Overview of pyroptosis mechanism and in-depth analysis of cardiomyocyte pyroptosis mediated by NF-κB pathway in heart failure

IF 6.9 2区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL Biomedicine & Pharmacotherapy Pub Date : 2024-08-29 DOI:10.1016/j.biopha.2024.117367
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Abstract

The pyroptosis of cardiomyocytes has become an essential topic in heart failure research. The abnormal accumulation of these biological factors, including angiotensin II, advanced glycation end products, and various growth factors (such as connective tissue growth factor, vascular endothelial growth factor, transforming growth factor beta, among others), activates the nuclear factor-κB (NF-κB) signaling pathway in cardiovascular diseases, ultimately leading to pyroptosis of cardiomyocytes. Therefore, exploring the underlying molecular biological mechanisms is essential for developing novel drugs and therapeutic strategies. However, our current understanding of the precise regulatory mechanism of this complex signaling pathway in cardiomyocyte pyroptosis is still limited. Given this, this study reviews the milestone discoveries in the field of pyroptosis research since 1986, analyzes in detail the similarities, differences, and interactions between pyroptosis and other cell death modes (such as apoptosis, necroptosis, autophagy, and ferroptosis), and explores the deep connection between pyroptosis and heart failure. At the same time, it depicts in detail the complete pathway of the activation, transmission, and eventual cardiomyocyte pyroptosis of the NF-κB signaling pathway in the process of heart failure. In addition, the study also systematically summarizes various therapeutic approaches that can inhibit NF-κB to reduce cardiomyocyte pyroptosis, including drugs, natural compounds, small molecule inhibitors, gene editing, and other cutting-edge technologies, aiming to provide solid scientific support and new research perspectives for the prevention and treatment of heart failure.

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心力衰竭中 NF-κB 通路介导的心肌细胞热解机制概述和深入分析
心肌细胞的热解已成为心力衰竭研究的一个重要课题。在心血管疾病中,血管紧张素 II、高级糖化终产物和各种生长因子(如结缔组织生长因子、血管内皮生长因子、转化生长因子 beta 等)等生物因子的异常积累激活了核因子-κB(NF-κB)信号通路,最终导致心肌细胞的热解。因此,探索潜在的分子生物学机制对于开发新型药物和治疗策略至关重要。然而,目前我们对心肌细胞热解过程中这一复杂信号通路的精确调控机制的了解仍然有限。有鉴于此,本研究回顾了自 1986 年以来热凋亡研究领域的里程碑式发现,详细分析了热凋亡与其他细胞死亡模式(如细胞凋亡、坏死、自噬和铁凋亡)之间的异同和相互作用,并探讨了热凋亡与心力衰竭之间的深层联系。同时,它详细描绘了心衰过程中 NF-κB 信号通路激活、传递并最终导致心肌细胞热解的完整路径。此外,该研究还系统地总结了抑制NF-κB以减少心肌细胞凋亡的各种治疗方法,包括药物、天然化合物、小分子抑制剂、基因编辑等前沿技术,旨在为心衰的预防和治疗提供坚实的科学依据和新的研究视角。
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来源期刊
CiteScore
11.90
自引率
2.70%
发文量
1621
审稿时长
48 days
期刊介绍: Biomedicine & Pharmacotherapy stands as a multidisciplinary journal, presenting a spectrum of original research reports, reviews, and communications in the realms of clinical and basic medicine, as well as pharmacology. The journal spans various fields, including Cancer, Nutriceutics, Neurodegenerative, Cardiac, and Infectious Diseases.
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