Brusatol Regulates Ferroptosis of Ovarian Cancer Through the Nrf2/HO-1/NQO1 and AKT/mTOR Double Signaling Pathways

In this study, we demonstrated for the first time through bioinformatics, molecular docking technology, and experimental validation that BRU acts as a novel inducer of ferroptosis in ovarian cancer cells by targeting the Nrf2/HO-1/NQO1 and AKT/mTOR dual signaling pathways, and may have great potential in the treatment of ovarian cancer cells.

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Publication Details

Journal
Current Pharmaceutical Design
Published
2025-08-22
DOI
https://doi.org/10.2174/0113816128383328250808123933
Citations
2
Primary Topic
Cancer, Lipids, and Metabolism
Type
article
Field-Weighted Citation Impact
1.87
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article

Brusatol Regulates Ferroptosis of Ovarian Cancer Through the Nrf2/HO-1/NQO1 and AKT/mTOR Double Signaling Pathways

Jian Hua, Chaoqun Lian, XIAOFU LIAN, Hongli Liu et al.
2 citations
Current Pharmaceutical Design
Cancer, Lipids, and Metabolism
1.87
article

Brusatol Regulates Ferroptosis of Ovarian Cancer Through the Nrf2/HO-1/NQO1 and AKT/mTOR Double Signaling Pathways

Jian Hua, Chaoqun Lian, XIAOFU LIAN, Hongli Liu, Luyao Wang, Jing Zhang, Mengling Hu
article en
2 citations

Abstract

In this study, we demonstrated for the first time through bioinformatics, molecular docking technology, and experimental validation that BRU acts as a novel inducer of ferroptosis in ovarian cancer cells by targeting the Nrf2/HO-1/NQO1 and AKT/mTOR dual signaling pathways, and may have great potential in the treatment of ovarian cancer cells.

Current Pharmaceutical DesignVol. 32(17)
Bengbu Medical College (CN), First Affiliated Hospital of Bengbu Medical College (CN)
Openalex Percentile: Top 13%
Cancer, Lipids, and Metabolism
1.87
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