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MALT1抑制剂与降解剂:针对NF-κB驱动的恶性肿瘤的策略

MALT1 Inhibitors and Degraders: Strategies for NF-κB-Driven Malignancies.

作者信息

Zhang Ru-Yue, Wang Zi-Xuan, Zhang Meng-Yuan, Wang Yu-Fan, Zhou Si-Li, Xu Jia-Lu, Lin Wen-Xuan, Ji Tian-Rui, Chen Ya-Dong, Lu Tao, Li Nian-Guang, Shi Zhi-Hao

机构信息

Laboratory of Molecular Design and Drug Discovery, School of Science, China Pharmaceutical University, 639 Longmian Avenue, Nanjing, Jiangsu 211198, China.

National and Local Collaborative Engineering Center of Chinese Medicinal Resources Industrialization and Formulae Innovative Medicine, Nanjing University of Chinese Medicine, 138 Xianlin Road, Nanjing, Jiangsu 210023, China.

出版信息

J Med Chem. 2025 Mar 13;68(5):5075-5096. doi: 10.1021/acs.jmedchem.4c02873. Epub 2025 Feb 25.

Abstract

Mucosa-associated lymphoid tissue protein 1 (MALT1), a cysteine protease and the sole paracaspase in humans, plays a pivotal role in the survival and proliferation of NF-κB-dependent malignant cancers, particularly MALT lymphoma and diffuse large B-cell lymphoma (DLBCL). Dysregulated MALT1 activity is implicated in various malignancies, highlighting its importance as a therapeutic target. This Perspective provides an overview of MALT1's structural and functional characteristics, summarizes recent advancements in small-molecule inhibitors and degraders targeting this protein, and discusses compound structures, structure-activity relationship (SAR) analyses, and biological activities. We aim to inform future research efforts to enhance the activity, selectivity, and pharmacological properties of MALT1-targeting compounds, establishing a foundational framework for drug development in this critical area of cancer therapy.

摘要

黏膜相关淋巴组织蛋白1(MALT1)是一种半胱氨酸蛋白酶,也是人类唯一的旁胱天蛋白酶,在NF-κB依赖性恶性肿瘤(尤其是MALT淋巴瘤和弥漫性大B细胞淋巴瘤(DLBCL))的存活和增殖中起关键作用。MALT1活性失调与多种恶性肿瘤有关,凸显了其作为治疗靶点的重要性。本综述概述了MALT1的结构和功能特征,总结了靶向该蛋白的小分子抑制剂和降解剂的最新进展,并讨论了化合物结构、构效关系(SAR)分析和生物学活性。我们旨在为未来的研究工作提供信息,以提高靶向MALT1化合物的活性、选择性和药理特性,为这一癌症治疗关键领域的药物开发建立基础框架。

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