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Isoliquiritigenin shows significant anti-ovarian cancer effects with low toxicity as a promising natural candidate for targeted therapy

Isoliquiritigenin shows significant anti-ovarian cancer effects with low toxicity as a promising…
Photo by Julia Koblitz / Unsplash
Key Takeaway
Consider isoliquiritigenin as a promising natural candidate for targeted therapy in ovarian cancer.

This review examines the potential of isoliquiritigenin treatment for ovarian cancer. The scope covers anti-ovarian cancer effects as a primary outcome. The authors synthesize findings indicating significant inhibitory effects against the disease. Specific effect sizes and absolute numbers were not reported in the source text. Safety and tolerability were assessed as low toxicity. Adverse events, serious adverse events, and discontinuations were not reported. Follow-up duration was not reported. The study population and setting were not reported. Funding or conflicts of interest were not reported. The authors note that isoliquiritigenin is a promising natural candidate for targeted therapy, reversal of drug resistance, and combination therapy. Practice relevance is highlighted as a potential natural candidate for these specific therapeutic goals. Causality was not reported. The certainty of the findings was not reported. Limitations acknowledged by the authors were not reported. The review does not describe a specific study population or intervention comparator beyond the general treatment exposure.

Study Details

Study typeSystematic review
EvidenceLevel 1
PublishedJun 2026
View Original Abstract ↓
Ovarian cancer, one of the most common gynecological malignancies, ranks as the fifth leading cause of cancer death in women. To investigate the mechanism by which isoliquiritigenin (ISL) regulates the JAK/STAT signaling pathway in ovarian cancer intervention, this review integrates cellular, animal, and preclinical studies on ISL treatment for ovarian cancer, explores how ISL modulates the JAK/STAT pathway and affects ovarian cancer cell behavior and the tumor immune microenvironment, and summarizes the related mechanisms and research progress. The results show that ISL exerts significant anti-ovarian cancer effects through multitarget regulation of the JAK/STAT pathway. With the advantages of low toxicity and multi-pathway modulation, ISL is a promising natural candidate for targeted therapy, reversal of drug resistance, and combination therapy in ovarian cancer, thus holding great value for basic research and clinical translation.
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