Mechanisms of Bellidifolin in Treating Doxorubicin-Induced Cardiotoxicity: Network Pharmacology, Molecular Docking, and Experimental Verification

BEL presents as a promising therapeutic candidate for cardiotoxicity, likely through its anti-fibrotic effects via the reduction of TGF-β1, α-SMA, Col I, and Col III expression, alongside regulation in the PI3K-AKT signaling pathway.

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Publication Details

Journal
Frontiers in Bioscience-Landmark
Published
2026-01-21
DOI
https://doi.org/10.31083/fbl47028
Primary Topic
Chemotherapy-induced cardiotoxicity and mitigation
Type
article
Field-Weighted Citation Impact
0.00
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article

Mechanisms of Bellidifolin in Treating Doxorubicin-Induced Cardiotoxicity: Network Pharmacology, Molecular Docking, and Experimental Verification

Aiying Li, Fan Gao, Jiangli Wu, Yu Liu et al.
Frontiers in Bioscience-Landmark
Chemotherapy-induced cardiotoxicity and mitigation
article

Mechanisms of Bellidifolin in Treating Doxorubicin-Induced Cardiotoxicity: Network Pharmacology, Molecular Docking, and Experimental Verification

Aiying Li, Fan Gao, Jiangli Wu, Yu Liu, Zhenyang Zhong, Yalei Liu, Cheng Dai, Xinmeng Zhao
article en

Abstract

BEL presents as a promising therapeutic candidate for cardiotoxicity, likely through its anti-fibrotic effects via the reduction of TGF-β1, α-SMA, Col I, and Col III expression, alongside regulation in the PI3K-AKT signaling pathway.

Frontiers in Bioscience-LandmarkVol. 31(1)
Hebei University of Chinese Medicine (CN), Hebei Science and Technology Department (CN), Hebei Institute of Physical Education (CN)
Good health and well-being
Openalex Percentile: Top 74%
Chemotherapy-induced cardiotoxicity and mitigation
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Mechanisms of Bellidifolin in Treating Doxorubicin-Induced Cardiotoxicity: Network Pharmacology, Molecular Docking, and Experimental Verification — Aiying Li, Fan Gao, et al. · Frontiers in Bioscience-Landmark (2026) | TGRS Research Map | TGRS