The therapeutic effect and specific mechanism involved active Chinese medicine component biochaninA in glioma

Introduction: Glioma is a common primary solid brain tumor with high incidence and poor prognosis. Biochanin A (bioA), an active component of traditional Chinese medicine, has potential therapeutic effects on it, but its mechanism remains unclear. This study aimed to clarify its mechanism via a multi-omics strategy. Methods: A multi-omics integration approach was adopted, which combined single-cell RNA sequencing, in vitro experiments, the construction of a Glutathione S-transferase P1 (GSTP1)-based prognostic model, and analyses of immune infiltration and drug sensitivity to evaluate its clinical value. Results: C2 CENPF⁺ tumor cells were specifically expressed in recurrent gliomas and associated with the bioA pathway. GSTP1 was the key target gene of bioA; its high expression was related to poor prognosis, and its knockout could inhibit glioma progression. The GSTP1-based prognostic model had excellent predictive efficiency. Discussion: BioA may exert anti-glioma effects by regulating GSTP1, providing theoretical support for its clinical application and a new therapeutic target for glioma.

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Publication Details

Journal
Frontiers in Immunology
Published
2026-04-21
DOI
https://doi.org/10.3389/fimmu.2026.1780159
Primary Topic
Ferroptosis and cancer prognosis
Type
article
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The therapeutic effect and specific mechanism involved active Chinese medicine component biochaninA in glioma

Desong Kong, Changqing Wang, Dan Chai, Yujie Zhu et al.
Frontiers in Immunology
Ferroptosis and cancer prognosis
article

The therapeutic effect and specific mechanism involved active Chinese medicine component biochaninA in glioma

Desong Kong, Changqing Wang, Dan Chai, Yujie Zhu, Lei Sun, Mengran Xi, J Y Zhang, Lu Gao, Xinru Xiao, Qiang Cai
article en

Abstract

Introduction: Glioma is a common primary solid brain tumor with high incidence and poor prognosis. Biochanin A (bioA), an active component of traditional Chinese medicine, has potential therapeutic effects on it, but its mechanism remains unclear. This study aimed to clarify its mechanism via a multi-omics strategy. Methods: A multi-omics integration approach was adopted, which combined single-cell RNA sequencing, in vitro experiments, the construction of a Glutathione S-transferase P1 (GSTP1)-based prognostic model, and analyses of immune infiltration and drug sensitivity to evaluate its clinical value. Results: C2 CENPF⁺ tumor cells were specifically expressed in recurrent gliomas and associated with the bioA pathway. GSTP1 was the key target gene of bioA; its high expression was related to poor prognosis, and its knockout could inhibit glioma progression. The GSTP1-based prognostic model had excellent predictive efficiency. Discussion: BioA may exert anti-glioma effects by regulating GSTP1, providing theoretical support for its clinical application and a new therapeutic target for glioma.

Frontiers in ImmunologyVol. 17
Nanjing University of Chinese Medicine (CN), Shandong University of Traditional Chinese Medicine (CN), Capital Medical University (CN), Anhui Medical University (CN), Fudan University (CN), First Affiliated Hospital of Anhui Medical University (CN)
No poverty
Openalex Percentile: Top 21%
Ferroptosis and cancer prognosis
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