Mechanisms underlying methotrexate-induced pulmonary toxicity

Authors
Kim, Youn-JungSong, MeeRyu, Jae-Chun
Issue Date
2009-07
Publisher
TAYLOR & FRANCIS LTD
Citation
EXPERT OPINION ON DRUG SAFETY, v.8, no.4, pp.451 - 458
Abstract
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.
Keywords
ACTIVATED PROTEIN-KINASE; LOW-DOSE METHOTREXATE; INTERSTITIAL LUNG-DISEASES; BLOOD MONONUCLEAR-CELLS; RHEUMATOID-ARTHRITIS; GENE-EXPRESSION; ALVEOLAR MACROPHAGES; INDUCED PNEUMONITIS; EPITHELIAL-CELLS; HYPERSENSITIVITY PNEUMONITIS; ACTIVATED PROTEIN-KINASE; LOW-DOSE METHOTREXATE; INTERSTITIAL LUNG-DISEASES; BLOOD MONONUCLEAR-CELLS; RHEUMATOID-ARTHRITIS; GENE-EXPRESSION; ALVEOLAR MACROPHAGES; INDUCED PNEUMONITIS; EPITHELIAL-CELLS; HYPERSENSITIVITY PNEUMONITIS; mechanism; methotrexate; p38 MAPK; pulmonary toxicity
ISSN
1474-0338
URI
https://pubs.kist.re.kr/handle/201004/132373
DOI
10.1517/14740330903066734
Appears in Collections:
KIST Article > 2009
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