Yang Yuqi, Wu Zhuo-Xun, Wang Jing-Quan, Teng Qiu-Xu, Lei Zi-Ning, Lusvarghi Sabrina, Ambudkar Suresh V, Chen Zhe-Sheng, Yang Dong-Hua
Department of Pharmaceutical Sciences, College of Pharmacy and Health Sciences, St. John's University, Queens, NY, United States.
Laboratory of Cell Biology, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD, United States.
Front Pharmacol. 2021 Feb 15;12:620874. doi: 10.3389/fphar.2021.620874. eCollection 2021.
OTS964 is a potent T-LAK cell-originated protein kinase (TOPK) inhibitor. Herein, we investigated the interaction of OTS964 and multidrug resistance (MDR)-associated ATP-binding cassette sub-family G member 2 (ABCG2). The cell viability assay indicated that the effect of OTS964 is limited in cancer drug-resistant and transfected cells overexpressing ABCG2. We found that the known ABCG2 transporter inhibitor has the ability to sensitize ABCG2-overexpressing cells to OTS964. In mechanism-based studies, OTS964 shows inhibitory effect on the efflux function mediated by ABCG2, and in turn, affects the pharmacokinetic profile of other ABCG2 substrate-drugs. Furthermore, OTS964 upregulates ABCG2 protein expression, resulting in enhanced resistance to ABCG2 substrate-drugs. The ATPase assay demonstrated that OTS964 stimulates ATPase activity of ABCG2 in a concentration-dependent manner. The computational molecular docking analysis combined with results from ATPase assay suggested that OTS964 interacts with drug-binding pocket of ABCG2 and has substrate-like behaviors. Thus, OTS964 is an MDR-susceptible agent due to its interactions with ABCG2, and overexpression of ABCG2 transporter may attenuate its therapeutic effect in cancer cells.
OTS964是一种强效的T淋巴细胞来源的蛋白激酶(TOPK)抑制剂。在此,我们研究了OTS964与多药耐药(MDR)相关的ATP结合盒亚家族G成员2(ABCG2)之间的相互作用。细胞活力测定表明,OTS964在癌症耐药细胞和过表达ABCG2的转染细胞中的作用有限。我们发现,已知的ABCG2转运体抑制剂能够使过表达ABCG2的细胞对OTS964敏感。在基于机制的研究中,OTS964对ABCG2介导的外排功能具有抑制作用,进而影响其他ABCG2底物药物的药代动力学特征。此外,OTS964上调ABCG2蛋白表达,导致对ABCG2底物药物的耐药性增强。ATP酶测定表明,OTS964以浓度依赖的方式刺激ABCG2的ATP酶活性。计算分子对接分析结合ATP酶测定结果表明,OTS964与ABCG2的药物结合口袋相互作用,并具有类似底物的行为。因此,由于OTS964与ABCG2的相互作用,它是一种MDR敏感剂,并且ABCG2转运体的过表达可能会减弱其在癌细胞中的治疗效果。