Sabanés Zariquiey Francesc, da Souza João V, Estrada-Tejedor Roger, Bronowska Agnieszka K
Chemistry, School of Natural and Environmental Sciences, Newcastle University, NE1 7RU Newcastle, United Kingdom.
IQS School of Engineering(IQS)-Universitat Ramon Llull (URL), 08017 Barcelona, Spain.
ACS Omega. 2019 Aug 15;4(9):13913-13921. doi: 10.1021/acsomega.9b01601. eCollection 2019 Aug 27.
Signal transducer activator of transcription 3 (STAT3) is among the most investigated oncogenic transcription factors, as it is highly associated with cancer initiation, progression, metastasis, chemoresistance, and immune evasion. Evidences from both preclinical and clinical studies have demonstrated that STAT3 plays a critical role in several malignancies associated with poor prognosis such as glioblastoma and triple-negative breast cancer, and STAT3 inhibitors have shown efficacy in inhibiting cancer growth and metastasis. Constitutive activation of STAT3 by mutations occurs frequently in tumor cells and directly contributes to many malignant phenotypes. Unfortunately, detailed structural biology studies on STAT3 as well as target-based drug discovery efforts have been hampered by difficulties in the expression and purification of the full-length STAT3 and a lack of ligand-bound crystal structures. Considering these, molecular modeling and simulations offer an attractive strategy for the assessment of the "druggability" of STAT3 dimers and allow investigations of reported activating and inhibiting STAT3 mutants at the atomistic level of detail. In the present study, we focused on the effects exerted by reported STAT3 mutations on the protein structure, dynamics, DNA-binding, and dimerization, thus linking structure, dynamics, energetics, and the biological function. By employing atomistic molecular dynamics and umbrella-sampling simulations to a series of human STAT3 dimers, which comprised wild-type protein and four mutations, we explained the modulation of STAT3 activity by these mutations. Counter-intuitively, our results show that the D570K inhibitory mutation exerts its effect by enhancing rather than weakening STAT3-DNA interactions, which interfere with the DNA release by the protein dimer and thus inhibit STAT3 function as a transcription factor. We mapped the binding site and characterized the binding mode of a clinical candidate napabucasin/BBI-608 at STAT3, which resembles the effect of a D570K mutation. Our results contribute to understanding the activation/inhibition mechanism of STAT3, to explain the molecular mechanism of STAT3 inhibition by BBI-608. Alongside the characterization of the BBI-608 binding mode, we also discovered a novel binding site amenable to bind small-molecule ligands, which may pave the way to design novel STAT3 inhibitors and to suggest new strategies for pharmacological interventions to combat cancers associated with poor prognosis.
信号转导和转录激活因子3(STAT3)是研究最多的致癌转录因子之一,因为它与癌症的发生、发展、转移、化疗耐药及免疫逃逸高度相关。临床前和临床研究的证据均表明,STAT3在胶质母细胞瘤和三阴性乳腺癌等多种预后不良的恶性肿瘤中起关键作用,且STAT3抑制剂已显示出抑制癌症生长和转移的功效。肿瘤细胞中常因突变导致STAT3组成型激活,这直接促成了许多恶性表型。不幸的是,由于全长STAT3的表达和纯化困难以及缺乏配体结合晶体结构,阻碍了对STAT3的详细结构生物学研究以及基于靶点的药物研发工作。考虑到这些,分子建模和模拟为评估STAT3二聚体的“成药性”提供了一种有吸引力的策略,并允许在原子水平详细研究已报道的激活和抑制STAT3的突变体。在本研究中,我们聚焦于已报道的STAT3突变对蛋白质结构、动力学、DNA结合及二聚化的影响,从而将结构、动力学、能量学与生物学功能联系起来。通过对一系列包含野生型蛋白和四种突变的人类STAT3二聚体进行原子水平的分子动力学和伞形采样模拟,我们解释了这些突变对STAT3活性的调节作用。与直觉相反,我们的结果表明,D570K抑制性突变通过增强而非减弱STAT3与DNA的相互作用发挥作用,这种相互作用干扰了蛋白质二聚体释放DNA,从而抑制STAT3作为转录因子的功能。我们确定了临床候选药物萘布卡生/BBI - 608在STAT3上的结合位点并表征了其结合模式,该模式类似于D570K突变的作用。我们的结果有助于理解STAT3的激活/抑制机制,解释BBI - 608抑制STAT