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去泛素化酶在癌症代谢中作为治疗靶点的新作用。

The emerging role of deubiquitylating enzymes as therapeutic targets in cancer metabolism.

作者信息

Tu Rongfu, Ma Junpeng, Zhang Peng, Kang Ye, Xiong Xiaofan, Zhu Junsheng, Li Miao, Zhang Chengsheng

机构信息

Precision Medicine Center, The First Affiliated Hospital of Xi'an Jiaotong University, 277 Yanta West Road, Xi'an, 710061, China.

Department of Cancer Precision Medicine, The MED-X Institute, The First Affiliated Hospital of Xi'an Jiaotong University, Building 21, Western China Science and Technology Innovation Harbor, Xi'an, 710000, China.

出版信息

Cancer Cell Int. 2022 Mar 20;22(1):130. doi: 10.1186/s12935-022-02524-y.

Abstract

Cancer cells must rewire cellular metabolism to satisfy the unbridled proliferation, and metabolic reprogramming provides not only the advantage for cancer cell proliferation but also new targets for cancer treatment. However, the plasticity of the metabolic pathways makes them very difficult to target. Deubiquitylating enzymes (DUBs) are proteases that cleave ubiquitin from the substrate proteins and process ubiquitin precursors. While the molecular mechanisms are not fully understood, many DUBs have been shown to be involved in tumorigenesis and progression via controlling the dysregulated cancer metabolism, and consequently recognized as potential drug targets for cancer treatment. In this article, we summarized the significant progress in understanding the key roles of DUBs in cancer cell metabolic rewiring and the opportunities for the application of DUBs inhibitors in cancer treatment, intending to provide potential implications for both research purpose and clinical applications.

摘要

癌细胞必须重新调整细胞代谢以满足其不受控制的增殖需求,而代谢重编程不仅为癌细胞增殖提供了优势,也为癌症治疗提供了新的靶点。然而,代谢途径的可塑性使得它们很难成为靶点。去泛素化酶(DUBs)是一类蛋白酶,可从底物蛋白上切割泛素并加工泛素前体。尽管其分子机制尚未完全明确,但许多DUBs已被证明通过控制失调的癌症代谢参与肿瘤发生和进展,因此被视为癌症治疗的潜在药物靶点。在本文中,我们总结了在理解DUBs在癌细胞代谢重编程中的关键作用方面取得的重大进展,以及DUBs抑制剂在癌症治疗中的应用机会,旨在为研究目的和临床应用提供潜在启示。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed20/8935717/483f49dadf34/12935_2022_2524_Fig1_HTML.jpg

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