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A comprehensive review of Schisandrin B’s preclinical antitumor activity and mechanistic insights from network pharmacology

Affiliation
The Key Laboratory of biomarker high throughput screening and target translation of breast and gastrointestinal tumor ,Affiliated Zhongshan Hospital of Dalian University ,Dalian ,Liaoning ,China
Fang, Yanhua;
Affiliation
The Key Laboratory of biomarker high throughput screening and target translation of breast and gastrointestinal tumor ,Affiliated Zhongshan Hospital of Dalian University ,Dalian ,Liaoning ,China
Pan, Juan;
Affiliation
The Key Laboratory of biomarker high throughput screening and target translation of breast and gastrointestinal tumor ,Affiliated Zhongshan Hospital of Dalian University ,Dalian ,Liaoning ,China
Wang, Piao;
Affiliation
The Key Laboratory of biomarker high throughput screening and target translation of breast and gastrointestinal tumor ,Affiliated Zhongshan Hospital of Dalian University ,Dalian ,Liaoning ,China
Wang, Ruoyu;
Affiliation
The Key Laboratory of biomarker high throughput screening and target translation of breast and gastrointestinal tumor ,Affiliated Zhongshan Hospital of Dalian University ,Dalian ,Liaoning ,China
Liang, Shanshan

As an active constituent in the extract of dried fruits of Schisandra chinensis , Schisandrin B exhibits diverse pharmacological effects, including liver protection, anti-inflammatory and anti-oxidant. Numerous studies have demonstrated that Schisandrin B exhibits significant antitumor activity against various malignant tumors in preclinical studies, which is achieved by inhibiting cell proliferation and metastasis and promoting apoptosis. As a potential antitumor agent, Schisandrin B holds broad application prospects. This review systematically elaborates on the antitumor effect of Schisandrin B and the related molecular mechanism, and preliminarily predicts its antitumor targets by network pharmacology, thereby pave the way for further research, development, and clinical application.

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License Holder: Copyright © 2025 Fang, Pan, Wang, Wang and Liang.

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