Watson Gregory, Ronai Ze'ev A, Lau Eric
Department of Tumor Biology and Program in Chemical Biology and Molecular Medicine, H. Lee Moffitt Cancer Center, Tampa, FL, USA.
Tumor Initiation and Maintenance Program, Cancer Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, USA; Technion Integrated Cancer Center, Rappaport Faculty of Medicine, Technion, Haifa, 3109601, Israel.
Pharmacol Res. 2017 May;119:347-357. doi: 10.1016/j.phrs.2017.02.004. Epub 2017 Feb 15.
Stringent transcriptional regulation is crucial for normal cellular biology and organismal development. Perturbations in the proper regulation of transcription factors can result in numerous pathologies, including cancer. Thus, understanding how transcription factors are regulated and how they are dysregulated in disease states is key to the therapeutic targeting of these factors and/or the pathways that they regulate. Activating transcription factor 2 (ATF2) has been studied in a number of developmental and pathological conditions. Recent findings have shed light on the transcriptional, post-transcriptional, and post-translational regulatory mechanisms that influence ATF2 function, and thus, the transcriptional programs coordinated by ATF2. Given our current knowledge of its multiple levels of regulation and function, ATF2 represents a paradigm for the mechanistic complexity that can regulate transcription factor function. Thus, increasing our understanding of the regulation and function of ATF2 will provide insights into fundamental regulatory mechanisms that influence how cells integrate extracellular and intracellular signals into a genomic response through transcription factors. Characterization of ATF2 dysfunction in the context of pathological conditions, particularly in cancer biology and response to therapy, will be important in understanding how pathways controlled by ATF2 or other transcription factors might be therapeutically exploited. In this review, we provide an overview of the currently known upstream regulators and downstream targets of ATF2.
严格的转录调控对于正常的细胞生物学和机体发育至关重要。转录因子调控失常会导致包括癌症在内的多种病理状况。因此,了解转录因子如何被调控以及它们在疾病状态下如何失调,是针对这些因子和/或它们所调控的信号通路进行治疗的关键。在许多发育和病理状况中都对激活转录因子2(ATF2)进行了研究。最近的研究结果揭示了影响ATF2功能的转录、转录后和翻译后调控机制,进而揭示了由ATF2协调的转录程序。鉴于我们目前对其多层次调控和功能的了解,ATF2代表了调控转录因子功能的机制复杂性的一个范例。因此,加深我们对ATF2调控和功能的理解将有助于深入了解基本的调控机制,这些机制影响细胞如何通过转录因子将细胞外和细胞内信号整合为基因组反应。在病理状况下,特别是在癌症生物学和对治疗的反应中,对ATF2功能障碍的特征进行描述,对于理解由ATF2或其他转录因子控制的信号通路如何用于治疗具有重要意义。在这篇综述中,我们概述了目前已知的ATF2的上游调节因子和下游靶点。