Identification of human LDHC4 as a potential target for anticancer drug discovery

被引:4
|
作者
Tan, Hong [1 ]
Wang, Huali [2 ,3 ]
Ma, Jinhu [2 ,3 ]
Deng, Hui [4 ]
He, Qinghua [5 ]
Chen, Qiang [2 ,3 ]
Zhang, Qinglian [4 ]
机构
[1] Southwest Minzu Univ, Res Inst Qinghai Tibet Plateau, Chengdu 610041, Peoples R China
[2] Sichuan Univ, West China Hosp, State Key Lab Biotherapy & Canc Ctr, Chengdu 610041, Peoples R China
[3] Collaborat Innovat Ctr Biotherapy, Chengdu 610041, Peoples R China
[4] Chengdu Med Coll, Sch Lab Med, Chengdu 610500, Peoples R China
[5] Southwest Minzu Univ, Key Lab Qinghai Tibetan Plateau Anim Genet Resour, Chengdu 610041, Peoples R China
基金
中国国家自然科学基金;
关键词
LDHC; Anticancer target; Warburg effect; LDHC4; structure; (Ethylamino) (oxo)acetic acid; LDH isoforms; Lung cancer; Tissue microarray; LACTATE-DEHYDROGENASE-C; EXPRESSION; INHIBITION; CELLS; ATTENUATION; REDUCTION; ISOZYME; GROWTH; MODEL; APO;
D O I
10.1016/j.apsb.2021.12.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
One of the distinct hallmarks of cancer cells is aerobic glycolysis (Warburg effect). Lactate dehydrogenase A (LDHA) is thought to play a key role in aerobic glycolysis and has been extensively studied, while lactate dehydrogenase C (LDHC), an isoform of LDHA, has received much less attention. Here we showed that human LDHC was significantly expressed in lung cancer tissues, overexpression of Ldhc in mice could promote tumor growth, and knock-down of LDHC could inhibit the proliferation of lung cancer A549 cells. We solved the first crystal structure of human LDHC4 and found that the active-site loop of LDHC4 adopted a distinct conformation compared to LDHA4 and lactate dehydrogenase B4 (LDHB4). Moreover, we found that (ethylamino) (oxo)acetic acid shows about 10 times selective inhi-bition against LDHC4 over LDHA4 and LDHB4. Our studies suggest that LDHC4 is a potential target for anticancer drug discovery and (ethylamino) (oxo)acetic acid provides a good start to develop lead compounds for selective drugs targeting LDHC4.(C) 2022 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V.
引用
收藏
页码:2348 / 2357
页数:10
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