Relationship between the efficacy and adverse effects of methotrexate and gene polymorphism

IF 1.1 Q4 GENETICS & HEREDITY Egyptian Journal of Medical Human Genetics Pub Date : 2024-08-04 DOI:10.1186/s43042-024-00562-x
Xin Zhao, Pan Wu, Zhi Yang, Rong-Rong Miao
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Abstract

Methotrexate is a widely used drug in clinical practice for the treatment of collagen vascular diseases and malignant tumors. It has good anti-inflammatory and anti-proliferative effects, but the cytotoxicity of methotrexate can cause various adverse reactions in patients. Studies have shown that the sensitivity and tolerance of different individuals to methotrexate is different. There are many reasons for this difference. Among them, genetic polymorphism is one of the main factors that cause individual differences. This article provides an overview of the genetic polymorphisms of key proteins involved in methotrexate metabolism and transport, such as MTHFR, FPGS, γ-GGH, ABC transporter, OATPs, SLC, TS and DHFR, are related to their efficacy and adverse reactions. The aim is to clarify the impact of genetic polymorphisms on the efficacy and adverse effects of methotrexate at the pharmacogenomic level, in order to provide a basis for the clinical application of methotrexate.
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甲氨蝶呤的疗效和不良反应与基因多态性的关系
甲氨蝶呤是临床上广泛用于治疗胶原血管疾病和恶性肿瘤的药物。它具有良好的抗炎和抗增殖作用,但甲氨蝶呤的细胞毒性会给患者带来各种不良反应。研究表明,不同个体对甲氨蝶呤的敏感性和耐受性是不同的。造成这种差异的原因有很多。其中,基因多态性是造成个体差异的主要因素之一。本文概述了参与甲氨蝶呤代谢和转运的关键蛋白(如 MTHFR、FPGS、γ-GGH、ABC 转运体、OATPs、SLC、TS 和 DHFR)的基因多态性与其疗效和不良反应的关系。目的是在药物基因组学层面阐明基因多态性对甲氨蝶呤疗效和不良反应的影响,为甲氨蝶呤的临床应用提供依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Egyptian Journal of Medical Human Genetics
Egyptian Journal of Medical Human Genetics Medicine-Genetics (clinical)
CiteScore
2.20
自引率
7.70%
发文量
150
审稿时长
18 weeks
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