Wu Zhuo-Xun, Peng Zheng, Yang Yuqi, Wang Jing-Quan, Teng Qiu-Xu, Lei Zi-Ning, Fu Yi-Ge, Patel Ketankumar, Liu Lili, Lin Lizhu, Zou Chang, Chen Zhe-Sheng
Department of Pharmaceutical Sciences, College of Pharmacy and Health Sciences, St. John's University, Queens, NY, United States.
The Second Clinical Medical College of Jinan University, The First Affiliated Hospital of Southern University of Science and Technology, Shenzhen People's Hospital, Shenzhen, China.
Front Oncol. 2020 May 12;10:674. doi: 10.3389/fonc.2020.00674. eCollection 2020.
M3814, also known as nedisertib, is a potent and selective DNA-dependent protein kinase (DNA-PK) inhibitor under phase 2 clinical trials. ABCG2 is a member of the ATP-binding cassette (ABC) transporter family that is closely related to multidrug resistance (MDR) in cancer treatment. In this study, we demonstrated that M3814 can modulate the function of ABCG2 and overcome ABCG2-mediated MDR. Mechanistic studies showed that M3814 can attenuate the efflux activity of ABCG2 transporter, leading to increased ABCG2 substrate drugs accumulation. Furthermore, M3814 can stimulate the ABCG2 ATPase activity in a concentration-dependent manner without affecting the ABCG2 protein expression or cell surface localization of ABCG2. Moreover, the molecular docking analysis indicated a high affinity between M3814 and ABCG2 transporter at the drug-binding cavity. Taken together, our work reveals M3814 as an ABCG2 modulator and provides a potential combination of co-administering M3814 with ABCG2 substrate-drugs to overcome MDR.
M3814,也被称为奈地西肽,是一种正在进行2期临床试验的强效且选择性的DNA依赖性蛋白激酶(DNA-PK)抑制剂。ABCG2是ATP结合盒(ABC)转运蛋白家族的成员,与癌症治疗中的多药耐药性(MDR)密切相关。在本研究中,我们证明M3814可以调节ABCG2的功能并克服ABCG2介导的多药耐药性。机制研究表明,M3814可以减弱ABCG2转运蛋白的外排活性,导致ABCG2底物药物积累增加。此外,M3814可以以浓度依赖性方式刺激ABCG2的ATP酶活性,而不影响ABCG2蛋白表达或ABCG2的细胞表面定位。此外,分子对接分析表明M3814与ABCG2转运蛋白在药物结合腔处具有高亲和力。综上所述,我们的工作揭示了M3814作为ABCG2调节剂的作用,并提供了将M3814与ABCG2底物药物联合使用以克服多药耐药性的潜在组合。