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解析 AKT/ERK 级联及其在帕金森病中的作用。

Unraveling the AKT/ERK cascade and its role in Parkinson disease.

机构信息

Department of Biochemistry, Institute of Science, Banaras Hindu University, Varanasi, 221005, Uttar Pradesh, India.

出版信息

Arch Toxicol. 2024 Oct;98(10):3169-3190. doi: 10.1007/s00204-024-03829-9. Epub 2024 Aug 13.

Abstract

Parkinson disease represents a significant and growing burden on global healthcare systems, necessitating a deeper understanding of their underlying molecular mechanisms for the development of effective treatments. The AKT and ERK pathways play crucial roles in the disease, influencing multiple cellular pathways that support neuronal survival. Researchers have made notable progress in uncovering how these pathways are controlled by upstream kinases and how their downstream effects contribute to cell signalling. However, as we delve deeper into their intricacies, we encounter increasing complexity, compounded by the convergence of multiple signalling pathways. Many of their targets overlap with those of other kinases, and they not only affect specific substrates but also influence entire signalling networks. This review explores the intricate interplay of the AKT/ERK pathways with several other signalling cascades, including oxidative stress, endoplasmic reticulum stress, calcium homeostasis, inflammation, and autophagy, in the context of Parkinson disease. We discuss how dysregulation of these pathways contributes to disease progression and neuronal dysfunction, highlighting potential therapeutic targets for intervention. By elucidating the complex network of interactions between the AKT/ERK pathways and other signalling cascades, this review aims to provide insights into the pathogenesis of Parkinson disease and describe the development of novel therapeutic strategies.

摘要

帕金森病代表着全球医疗保健系统的重大且日益增长的负担,因此需要更深入地了解其潜在的分子机制,以开发有效的治疗方法。AKT 和 ERK 途径在该疾病中发挥着关键作用,影响支持神经元存活的多个细胞途径。研究人员在揭示这些途径如何被上游激酶控制以及它们的下游效应如何促进细胞信号传递方面取得了显著进展。然而,当我们更深入地研究它们的复杂性时,我们会遇到越来越多的复杂性,这是由多个信号通路的汇聚造成的。它们的许多靶点与其他激酶的靶点重叠,它们不仅影响特定的底物,还影响整个信号网络。这篇综述探讨了 AKT/ERK 途径与其他几种信号级联(包括氧化应激、内质网应激、钙稳态、炎症和自噬)在帕金森病中的错综复杂的相互作用。我们讨论了这些途径的失调如何导致疾病进展和神经元功能障碍,强调了干预的潜在治疗靶点。通过阐明 AKT/ERK 途径与其他信号级联之间的复杂相互作用网络,本综述旨在深入了解帕金森病的发病机制,并描述新的治疗策略的发展。

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