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USP6的生理作用及治疗意义。

Physiological roles and therapeutic implications of USP6.

作者信息

Syed Suaad, Painda Muhammad Yasir Khan, Ghafoor Dawood, Gu Dongjin, Wang Feng

机构信息

Key Laboratory of Molecular Medicine and Biotherapy, School of Life Science, Beijing Institute of Technology, Beijing, 100081, China.

School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing, 100081, China.

出版信息

Cell Death Discov. 2025 May 10;11(1):231. doi: 10.1038/s41420-025-02466-0.

Abstract

Ubiquitin-specific protease 6 (USP6) is a member of deubiquitinating enzyme family, recognized for its essential roles in physiological and pathological processes. USP6 is initially identified as a hominoid-specific enzyme residing on chromosome 17p13. USP6 is involved in regulating cellular functions, signaling pathways, protein degradation, intracellular trafficking, tumorigenesis and immune responses. USP6 is pivotal in signaling pathways, including NF-κB, JAK-STAT, and Wnt, which are fundamental for maintaining cellular homeostasis and mediating stress responses. Dysregulation of USP6 has been implicated in a spectrum of diseases, including bone tumors, breast and colorectal cancers, cranial fasciitis, and neurological disorders such as memory dysfunction. Furthermore, USP6 is involved in emerging therapeutic strategies highlighting its implications for drug development. A number of potential small molecule inhibitors are known to be responsible for suppression of USP6, such as Momelotinib (CYT387), FT385, USP30 Inh-1, -2 and -3, 2,6-Diaminopyridine-3,5-bis(thiocyanate) (PR-619) and so on. This review explores the emerging role of USP6 as a key regulator of cellular signaling pathways, its involvement in disease progression, its physiological functions, and the inhibitors that effectively suppress USP6 activity in detail. The comprehensive study provides insight to enhance our understanding of biological importance and therapeutic interventions of USP6 in drug development.

摘要

泛素特异性蛋白酶6(USP6)是去泛素化酶家族的成员,因其在生理和病理过程中的重要作用而闻名。USP6最初被鉴定为定位于17号染色体p13的类人猿特异性酶。USP6参与调节细胞功能、信号通路、蛋白质降解、细胞内运输、肿瘤发生和免疫反应。USP6在信号通路中起关键作用,包括NF-κB、JAK-STAT和Wnt信号通路,这些通路对于维持细胞稳态和介导应激反应至关重要。USP6的失调与一系列疾病有关,包括骨肿瘤、乳腺癌和结直肠癌、颅筋膜炎以及记忆功能障碍等神经疾病。此外,USP6还参与了新兴的治疗策略,凸显了其在药物开发中的意义。已知许多潜在的小分子抑制剂可抑制USP6,如莫洛替尼(CYT387)、FT385、USP30 Inh-1、-2和-3、2,6-二氨基吡啶-3,5-双(硫氰酸盐)(PR-619)等。本综述详细探讨了USP6作为细胞信号通路关键调节因子的新作用、其在疾病进展中的参与情况、其生理功能以及有效抑制USP6活性的抑制剂。这项综合研究为增强我们对USP6在药物开发中的生物学重要性和治疗干预的理解提供了见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e048/12065817/bde00bf2253b/41420_2025_2466_Fig1_HTML.jpg

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