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肺腺癌中去泛素化酶的研究进展

Advances in deubiquitinating enzymes in lung adenocarcinoma.

作者信息

Zhou Xi-Jia, Li Rui, Liu Xiao, Qu Yi-Qing

机构信息

Department of Pulmonary and Critical Care Medicine, Qilu Hospital, Cheeloo College of Medicine, Shandong University (Jinan 250012, China).

Department of Pulmonary and Critical Care Medicine, Qilu Hospital of Shandong University (Jinan 250012, China).

出版信息

J Cancer. 2021 Jul 25;12(18):5573-5582. doi: 10.7150/jca.56532. eCollection 2021.

Abstract

The process of ubiquitination and deubiquitination is widely present in the human body's protein reactions and plays versatile roles in multiple diseases. Deubiquitinating enzymes (DUBs) are significant regulators of this process, which cleave the ubiquitin (Ub) moiety from various substrates and maintain protein stability. Lung adenocarcinoma (LUAD) is the most common type of non-small cell lung cancer (NSCLC) and remains refractory to treatment. To elucidate the mechanism of LUAD and advance new therapeutic targets, we review the latest research progress on DUBs in LUAD. We summarize the biological capabilities of these DUBs and further highlight those DUBs that may serve as anticancer target candidates for precision treatment. We also discuss deubiquitinase inhibitors, which are expected to play a role in targeted LUAD therapy.

摘要

泛素化和去泛素化过程广泛存在于人体蛋白质反应中,并在多种疾病中发挥多种作用。去泛素化酶(DUBs)是这一过程的重要调节因子,它能从各种底物上切割泛素(Ub)部分并维持蛋白质稳定性。肺腺癌(LUAD)是最常见的非小细胞肺癌(NSCLC)类型,且治疗仍然棘手。为阐明LUAD的发病机制并推进新的治疗靶点,我们综述了LUAD中DUBs的最新研究进展。我们总结了这些DUBs的生物学功能,并进一步强调了那些可能作为精准治疗抗癌靶点候选物的DUBs。我们还讨论了去泛素化酶抑制剂,其有望在LUAD靶向治疗中发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f71c/8364634/76d7065aa8de/jcav12p5573g001.jpg

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