Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2025 Oct;33(5):1538-1541.
doi: 10.19746/j.cnki.issn.1009-2137.2025.05.044.

[The mechanism of Ferroptosis in Aplastic Anemia --Review]

[Article in Chinese]
Affiliations
Review

[The mechanism of Ferroptosis in Aplastic Anemia --Review]

[Article in Chinese]
Yu-Jie Qin et al. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2025 Oct.

Abstract

Ferroptosis initiates membrane oxidative damage through lipid peroxidation and iron accumulation, and accumulates reactive oxygen species (ROS) during aplastic anemia (AA). Ferroptosis induces damage and apoptosis of hematopoietic stem/progenitor cells, mesenchymal stem cells, blood cells, and T lymphocytes through various pathways, inhibits bone marrow hematopoiesis, damages bone marrow microenvironment, exacerbates immune imbalance, leading to bone marrow failure and disease progression. Therefore, further exploring the ferroptosis mechanism in AA can help clarify the pathogenesis of disease and provide new research ideas and directions for the treatment of AA.

题目: 铁死亡在再生障碍性贫血中的作用机制.

摘要: 在再生障碍性贫血病程中,铁死亡通过脂质过氧化和铁积累启动膜氧化损伤,积累活性氧,并通过多种途径诱导造血干/祖细胞、间充质干细胞、血细胞和T淋巴细胞损伤和凋亡,抑制骨髓造血、破坏骨髓微环境、加剧免疫失衡,导致骨髓造血功能衰竭,疾病进展。进一步深入探讨铁死亡机制在再生障碍性贫血中的作用,有助于阐明疾病发病机理,为治疗再生障碍性贫血提供新的研究思路和方向。.

Keywords: aplastic anemia; ferroptosis; oxidative stress; mechanism.

PubMed Disclaimer

Substances

LinkOut - more resources