Irisin Mitigates Doxorubicin-Induced Cardiotoxicity by Reducing Oxidative Stress and Inflammation via Modulation of the PERK-eIF2α-ATF4 Pathway

Irisin mitigates oxidative stress and inflammation by modulating the PERK-eIF2α-ATF4 pathway, highlighting its potential as a prospective approach for combating DOX-induced cardiotoxicity.

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Publication Details

Journal
Drug Design Development and Therapy
Published
2025-02-01
DOI
https://doi.org/10.2147/dddt.s492691
Citations
7
Primary Topic
Chemotherapy-induced cardiotoxicity and mitigation
Type
article
Field-Weighted Citation Impact
9.72
Controls
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article

Irisin Mitigates Doxorubicin-Induced Cardiotoxicity by Reducing Oxidative Stress and Inflammation via Modulation of the PERK-eIF2α-ATF4 Pathway

Yongguo Liu, Wenbo Fu, Xiaolin Yu, Xiangyu Dong et al.
7 citations
Drug Design Development and Therapy
Chemotherapy-induced cardiotoxicity and mitigation
9.72
article

Irisin Mitigates Doxorubicin-Induced Cardiotoxicity by Reducing Oxidative Stress and Inflammation via Modulation of the PERK-eIF2α-ATF4 Pathway

Yongguo Liu, Wenbo Fu, Xiaolin Yu, Xiangyu Dong, Zilong Zhang, Jie Li, Zhao Wang, Xin Shen
article en
7 citations

Abstract

Irisin mitigates oxidative stress and inflammation by modulating the PERK-eIF2α-ATF4 pathway, highlighting its potential as a prospective approach for combating DOX-induced cardiotoxicity.

Drug Design Development and TherapyVol. Volume 19
People's Hospital of Xinjiang Uygur Autonomous Region (CN)
Openalex Percentile: Top 2%
Chemotherapy-induced cardiotoxicity and mitigation
9.72
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