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MTHFR polymorphisms in childhood acute lymphoblastic leukemia: influence on methotrexate therapy

机译:儿童急性淋巴细胞白血病MTHFR基因多态性:对甲氨蝶呤治疗的影响

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Methotrexate (MTX) is an important component in the therapy used to treat childhood acute lymphoblastic leukemia (ALL). Methylenetetrahydrofolate reductase (MTHFR) is a key enzyme for MTX pharmacokinetics. Two single-nucleotide polymorphisms in MTHFR gene, C677T and A1298C, affecting MTHFR activity, have been widely studied as potential markers of MTX toxicity and/or outcome in pediatric ALL. In this review, we show that the majority of published reports do not find association or present opposite effect. Therefore, MTHFR C677T and A1298C polymorphisms do not seem to be good markers of MTX-related toxicity and/or outcome in pediatric ALL. The efforts should be focused on other genes, such as transporter genes or microRNA-related genes.
机译:甲氨蝶呤(MTX)是用于治疗儿童急性淋巴细胞白血病(ALL)的疗法中的重要组成部分。亚甲基四氢叶酸还原酶(MTHFR)是MTX药代动力学的关键酶。影响MTHFR活性的MTHFR基因中的两个单核苷酸多态性C677T和A1298C已被广泛研究为MTX毒性和/或儿科ALL预后的潜在标志物。在这篇评论中,我们表明大多数已发表的报告都没有发现关联或呈现相反的效果。因此,MTHFR C677T和A1298C多态性似乎不是小儿ALL中MTX相关毒性和/或结果的良好标志。这些工作应集中在其他基因上,例如转运蛋白基因或与microRNA相关的基因。

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