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ACK1/TNK2激酶:分子机制与新兴的癌症治疗方法

ACK1/TNK2 kinase: molecular mechanisms and emerging cancer therapeutics.

作者信息

Sridaran Dhivya, Mahajan Nupam P

机构信息

Division of Urologic Surgery, Department of Surgery, Washington University at St. Louis, St. Louis, MO 63110, USA.

Division of Urologic Surgery, Department of Surgery, Washington University at St. Louis, St. Louis, MO 63110, USA; Siteman Cancer Center, Cancer Research Building, Washington University at St. Louis, St. Louis, MO 63110, USA.

出版信息

Trends Pharmacol Sci. 2025 Jan;46(1):62-77. doi: 10.1016/j.tips.2024.11.006. Epub 2024 Dec 24.

Abstract

Activated CDC42-associated kinase 1 (ACK1), encoded by the TNK2 gene, is a cytoplasmic non-receptor tyrosine kinase whose aberrant activation correlates positively with cancer severity. Recent research has revealed the functional relevance of this oncokinase - it is an epigenetic regulator that drives cancer progression in multiple malignancies. Although ACK1 is an attractive target for therapeutic intervention, incomplete knowledge of its diverse signaling mechanisms and the lack of specific inhibitors have challenged its clinical success. We summarize recent breakthroughs in understanding ACK1 regulation and cellular signaling, and shed light on its immunomodulatory role in balancing T cell activation. We provide a comprehensive overview of preclinical, proof-of-concept studies of potent ACK1-targeting small-molecule inhibitors that are expected to enter clinical trials for cancer patients.

摘要

由TNK2基因编码的活化的CDC42相关激酶1(ACK1)是一种细胞质非受体酪氨酸激酶,其异常激活与癌症严重程度呈正相关。最近的研究揭示了这种致癌激酶的功能相关性——它是一种表观遗传调节剂,可在多种恶性肿瘤中推动癌症进展。尽管ACK1是治疗干预的一个有吸引力的靶点,但其多样的信号传导机制了解不全面以及缺乏特异性抑制剂对其临床应用成功构成了挑战。我们总结了在理解ACK1调节和细胞信号传导方面的最新突破,并阐明了其在平衡T细胞激活中的免疫调节作用。我们全面概述了针对ACK1的强效小分子抑制剂的临床前概念验证研究,这些抑制剂有望进入癌症患者的临床试验。

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