Mechanisms underlying methotrexate-induced pulmonary toxicity

被引:32
作者
Kim, Youn-Jung [1 ]
Song, Mee [1 ]
Ryu, Jae-Chun [1 ]
机构
[1] Korea Inst Sci & Technol, Cellular & Mol Toxicol Lab, Seoul, South Korea
关键词
mechanism; methotrexate; p38; MAPK; pulmonary toxicity; ACTIVATED PROTEIN-KINASE; LOW-DOSE METHOTREXATE; INTERSTITIAL LUNG-DISEASES; BLOOD MONONUCLEAR-CELLS; RHEUMATOID-ARTHRITIS; GENE-EXPRESSION; ALVEOLAR MACROPHAGES; INDUCED PNEUMONITIS; EPITHELIAL-CELLS; HYPERSENSITIVITY PNEUMONITIS;
D O I
10.1517/14740330903066734
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Methotrexate (MTX) has been widely used for the treatment of inflammatory diseases and rheumatoid arthritis, as well as a variety of tumors. However, MTX-induced pulmonary toxicity is a serious and unpredictable side effect of the therapy, which includes allergic, cytotoxic or immunologic reactions, and is a major clinical problem. Objective: To summarize the mechanisms of action involved in MTX-induced pulmonary toxicity. Methods: We reviewed the literature describing MTX-induced adverse pulmonary effects and the mechanisms of action underlying MTX-induced pulmonary toxicity. Conclusion: The mechanisms underlying MTX toxicity are complex. The clinical effects may be attributable to both the anti-inflammatory and immunosuppressive effects of MTX The mechanisms causing the side effects of MTX include mutation of the genotype, inhibition of transport, MTX-polyglutamates and P-glycoprotein binding with MTX The p38 MAPK-signaling pathway is especially associated with a pulmonary inflammatory response. These mechanisms can be applied to optimize drug treatment.
引用
收藏
页码:451 / 458
页数:8
相关论文
共 72 条
[1]   LEUKOCYTE MIGRATION-INHIBITION IN METHOTREXATE-INDUCED PNEUMONITIS - EVIDENCE FOR AN IMMUNOLOGICAL CELL-MEDIATED MECHANISM [J].
AKOUN, GM ;
GAUTHIERRAHMAN, S ;
MAYAUD, CM ;
TOUBOUL, JL ;
DENIS, MF .
CHEST, 1987, 91 (01) :96-99
[2]   Heat shock protein 27 functions in inflammatory gene expression and transforming growth factor-β-activated kinase-1 (TAK1)-mediated signaling [J].
Alford, Kate A. ;
Glennie, Sarah ;
Turrell, Bryony R. ;
Rawlinson, Lesley ;
Saklatvala, Jeremy ;
Dean, Jonathan L. E. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (09) :6232-6241
[3]   LEUKOCYTE ADHERENCE IN RAT MESENTERIC VENULES - EFFECTS OF ADENOSINE AND METHOTREXATE [J].
ASAKO, H ;
WOLF, RE ;
GRANGER, DN .
GASTROENTEROLOGY, 1993, 104 (01) :31-37
[4]   Gene Ontology: tool for the unification of biology [J].
Ashburner, M ;
Ball, CA ;
Blake, JA ;
Botstein, D ;
Butler, H ;
Cherry, JM ;
Davis, AP ;
Dolinski, K ;
Dwight, SS ;
Eppig, JT ;
Harris, MA ;
Hill, DP ;
Issel-Tarver, L ;
Kasarskis, A ;
Lewis, S ;
Matese, JC ;
Richardson, JE ;
Ringwald, M ;
Rubin, GM ;
Sherlock, G .
NATURE GENETICS, 2000, 25 (01) :25-29
[5]  
AURON PE, 1987, J IMMUNOL, V138, P1447
[6]   Novel aspects of resistance to drugs targeted to dihydrofolate reductase and thymidylate synthase [J].
Banerjee, D ;
Mayer-Kuckuk, P ;
Capiaux, G ;
Budak-Alpdogan, T ;
Gorlick, R ;
Bertino, JR .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2002, 1587 (2-3) :164-173
[7]   TRANSFORMING GROWTH FACTOR-BETA-1 IS PRESENT AT SITES OF EXTRACELLULAR-MATRIX GENE-EXPRESSION IN HUMAN PULMONARY FIBROSIS [J].
BROEKELMANN, TJ ;
LIMPER, AH ;
COLBY, TV ;
MCDONALD, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (15) :6642-6646
[8]   Variation of immunological response in methotrexate-induced pneumonitis [J].
Chikura, B. ;
Sathi, N. ;
Lane, S. ;
Dawson, J. K. .
RHEUMATOLOGY, 2008, 47 (11) :1647-1650
[9]   TAK1-mediated stress signaling pathways are essential for TNF-α-promoted pulmonary metastasis of murine colon cancer cells [J].
Choo, MK ;
Sakurai, H ;
Koizumi, K ;
Saiki, I .
INTERNATIONAL JOURNAL OF CANCER, 2006, 118 (11) :2758-2764
[10]   Combination of infliximab and methotrexate therapy for early rheumatoid arthritis - A randomized, controlled trial [J].
Clair, EWS ;
van der Heijde, DMFM ;
Smolen, JS ;
Maini, RN ;
Bathon, JM ;
Emery, P ;
Keystone, E ;
Schiff, M ;
Kalden, JR ;
Wang, B ;
DeWoody, K ;
Weiss, R ;
Baker, D .
ARTHRITIS AND RHEUMATISM, 2004, 50 (11) :3432-3443