Cuthbertson Christine R, Guo Hui, Kyani Armita, Madak Joseph T, Arabzada Zahra, Neamati Nouri
Department of Medicinal Chemistry, College of Pharmacy and the Rogel Cancer Center, University of Michigan, North Campus Research Complex, 1600 Huron Parkway, Ann Arbor, Michigan 48109, United States.
ACS Pharmacol Transl Sci. 2020 Nov 23;3(6):1242-1252. doi: 10.1021/acsptsci.0c00124. eCollection 2020 Dec 11.
The dihydroorotate dehydrogenase (DHODH) inhibitor brequinar failed all clinical trials for solid tumors. To investigate mechanisms to increase brequinar's efficacy, we employed a combination strategy to simultaneously inhibit the nucleotide salvage pathways. Brequinar is synergistic with the equilibrative nucleoside transporter (ENT) inhibitor dipyridamole, but not the concentrative nucleoside transporter inhibitor phlorizin. This synergy carries over to ENT1/2 inhibition, but not ENT4. Our previously described brequinar analogue was also synergistic with dipyridamole as were the FDA-approved DHODH inhibitors leflunomide and teriflunomide but the latter required much higher concentrations than brequinar. Therefore, a combination of brequinar and ENT inhibitors presents a potential anti-cancer strategy in select tumors.
二氢乳清酸脱氢酶(DHODH)抑制剂布喹那在实体瘤的所有临床试验中均告失败。为了探究提高布喹那疗效的机制,我们采用了联合策略来同时抑制核苷酸补救途径。布喹那与平衡核苷转运体(ENT)抑制剂双嘧达莫具有协同作用,但与钠依赖性核苷转运体抑制剂根皮苷没有协同作用。这种协同作用在ENT1/2抑制中存在,但在ENT4抑制中不存在。我们之前描述的布喹那类似物与双嘧达莫也具有协同作用,美国食品药品监督管理局(FDA)批准的DHODH抑制剂来氟米特和特立氟胺也是如此,但后者所需浓度比布喹那高得多。因此,布喹那与ENT抑制剂联合使用在某些肿瘤中呈现出一种潜在的抗癌策略。