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靶向亚甲基四氢叶酸脱氢酶2的抗癌药物发现

Drug discovery of anticancer drugs targeting methylenetetrahydrofolate dehydrogenase 2.

作者信息

Asai Ayumu, Koseki Jun, Konno Masamitsu, Nishimura Tatsunori, Gotoh Noriko, Satoh Taroh, Doki Yuichiro, Mori Masaki, Ishii Hideshi

机构信息

Department of Medical Data Science, Graduate School of Medicine, Osaka University, Suita 565-0871, Japan.

Department of Frontier Science for Cancer and Chemotherapy, Graduate School of Medicine, Osaka University, Suita 565-0871, Japan.

出版信息

Heliyon. 2018 Dec 17;4(12):e01021. doi: 10.1016/j.heliyon.2018.e01021. eCollection 2018 Dec.

Abstract

Many anticancer drugs have serious adverse effects; therefore, it is necessary to target features specific to cancer cells to minimize the effects on healthy cells. Methylenetetrahydrofolate dehydrogenase 2 (MTHFD2) was reported to be specifically enhanced in cancer. We confirmed the validity of MTHFD2 as a drug discovery target using clinical data. In addition, we performed screening to design an anticancer drug specifically targeting MTHFD2. Analysis of the clinical data indicated that MTHFD2 was enhanced in most cancers compared with normal tissues, and affected the prognosis in cancer patients. Candidate compounds for MTHFD2 inhibitors were identified using drug discovery techniques, and the important interactions for MTHFD2 binding were determined. In addition, these candidate compounds decreased levels of MTHFD2 metabolites in cancer cells. The findings of the present study may help to develop anticancer drugs targeting MTHFD2, with a view to minimizing the adverse effects of anticancer drugs.

摘要

许多抗癌药物都有严重的副作用;因此,有必要针对癌细胞特有的特征,以尽量减少对健康细胞的影响。据报道,亚甲基四氢叶酸脱氢酶2(MTHFD2)在癌症中特异性增强。我们利用临床数据证实了MTHFD2作为药物发现靶点的有效性。此外,我们进行了筛选以设计一种特异性靶向MTHFD2的抗癌药物。临床数据分析表明,与正常组织相比,MTHFD2在大多数癌症中均有增强,并影响癌症患者的预后。利用药物发现技术鉴定了MTHFD2抑制剂的候选化合物,并确定了MTHFD2结合的重要相互作用。此外,这些候选化合物降低了癌细胞中MTHFD2代谢物的水平。本研究结果可能有助于开发靶向MTHFD2的抗癌药物,以尽量减少抗癌药物的副作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03bd/6299143/fb45543b42c4/gr1.jpg

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