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通过计算方法和生物学验证发现具有抗肺癌活性的人乳酸脱氢酶 5 抑制剂(hLDH5)。

Discovery of human lactate dehydrogenase 5 inhibitors (hLDH5) with anti-lung cancer activity through an in silico method and biological validation.

机构信息

Department of Oncology, The 5th Affiliated Hospital of Shenzhen University Health Science Center, Shenzhen 518102, China; Key Laboratory of Diagnosis and Treatment of Digestive System Tumors of Zhejiang Province, Hwa Mei Hospital, University of Chinese Academy of Sciences, Ningbo 315010, China.

Department of Oncology, The 5th Affiliated Hospital of Shenzhen University Health Science Center, Shenzhen 518102, China.

出版信息

Bioorg Med Chem Lett. 2019 Sep 1;29(17):2459-2463. doi: 10.1016/j.bmcl.2019.07.029. Epub 2019 Jul 19.

Abstract

Human lactate dehydrogenase 5 (hLDH5) is an important metabolic enzyme playing critical roles in the anaerobic glycolysis. Herein, we employed an in silico method and biological validation to identify a novel hLDH5 inhibitor with a promising cellular activity under hypoxia condition. The identified compound 9 bound to hLDH5 with a K value of 1.02 µM, and inhibited the enzyme with an EC value of 0.7 µM. Compound 9 exhibited a weak potency against NCI-H1975 cell proliferation under normal condition (IC = 36.5 µM), while dramatically increased to 5.7 µM under hypoxia condition. In line with the observation, hLDH5 expression in NCI-H1975 cell under hypoxia condition is much higher as compared to the normal oxygenated condition, indicating the hLDH5 inhibition may contribute to the cancer cell death.

摘要

人源乳酸脱氢酶 5(hLDH5)是一种重要的代谢酶,在无氧糖酵解中发挥关键作用。在此,我们采用了一种计算机模拟方法和生物学验证,以鉴定一种新型 hLDH5 抑制剂,该抑制剂在低氧条件下具有有前途的细胞活性。鉴定出的化合物 9 与 hLDH5 的结合 K 值为 1.02 µM,对酶的抑制 EC 值为 0.7 µM。化合物 9 在正常条件下对 NCI-H1975 细胞增殖的抑制活性较弱(IC = 36.5 µM),但在低氧条件下显著增加至 5.7 µM。与观察结果一致的是,与正常氧合条件相比,hLDH5 在 NCI-H1975 细胞中的表达在低氧条件下要高得多,这表明 hLDH5 抑制可能有助于癌细胞死亡。

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