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Enzymes of the one-carbon folate metabolism as anticancer targets predicted by survival rate analysis

机译:单碳叶酸代谢作为抗癌目标通过存活率分析预测的酶

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The significance of mitochondrial metabolism in cancer cells has recently been gaining attention. Among other findings, One-carbon folate metabolism has been reported to be closely associated with cellular characteristics in cancer. To study molecular targets for efficient cancer therapy, we investigated the association between the expressions of genes that code enzymes involved in one-carbon metabolism and survival rate of patients with adenocarcinomas of the colorectum and lung. Patients with high expression of genes that control the metabolic cycle of tetrahydrofolate (THF) in mitochondria, SHMT2, MTHFD2, and ALDH1L2, have a shorter overall survival rate compared with patients with low expression of these genes. Our results revealed that these genes could be novel and more promising anticancer targets than dihydrofolate reductase (DHFR), the current target of drug therapy linked with folate metabolism, suggesting the rationale of drug discovery in cancer medicine.
机译:最近对癌细胞中线粒体代谢的重要性最近一直在受到关注。在其他发现中,据报道,据报道单碳叶酸代谢与癌症中的细胞特征密切相关。为了研究高效癌症治疗的分子靶标,我们研究了涉及结肠癌和肺腺癌患者的一碳代谢和存活率的代谢酶的基因表达之间的关联。在线粒体,SHMT2,MTHFD2和ALDH1L2中控制四氢溶胶(THF)代谢循环的高表达的患者,与这些基因的低表达患者相比,对整体存活率较短。我们的研究结果表明,这些基因可以是新的和更有前途的抗癌目标,而不是二氢酚还原酶(DHFR),目前与叶酸代谢相关的药物治疗的目前的靶标,表明癌症药物发现的药物发现的理由。

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