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增进对铁死亡的理解:分子机制、与细胞衰老的联系及对衰老的影响

Improving understanding of ferroptosis: Molecular mechanisms, connection with cellular senescence and implications for aging.

作者信息

De Leon-Oliva Diego, Boaru Diego Liviu, Minaya-Bravo Ana M, De Castro-Martinez Patricia, Fraile-Martinez Oscar, Garcia-Montero Cielo, Cobo-Prieto David, Barrena-Blázquez Silvestra, Lopez-Gonzalez Laura, Albillos Agustín, Alvarez-Mon Melchor, Saez Miguel A, Diaz-Pedrero Raul, Ortega Miguel A

机构信息

Department of Medicine and Medical Specialities, (CIBERehd), Faculty of Medicine and Health Sciences, University of Alcalá, 28801, Alcala de Henares, Spain.

Ramón y Cajal Institute of Sanitary Research (IRYCIS), 28034, Madrid, Spain.

出版信息

Heliyon. 2024 Oct 24;10(21):e39684. doi: 10.1016/j.heliyon.2024.e39684. eCollection 2024 Nov 15.


DOI:10.1016/j.heliyon.2024.e39684
PMID:39553553
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11564042/
Abstract

In the face of cell damage, cells can initiate a response ranging from survival to death, the balance being crucial for tissue homeostasis and overall health. Cell death, in both accidental and regulated forms, plays a fundamental role in maintaining tissue homeostasis. Among the regulated mechanisms of cell death, ferroptosis has garnered attention for its iron-dependent phospholipid (PL) peroxidation and its implications in aging and age-related disorders, as well as for its therapeutic relevance. In this review, we provide an overview of the mechanisms, regulation, and physiological and pathological roles of ferroptosis. We present new insights into the relationship between ferroptosis, cellular senescence and aging, emphasizing how alterations in ferroptosis pathways contribute to aging-related tissue dysfunction. In addition, we examine the therapeutic potential of ferroptosis in aging-related diseases, offering innovative insights into future interventions aimed at mitigating the effects of aging and promoting longevity.

摘要

面对细胞损伤时,细胞能够启动从存活到死亡的一系列反应,这种平衡对于组织稳态和整体健康至关重要。细胞死亡,无论是意外形式还是调控形式,在维持组织稳态中都起着基础性作用。在细胞死亡的调控机制中,铁死亡因其铁依赖性磷脂(PL)过氧化作用、在衰老及与年龄相关疾病中的影响以及治疗相关性而受到关注。在本综述中,我们概述了铁死亡的机制、调控以及生理和病理作用。我们对铁死亡、细胞衰老和衰老之间的关系提出了新见解,强调了铁死亡途径的改变如何导致与衰老相关的组织功能障碍。此外,我们研究了铁死亡在与衰老相关疾病中的治疗潜力,为旨在减轻衰老影响和促进长寿的未来干预措施提供了创新性见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e872/11564042/aafdfde18451/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e872/11564042/96e93ba72014/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e872/11564042/26e68b6dfee4/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e872/11564042/aafdfde18451/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e872/11564042/96e93ba72014/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e872/11564042/26e68b6dfee4/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e872/11564042/aafdfde18451/gr3.jpg

相似文献

[1]
Improving understanding of ferroptosis: Molecular mechanisms, connection with cellular senescence and implications for aging.

Heliyon. 2024-10-24

[2]
Sterols in ferroptosis: from molecular mechanisms to therapeutic strategies.

Trends Mol Med. 2025-1

[3]
Platelet-derived exosomes alleviate tendon stem/progenitor cell senescence and ferroptosis by regulating AMPK/Nrf2/GPX4 signaling and improve tendon-bone junction regeneration in rats.

J Orthop Surg Res. 2024-6-28

[4]
Ferroptosis and Senescence: A Systematic Review.

Int J Mol Sci. 2023-2-11

[5]
Ferroptosis in Cardiovascular Disease and Cardiomyopathies: Therapeutic Implications of Glutathione and Iron Chelating Agents.

Biomedicines. 2024-3-1

[6]
Peroxisomal homeostasis in metabolic diseases and its implication in ferroptosis.

Cell Commun Signal. 2024-10-4

[7]
Lipid Peroxidation and Iron Metabolism: Two Corner Stones in the Homeostasis Control of Ferroptosis.

Int J Mol Sci. 2022-12-27

[8]
Molecular mechanisms of ferroptosis and relevance to inflammation.

Inflamm Res. 2023-2

[9]
Iron Accumulation and Lipid Peroxidation in the Aging Retina: Implication of Ferroptosis in Age-Related Macular Degeneration.

Aging Dis. 2021-4-1

[10]
Macrophage iron dyshomeostasis promotes aging-related renal fibrosis.

Aging Cell. 2024-11

引用本文的文献

[1]
Exploring the synergetic role of cuproptosis and ferroptosis and their implication in advancing cancer therapeutics.

Discov Oncol. 2025-7-8

[2]
Bioinformatics-Guided Experimental Validation Identifies NQO1 as a Senescence-Ferroptosis Hub in Liver Fibrosis.

Biomedicines. 2025-5-20

本文引用的文献

[1]
Cryptochrome 1 regulates ovarian granulosa cell senescence through NCOA4-mediated ferritinophagy.

Free Radic Biol Med. 2024-5-1

[2]
Connecting epigenetics and inflammation in vascular senescence: state of the art, biomarkers and senotherapeutics.

Front Genet. 2024-2-26

[3]
Ferroptosis in cancer: From molecular mechanisms to therapeutic strategies.

Signal Transduct Target Ther. 2024-3-8

[4]
Dihydroartemisinin eliminates senescent cells by promoting autophagy-dependent ferroptosis via AMPK/mTOR signaling pathway.

Cell Biol Int. 2024-5

[5]
Ferroptosis in age-related vascular diseases: Molecular mechanisms and innovative therapeutic strategies.

Biomed Pharmacother. 2024-4

[6]
NINJ1 induces plasma membrane rupture and release of damage-associated molecular pattern molecules during ferroptosis.

EMBO J. 2024-4

[7]
Progress of Ferroptosis in Ischemic Stroke and Therapeutic Targets.

Cell Mol Neurobiol. 2024-2-23

[8]
Targeted Liposomes Sensitize Plastic Melanoma to Ferroptosis via Senescence Induction and Coenzyme Depletion.

ACS Nano. 2024-3-5

[9]
Ferroptosis as a potential therapeutic target for age-related macular degeneration.

Drug Discov Today. 2024-4

[10]
The cell biology of ferroptosis.

Nat Rev Mol Cell Biol. 2024-6

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