# Cangfu Daotan decoction treats PCOS-IR through the IL6/JAK2/STAT3/FOXO4 signaling pathway

**Authors:** Wenhan Ju, Qianwen Zhang, Yue Wang, Keying Pan, Yuan Li, Shuai Zhao, Fang Lian

PMC · DOI: 10.3389/fendo.2025.1661000 · Frontiers in Endocrinology · 2026-01-07

## TL;DR

This study shows that Cangfu Daotan Decoction improves PCOS with insulin resistance by targeting a specific signaling pathway.

## Contribution

The study identifies the IL6/JAK2/STAT3/FOXO4 pathway as a novel target for Cangfu Daotan Decoction in treating PCOS-IR.

## Key findings

- Cangfu Daotan Decoction improved ovarian function and reduced insulin resistance in PCOS-IR mice.
- The decoction enhanced glucose intake in granulosa cells under PCOS-IR conditions.
- CDD suppressed the IL6/JAK2/STAT3/FOXO4 signaling pathway in both in vivo and in vitro models.

## Abstract

This study aimed to investigate the protective effects and underlying mechanisms of Cangfu Daotan Decoction (CDD) in both vivo and in vitro models of polycystic ovary syndrome with insulin resistance (PCOS-IR).

Active compounds in CDD were identified using UPLC-HRMS. Network pharmacology and molecular docking analyses were employed to predict key molecular targets. A nd a high-fat diet. In vitro, KGN cells were used to simulate granulosa cell dysfunction associated with PCOS-IR. The regulatory effects of CDD on the IL6/JAK2/STAT3/FOXO4 signaling pathway were further evaluated.

Fifteen active compounds in CDD were preliminarily identified. Ninety-four potential target genes related to the treatment of PCOS-IR were screened. Network pharmacology and molecular docking analyses indicated strong binding affinities between STAT3 and several active compounds of CDD. CDD improved ovarian function and reduced insulin resistance in PCOS model mice. In vitro, CDD also enhanced glucose intake in granulosa cells under PCOS-IR conditions. Both in vivo and in vitro experiments demonstrated that CDD significantly suppressed activation of the IL6/JAK2/STAT3/FOXO4 signaling pathway.

CDD may improve ovarian function and insulin resistance in PCOS-IR mice by modulating the IL6/JAK2/STAT3/FOXO4 signaling pathway.

## Linked entities

- **Genes:** IL6 (interleukin 6) [NCBI Gene 3569], JAK2 (Janus kinase 2) [NCBI Gene 3717], STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774], FOXO4 (forkhead box O4) [NCBI Gene 4303]
- **Diseases:** polycystic ovary syndrome (MONDO:0008487)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Foxo4 (forkhead box O4) [NCBI Gene 54601] {aka Afxh, Mllt7, afx}, Jak2 (Janus kinase 2) [NCBI Gene 16452] {aka Fd17}, Stat3 (signal transducer and activator of transcription 3) [NCBI Gene 20848] {aka 1110034C02Rik, Aprf}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}
- **Diseases:** insulin resistance (MESH:D007333), IR (MESH:C537629), PCOS (MESH:D011085)
- **Chemicals:** glucose (MESH:D005947), Cangfu Daotan (-)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12819200/full.md

## References

65 references — full list in the complete paper: https://tomesphere.com/paper/PMC12819200/full.md

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Source: https://tomesphere.com/paper/PMC12819200