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雌激素-自噬轴:对癌症和感染中细胞保护及治疗潜力的见解

The Estrogen-Autophagy Axis: Insights into Cytoprotection and Therapeutic Potential in Cancer and Infection.

作者信息

Zhao Ying, Klionsky Daniel J, Wang Xin, Huang Qiaoying, Deng Zixin, Xiang Jin

机构信息

Key Laboratory of Combinatorial Biosynthesis and Drug Discovery, Ministry of Education, School of Pharmaceutical Sciences, Wuhan University, Wuhan 430071, China.

Life Sciences Institute, University of Michigan, Mary Sue Coleman Hall, 210 Washtenaw Avenue, Ann Arbor, MI 48109-2216, USA.

出版信息

Int J Mol Sci. 2024 Nov 22;25(23):12576. doi: 10.3390/ijms252312576.

Abstract

Macroautophagy, commonly referred to as autophagy, is an essential cytoprotective mechanism that plays a significant role in cellular homeostasis. It has emerged as a promising target for drug development aimed at treating various cancers and infectious diseases. However, the scientific community has yet to reach a consensus on the most effective approach to manipulating autophagy, with ongoing debates about whether its inhibition or stimulation is preferable for managing these complex conditions. One critical factor contributing to the variability in treatment responses for both cancers and infectious diseases is estrogen, a hormone known for its diverse biological effects. Given the strong correlations observed between estrogen signaling and autophagy, this review seeks to summarize the intricate molecular mechanisms that underlie the dual cytoprotective effects of estrogen signaling in conjunction with autophagy. We highlight recent findings from studies that involve various ligands, disease contexts, and cell types, including immune cells. Furthermore, we discuss several factors that regulate autophagy in the context of estrogen's influence. Ultimately, we propose a hypothetical model to elucidate the regulatory effects of the estrogen-autophagy axis on cell fate. Understanding these interactions is crucial for advancing our knowledge of related diseases and facilitating the development of innovative treatment strategies.

摘要

巨自噬,通常简称为自噬,是一种重要的细胞保护机制,在细胞内稳态中发挥着重要作用。它已成为药物开发的一个有前景的靶点,旨在治疗各种癌症和传染病。然而,科学界尚未就操纵自噬的最有效方法达成共识,关于在管理这些复杂病症时抑制还是刺激自噬更可取,仍存在持续的争论。雌激素是一种以其多样生物学效应而闻名的激素,是导致癌症和传染病治疗反应差异的一个关键因素。鉴于雌激素信号传导与自噬之间存在密切关联,本综述旨在总结雌激素信号传导与自噬协同发挥双重细胞保护作用的复杂分子机制。我们重点介绍了涉及各种配体、疾病背景和细胞类型(包括免疫细胞)的研究的最新发现。此外,我们讨论了在雌激素影响下调节自噬的几个因素。最终,我们提出了一个假设模型来阐明雌激素 - 自噬轴对细胞命运的调节作用。了解这些相互作用对于推进我们对相关疾病的认识以及促进创新治疗策略的开发至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c308/11641569/6bb6e31e1d9b/ijms-25-12576-g001.jpg

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