The interplay of p38 MAPK signaling and mitochondrial metabolism, a dynamic target in cancer and pathological contexts

线粒体 细胞生物学 线粒体生物发生 生物 MAPK/ERK通路 信号转导 蛋白激酶A 氧化应激 生物能学 自噬 氧化磷酸化 p38丝裂原活化蛋白激酶 激酶 生物化学 细胞凋亡
作者
Nadin H. Sarg,Dana M. Zaher,Nour N. Abu Jayab,Salma Mostafa,Hussein H. Ismail,Hany A. Omar
出处
期刊:Biochemical Pharmacology [Elsevier BV]
卷期号:225: 116307-116307 被引量:6
标识
DOI:10.1016/j.bcp.2024.116307
摘要

Mitochondria play a crucial role in cellular metabolism and bioenergetics, orchestrating various cellular processes, including energy production, metabolism, adaptation to stress, and redox balance. Besides, mitochondria regulate cellular metabolic homeostasis through coordination with multiple signaling pathways. Importantly, the p38 mitogen-activated protein kinase (MAPK) signaling pathway is a key player in the intricate communication with mitochondria, influencing various functions. This review explores the multifaced interaction between the mitochondria and p38 MAPK signaling and the consequent impact on metabolic alterations. Overall, the p38 MAPK pathway governs the activities of key mitochondrial proteins, which are involved in mitochondrial biogenesis, oxidative phosphorylation, thermogenesis, and iron homeostasis. Additionally, p38 MAPK contributes to the regulation of mitochondrial responses to oxidative stress and apoptosis induced by cancer therapies or natural substances by coordinating with other pathways responsible for energy homeostasis. Therefore, dysregulation of these interconnected pathways can lead to various pathologies characterized by aberrant metabolism. Consequently, gaining a deeper understanding of the interaction between mitochondria and the p38 MAPK pathway and their implications presents exciting forecasts for novel therapeutic interventions in cancer and other disorders characterized by metabolic dysregulation.
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