Xiao Hao, Han Zeping, Xu Min, Gao Xukang, Qiu Shuangjian, Ren Ning, Yi Yong, Zhou Chenhao
Department of Liver Surgery and Transplantation, Zhongshan Hospital, Fudan University, Shanghai 200032, China.
Liver Cancer Institute, Zhongshan Hospital, Fudan University, Shanghai 200032, China.
Biomolecules. 2025 Apr 9;15(4):549. doi: 10.3390/biom15040549.
Necroptosis, a distinct form of regulated necrosis implicated in various human pathologies, is orchestrated through sophisticated signaling pathways. During this process, cells undergoing necroptosis exhibit characteristic necrotic morphology and provoke substantial inflammatory responses. Post-translational modifications (PTMs)-chemical alterations occurring after protein synthesis that critically regulate protein functionality-constitute essential regulatory components within these complex signaling cascades. This intricate crosstalk between necroptotic pathways and PTM networks presents promising therapeutic opportunities. Our comprehensive review systematically analyzes the molecular mechanisms underlying necroptosis, with particular emphasis on the regulatory roles of PTMs in signal transduction. Through systematic evaluation of key modifications including ubiquitination, phosphorylation, glycosylation, methylation, acetylation, disulfide bond formation, caspase cleavage, nitrosylation, and SUMOylation, we examine potential therapeutic applications targeting necroptosis in disease pathogenesis. Furthermore, we synthesize current pharmacological strategies for manipulating PTM-regulated necroptosis, offering novel perspectives on clinical target development and therapeutic intervention.
坏死性凋亡是一种与多种人类疾病相关的受调控坏死的独特形式,它通过复杂的信号通路进行调控。在此过程中,经历坏死性凋亡的细胞呈现出特征性的坏死形态,并引发大量炎症反应。翻译后修饰(PTMs)——蛋白质合成后发生的化学改变,对蛋白质功能起着关键调节作用——构成了这些复杂信号级联反应中的重要调控成分。坏死性凋亡途径与PTM网络之间这种复杂的相互作用提供了有前景的治疗机会。我们的全面综述系统地分析了坏死性凋亡的分子机制,特别强调了PTMs在信号转导中的调控作用。通过对包括泛素化、磷酸化、糖基化、甲基化、乙酰化、二硫键形成、半胱天冬酶切割、亚硝基化和SUMO化等关键修饰的系统评估,我们研究了针对疾病发病机制中坏死性凋亡的潜在治疗应用。此外,我们综合了当前操纵PTM调控的坏死性凋亡的药理学策略,为临床靶点开发和治疗干预提供了新的视角。