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去泛素化酶在原发性骨癌中的作用

The Role of Deubiquitinating Enzymes in Primary Bone Cancer.

作者信息

Colaco Jencia Carminha, Suresh Bharathi, Kaushal Kamini, Singh Vijai, Ramakrishna Suresh

机构信息

Graduate School of Biomedical Science and Engineering, Hanyang University, Seoul, 04763, South Korea.

Department of Biosciences, School of Science, Indrashil University, Rajpur, Mehsana, Gujarat, 382715, India.

出版信息

Mol Biotechnol. 2024 Aug 23. doi: 10.1007/s12033-024-01254-y.

Abstract

Bone is a living, intricate, and dynamic tissue providing locomotion and protection of the body. It also performs hematopoiesis and mineral homeostasis. Osteosarcoma (OS), Ewing sarcoma (ES), and chondrosarcoma (CS) are primary bone cancers. OS and ES mostly develop in younger individuals, and CS generally develops in adults. Ubiquitination regulates numerous cellular processes. The deubiquitinating enzymes (DUBs) detach the ubiquitin molecules from the ubiquitin labeled substrate, altering ubiquitinated protein functions and regulating protein stability via various signaling pathways. Protein homeostasis and bone remodeling are both crucially influenced by the UPS. Recently, there have been several reports on DUBs involved in bone homeostasis and various bone disorders through the regulation of osteoblasts and osteoclasts via NF-κB, Wnt/β-catenin, TRAF6, TGFβ, ERK1/2, and PI3K/Akt pathways. However, DUBs regulating function in bone homeostasis is still in its infancy. Here, we summarized several recent identifications on DUBs, with a focus on their role in bone cancer progression. Therefore, the study attempts to summarize association with the expression level of DUBs as key factors driving bone cancers and also provide new insights on DUBs as key pharmacologic targets for bone cancer therapeutics.

摘要

骨骼是一种有生命的、复杂且动态的组织,为身体提供运动功能并起到保护作用。它还参与造血和矿物质稳态调节。骨肉瘤(OS)、尤因肉瘤(ES)和软骨肉瘤(CS)是原发性骨癌。骨肉瘤和尤因肉瘤大多发生于年轻人,而软骨肉瘤一般发生于成年人。泛素化调节众多细胞过程。去泛素化酶(DUBs)将泛素分子从泛素标记的底物上分离下来,通过各种信号通路改变泛素化蛋白的功能并调节蛋白质稳定性。蛋白质稳态和骨重塑均受到泛素蛋白酶体系统(UPS)的关键影响。最近,有几篇报道称,去泛素化酶通过核因子κB(NF-κB)、Wnt/β-连环蛋白、肿瘤坏死因子受体相关因子6(TRAF6)、转化生长因子β(TGFβ)、细胞外信号调节激酶1/2(ERK1/2)和磷脂酰肌醇-3激酶/蛋白激酶B(PI3K/Akt)信号通路对成骨细胞和破骨细胞的调节作用,参与骨稳态维持和各种骨疾病的发生发展。然而,去泛素化酶在骨稳态中的调节功能研究仍处于起步阶段。在此,我们总结了近期关于去泛素化酶的一些研究发现,重点关注它们在骨癌进展中的作用。因此,本研究试图总结去泛素化酶的表达水平与驱动骨癌的关键因素之间的关联,并为将去泛素化酶作为骨癌治疗的关键药理学靶点提供新的见解。

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