# Bavachin suppresses proliferation of laryngopharyngeal cancer by regulating the STAT3 and MAPK signaling pathways

**Authors:** Xiaonan Yang, Zhimin Ding, Hongting Hua, Ruijia Gan, Dongdong Meng, Yan Zang, Han Xiao, Dong Wang, Wanjin Jiang, Dongyu Si, Xiang Wei, Mei Zhang, Huabing Zhang, Chaobing Gao

PMC · DOI: 10.7150/jca.92956 · Journal of Cancer · 2025-03-31

## TL;DR

Bavachin, a compound, was found to reduce the growth of laryngopharyngeal cancer cells by affecting key signaling pathways and promoting cell death.

## Contribution

This study reveals bavachin's antitumor effects on laryngopharyngeal cancer via modulation of STAT3 and MAPK pathways.

## Key findings

- Bavachin suppresses cancer cell proliferation and migration in vitro and in vivo.
- Bavachin induces apoptosis and cell cycle arrest by altering Bax, Bcl-2, CDK4/6, and CyclinD1 levels.
- Bavachin promotes ferroptosis by reducing GPX4 and increasing ROS and GSH.

## Abstract

Purpose: The present study aimed to explore the underlying antitumor effects of bavachin on laryngopharyngeal cancer in-vitro and in-vivo.

Methods: Tu212 and FaDu cells were cultured in the incubator. Cells were treated with 0.1% DMSO (control group) and different concentrations of bavachin (experimental groups) for exploring the results of proliferation and apoptosis. We revealed the underlying mechanism of bavachin on laryngopharyngeal cancer through western blotting, qRT-PCR assay and immunofluorescence staining.

Results: Bavachin could suppress the proliferation and migration of laryngopharyngeal cancer cells in-vitro and in-vivo. Mechanistically, the results suggested that bavachin could downregulate the phosphorylation level of the signal transducer and activator of the transcription 3 (STAT3) and upregulate those of the mitogen-activated protein kinase (MAPK). Furthermore, bavachin also increased the expression level of Bax and suppressed those of Bcl-2, CDK4/6, and CyclinD1 in the laryngopharyngeal cancer cells. Additionally, the study also identified that bavachin promoted ferroptosis by decreasing the expression level of glutathione peroxidase 4 (GPX4) and increasing those of intracellular reactive oxygen species (ROS) and glutathione (GSH).

Conclusion: Taken together, these results demonstrated that bavachin could suppress the growth and migration of laryngopharyngeal cancer cells and induce apoptosis and cell cycle arrest of the laryngopharyngeal cancer cells by regulating the MAPK/STAT3 signaling pathway. This study demonstrated that bavachin exhibited a clinical therapeutic potential for laryngopharyngeal cancer.

## Linked entities

- **Genes:** STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774], MAPK (mitogen activated kinase-like protein) [NCBI Gene 7446652], BAX (BCL2 associated X, apoptosis regulator) [NCBI Gene 581], BCL2 (BCL2 apoptosis regulator) [NCBI Gene 596], CDK4 (cyclin dependent kinase 4) [NCBI Gene 1019], CDK6 (cyclin dependent kinase 6) [NCBI Gene 1021], ccnd1.S (cyclin D1 S homeolog) [NCBI Gene 379161], GPX4 (glutathione peroxidase 4) [NCBI Gene 2879]
- **Chemicals:** bavachin (PubChem CID 14236566), DMSO (PubChem CID 679)

## Full-text entities

- **Genes:** STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774] {aka ADMIO, ADMIO1, APRF, HIES}, GPX4 (glutathione peroxidase 4) [NCBI Gene 2879] {aka GPx-4, GSHPx-4, MCSP, PHGPx, SMDS, snGPx}, BAX (BCL2 associated X, apoptosis regulator) [NCBI Gene 581] {aka BCL2L4}, BCL2 (BCL2 apoptosis regulator) [NCBI Gene 596] {aka Bcl-2, PPP1R50}, CCND1 (cyclin D1) [NCBI Gene 595] {aka BCL1, D11S287E, PRAD1, U21B31}
- **Diseases:** laryngopharyngeal cancer (MESH:D009369)
- **Cell lines:** FaDu — Homo sapiens (Human), Hypopharyngeal squamous cell carcinoma, Cancer cell line (CVCL_1218), Tu212 — Homo sapiens (Human), Head and neck squamous cell carcinoma, Cancer cell line (CVCL_4915)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12036085/full.md

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12036085/full.md

## References

44 references — full list in the complete paper: https://tomesphere.com/paper/PMC12036085/full.md

---
Source: https://tomesphere.com/paper/PMC12036085