, SA .
JOURNAL OF PEDIATRICS, 1984, 104 (02) :268-270
[6]   Diminished blood levels of reduced glutathione and α-tocopherol in two triosephosphate isomerase-deficient brothers [J].
Karg, E ;
Németh, I ;
Horányi, M ;
Pintér, S ;
Vécsei, L ;
Hollán, S .
BLOOD CELLS MOLECULES AND DISEASES, 2000, 26 (01) :91-100
[7]  
KRAUS JL, 1988, RES COMMUN CHEM PATH, V59, P419
[8]   INHIBITION OF THYMIDYLATE SYNTHASE BY THE DIASTEREOISOMERS OF LEUCOVORIN [J].
LEE, PP ;
SCHILSKY, RL .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1990, 26 (04) :273-277
[9]   Methotrexate hepatotoxicity in psoriatics: Report of 104 patients from Nova Scotia, with analysis of risks from obesity, diabetes and alcohol consumption during long term follow-up [J].
Malatjalian, DA ;
Williams, CN ;
Colwell, SJ ;
Eastwood, BJ .
CANADIAN JOURNAL OF GASTROENTEROLOGY, 1996, 10 (06) :369-375
[10]   FLUOROMETRIC ASSAY OF D-LACTATE [J].
MCLELLAN, AC ;
PHILLIPS, SA ;
THORNALLEY, PJ .
ANALYTICAL BIOCHEMISTRY, 1992, 206 (01) :12-16