Discovery of benzethonium chloride as a potent STAT3 inhibitor for the treatment of HNSCC

Head and neck squamous cell carcinoma (HNSCC) is a prevalent malignancy with high mortality, and effective treatment strategies remain limited. This study investigated the effects of benzethonium chloride (BZN), an FDA-approved anti-infective agent, on HNSCC cell lines and its underlying mechanisms. BZN significantly inhibited the proliferation of HNSCC cell lines CAL27 and FaDu and induced apoptosis in both cell lines <i>in vitro</i>. In a subcutaneous tumor model, BZN markedly suppressed tumor growth in the mouse HNSCC cell line MOC1. Mechanistically, BZN may directly bind to the SH2 domain of STAT3, inhibit its dimerization, prevent the nuclear translocation of phosphorylated STAT3 (p-STAT3), downregulate the expression of the downstream protein MCL-1, and induce mitochondrial-mediated apoptosis in FaDu and CAL27 cells. These findings highlight BZN as a potential therapeutic agent for HNSCC, offering a novel approach to improve treatment outcomes in clinical settings.

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Publication Details

Journal
Frontiers in Pharmacology
Published
2025-04-02
DOI
https://doi.org/10.3389/fphar.2025.1569570
Primary Topic
Cytokine Signaling Pathways and Interactions
Type
article
Field-Weighted Citation Impact
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article

Discovery of benzethonium chloride as a potent STAT3 inhibitor for the treatment of HNSCC

Deshang Chen, Mingyang Deng, Bao Zhao, Guoying Han et al.
Frontiers in Pharmacology
Cytokine Signaling Pathways and Interactions
article

Discovery of benzethonium chloride as a potent STAT3 inhibitor for the treatment of HNSCC

Deshang Chen, Mingyang Deng, Bao Zhao, Guoying Han, Xianming Ge, Qianqian Xu, Beibei Xu, Mingjie Zhang, Shumin Li, Mengli Wang, Yan Pan, Yuefeng Han, Sien Ma
article en

Abstract

Head and neck squamous cell carcinoma (HNSCC) is a prevalent malignancy with high mortality, and effective treatment strategies remain limited. This study investigated the effects of benzethonium chloride (BZN), an FDA-approved anti-infective agent, on HNSCC cell lines and its underlying mechanisms. BZN significantly inhibited the proliferation of HNSCC cell lines CAL27 and FaDu and induced apoptosis in both cell lines <i>in vitro</i>. In a subcutaneous tumor model, BZN markedly suppressed tumor growth in the mouse HNSCC cell line MOC1. Mechanistically, BZN may directly bind to the SH2 domain of STAT3, inhibit its dimerization, prevent the nuclear translocation of phosphorylated STAT3 (p-STAT3), downregulate the expression of the downstream protein MCL-1, and induce mitochondrial-mediated apoptosis in FaDu and CAL27 cells. These findings highlight BZN as a potential therapeutic agent for HNSCC, offering a novel approach to improve treatment outcomes in clinical settings.

Frontiers in PharmacologyVol. 16
Hefei University of Technology (CN), Bengbu Medical College (CN), First Affiliated Hospital of Bengbu Medical College (CN)
Openalex Percentile: Top 91%
Cytokine Signaling Pathways and Interactions
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