Serinc2-STAT3 protects against doxorubicin-induced cardiotoxicity via promoting mitochondrial bioenergetics

Taken together, it can be concluded that Serinc2 can maintain mitochondrial dynamics and increase mitochondrial bioenergy generation by enhancing STAT3 phosphorylation activity, thereby alleviating oxidative stress, apoptotic responses, and improving doxorubicin-induced cardiac dysfunction.

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Publication Details

Journal
Redox Biology
Published
2026-01-22
DOI
https://doi.org/10.1016/j.redox.2026.104045
Citations
1
Primary Topic
Chemotherapy-induced cardiotoxicity and mitigation
Type
article
Field-Weighted Citation Impact
30.07
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article

Serinc2-STAT3 protects against doxorubicin-induced cardiotoxicity via promoting mitochondrial bioenergetics

Mian Cheng, Saeed Kashkooli, Zheyu Liu, Tao Liu et al.
1 citations
Redox Biology
Chemotherapy-induced cardiotoxicity and mitigation
30.07
article

Serinc2-STAT3 protects against doxorubicin-induced cardiotoxicity via promoting mitochondrial bioenergetics

Mian Cheng, Saeed Kashkooli, Zheyu Liu, Tao Liu, Min Huang, Shan Hu, Gang Wu, Hao Ju, Manqi Yang
article en
1 citations

Abstract

Taken together, it can be concluded that Serinc2 can maintain mitochondrial dynamics and increase mitochondrial bioenergy generation by enhancing STAT3 phosphorylation activity, thereby alleviating oxidative stress, apoptotic responses, and improving doxorubicin-induced cardiac dysfunction.

Redox BiologyVol. 90
Shanghai Chest Hospital (CN), Wuhan University (CN), Tongren Hospital (CN), Zhongnan Hospital of Wuhan University (CN), Renmin Hospital of Wuhan University (CN), Tongji Hospital (CN), Huazhong University of Science and Technology (CN)
Openalex Percentile: Top 2%
Chemotherapy-induced cardiotoxicity and mitigation
30.07
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