Discovery of human lactate dehydrogenase A (LDHA) inhibitors as anticancer agents to inhibit the proliferation of MG-63 osteosarcoma cells

被引:21
|
作者
Fang, Aiping [1 ]
Zhang, Qi [1 ]
Fan, Haibo
Zhou, Yaying [1 ,2 ,3 ]
Yao, Yuqin
Zhang, Yue [1 ,3 ]
Huang, Xiaojun [2 ]
机构
[1] Sichuan Univ, West China Sch Publ Health, Chengdu 610041, Sichuan, Peoples R China
[2] Sichuan Univ, West China Hosp, State Key Lab Biotherapy Collaborat Innovat Ctr B, Chengdu 610041, Sichuan, Peoples R China
[3] Jinan Univ, Clin Med Coll 2, Shenzhen 518020, Peoples R China
关键词
TUMOR PROGRESSION; CANCER-THERAPY; LUNG-CANCER; GOSSYPOL; IDENTIFICATION; EXPRESSION; GENERATION; CARCINOMA; GROWTH; LINES;
D O I
10.1039/c7md00222j
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Human lactate dehydrogenase A (LDHA) has been identified as a potential therapeutic target in the area of cancer metabolism. Herein, we report the discovery of novel LDHA inhibitors through docking-based virtual screening and biological assays. The primary enzymatic assay suggested that compound 11 targeted LDHA with an IC50 value of 0.33 mu M. The in vitro cytotoxic assay demonstrated that compound 11 reduced the growth of MG-63 cancer cells with an EC50 value of 3.35 mu M. Finally, we found that compound 11 induced the apoptosis of MG-63 cancer cells in a dose dependent manner, upregulated the oxygen consumption rate (OCR), and decreased the lactate formation and extracellular acidification rate (ECAR) in MG-63 cancer cells. Collectively, our data suggested that compound 11 could be a promising lead for the development of potent LDHA inhibitors.
引用
收藏
页码:1720 / 1726
页数:7
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