Instituto de Parasitología y Biomedicina López Neyra, CSIC, CIBERONC, 18016, Granada, Spain.
Centro de Investigación Biomédica en Red de Cáncer, CIBERONC, 28029, Madrid, Spain.
J Exp Clin Cancer Res. 2021 Apr 28;40(1):144. doi: 10.1186/s13046-021-01950-6.
Tankyrase 1 (TNKS1) and tankyrase 2 (TNKS2) are two homologous proteins that are gaining increasing importance due to their implication in multiple pathways and diseases such as cancer. TNKS1/2 interact with a large variety of substrates through the ankyrin (ANK) domain, which recognizes a sequence present in all the substrates of tankyrase, called Tankyrase Binding Motif (TBM). One of the main functions of tankyrases is the regulation of protein stability through the process of PARylation-dependent ubiquitination (PARdU). Nonetheless, there are other functions less studied that are also essential in order to understand the role of tankyrases in many pathways. In this review, we concentrate in different tankyrase substrates and we analyze in depth the biological consequences derived of their interaction with TNKS1/2. We also examine the concept of both canonical and non-canonical TBMs and finally, we focus on the information about the role of TNKS1/2 in different tumor context, along with the benefits and limitations of the current TNKS inhibitors targeting the catalytic PARP domain and the novel strategies to develop inhibitors against the ankyrin domain. Available data indicates the need for further deepening in the knowledge of tankyrases to elucidate and improve the current view of the role of these PARP family members and get inhibitors with a better therapeutic and safety profile.
Tankyrase 1 (TNKS1) 和 tankyrase 2 (TNKS2) 是两种同源蛋白,由于它们在多种途径和疾病(如癌症)中的作用,越来越受到重视。TNKS1/2 通过锚蛋白(ANK)结构域与多种底物相互作用,该结构域识别 tankyrase 所有底物中存在的序列,称为 Tankyrase Binding Motif (TBM)。tankyrases 的主要功能之一是通过 PARylation 依赖性泛素化(PARdU)过程调节蛋白质稳定性。然而,还有其他研究较少的功能对于理解 tankyrases 在许多途径中的作用也很重要。在这篇综述中,我们集中讨论了不同的 tankyrase 底物,并深入分析了它们与 TNKS1/2 相互作用所产生的生物学后果。我们还研究了规范和非规范 TBM 的概念,最后,我们关注 TNKS1/2 在不同肿瘤环境中的作用的信息,以及针对催化 PARP 结构域的 TNKS 抑制剂的现有益处和局限性,以及针对锚蛋白结构域开发抑制剂的新策略。现有数据表明,需要进一步深入了解 tankyrases,以阐明和改善这些 PARP 家族成员作用的现有观点,并获得具有更好治疗和安全性的抑制剂。