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The DYRK Family of Kinases in Cancer: Molecular Functions and Therapeutic Opportunities

机译:癌症中激酶的Dyrk系列:分子功能和治疗机会

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摘要

DYRK (dual-specificity tyrosine-regulated kinases) are an evolutionary conserved family of protein kinases with members from yeast to humans. In humans, DYRKs are pleiotropic factors that phosphorylate a broad set of proteins involved in many different cellular processes. These include factors that have been associated with all the hallmarks of cancer, from genomic instability to increased proliferation and resistance, programmed cell death, or signaling pathways whose dysfunction is relevant to tumor onset and progression. In accordance with an involvement of DYRK kinases in the regulation of tumorigenic processes, an increasing number of research studies have been published in recent years showing either alterations of DYRK gene expression in tumor samples and/or providing evidence of DYRK-dependent mechanisms that contribute to tumor initiation and/or progression. In the present article, we will review the current understanding of the role of DYRK family members in cancer initiation and progression, providing an overview of the small molecules that act as DYRK inhibitors and discussing the clinical implications and therapeutic opportunities currently available.
机译:司司(双特异性酪氨酸调节激酶​​)是一种进化保守的蛋白激酶系,其成员来自酵母对人类。在人类中,Dyrkes是磷酸化因素,磷酸化涉及许多不同细胞过程的广泛蛋白质。这些包括与癌症的所有标志相关的因素,从基因组不稳定性增加增加的增殖和抗性,细胞死亡,或信号传导途径,其功能障碍与肿瘤发作和进展相关。根据Dyrk激酶在调节致瘤过程中,近年来发表了越来越多的研究研究,显示肿瘤样本中的羟基基因表达的改变和/或提供有助于的职权机制的证据肿瘤启动和/或进展。在本文中,我们将审查目前对Dyrk家族成员在癌症启动和进展中作用的理解,概述了充当Dyrk抑制剂的小分子,并讨论目前可用的临床意义和治疗机会。

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