# Effect of formononetin on progressive pulmonary pathologies: multitarget mechanisms and therapeutic prospects

**Authors:** Dan Yan, Saibin Wang

PMC · DOI: 10.3389/fphar.2025.1645964 · 2025-10-22

## TL;DR

Formononetin, a natural compound, shows promise for treating various lung diseases by targeting multiple biological pathways, though its use is limited by poor solubility and bioavailability.

## Contribution

This review highlights formononetin's multitarget mechanisms and novel delivery systems to enhance its therapeutic potential for respiratory diseases.

## Key findings

- Formononetin reduces oxidative stress, inflammation, and fibrosis in lung diseases through Nrf2/HO-1 activation and NF-κB inhibition.
- Novel delivery systems like FMN@BSA nanoparticles improve formononetin's stability and bioavailability.
- Preclinical studies show formononetin attenuates lung injury and slows fibrosis progression.

## Abstract

Formononetin (FMN), an isoflavone derived from Radix Astragali and red clover, has promising therapeutic potential for a wide spectrum of respiratory diseases, including acute lung injury (ALI), pulmonary arterial hypertension (PAH), chronic obstructive pulmonary disease (COPD), asthma, and pulmonary fibrosis (PF). Mechanistically, FMN alleviates oxidative stress, inflammation, and fibrotic remodelling by activating Nrf2/HO-1, inhibiting NF-κB, and modulating the activity of the TGF-β/Smad signalling pathway. Evidence from cellular and animal studies has shown that FMN attenuates lung injury, prevents vascular remodelling, and slows the progression of fibrosis. However, its clinical translation is hampered by poor solubility, rapid metabolism, and low oral bioavailability, which limit its therapeutic effectiveness. To overcome these challenges, novel delivery systems—such as albumin-based FMN nanoparticles (FMN@BSA nanoparticles)—have been developed to increase the stability, bioavailability, and pharmacological potency of FMN. Despite encouraging preclinical outcomes, further studies are needed to clarify upstream mechanisms and conduct rigorous clinical evaluations. This review highlights the potential of FMN as a novel therapeutic candidate for respiratory diseases by summarizing its mechanisms of action and underscoring the importance of advanced delivery strategies in facilitating its future clinical application.

## Linked entities

- **Genes:** GABPA (GA binding protein transcription factor subunit alpha) [NCBI Gene 2551], HMOX1 (heme oxygenase 1) [NCBI Gene 3162], NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790], TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040], Smox (Smad on X) [NCBI Gene 31738]
- **Chemicals:** formononetin (PubChem CID 5280378)
- **Diseases:** acute lung injury (MONDO:0006502), pulmonary arterial hypertension (MONDO:0015924), chronic obstructive pulmonary disease (MONDO:0005002), asthma (MONDO:0004979), pulmonary fibrosis (MONDO:0002771)

## Full-text entities

- **Genes:** HMOX1 (heme oxygenase 1) [NCBI Gene 3162] {aka HMOX1D, HO-1, HSP32, bK286B10}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, NFE2L2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 4780] {aka IMDDHH, NRF2, Nrf-2}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}
- **Diseases:** PF (MESH:D011658), inflammation (MESH:D007249), lung injury (MESH:D055370), PAH (MESH:D000081029), pulmonary pathologies (MESH:D008171), vascular remodelling (MESH:D066253), fibrosis (MESH:D005355), asthma (MESH:D001249), respiratory diseases (MESH:D012140), COPD (MESH:D029424), ALI (MESH:D055371)
- **Chemicals:** FMN (MESH:C007768), Astragali (-), isoflavone (MESH:D007529)
- **Species:** Trifolium pratense (peavine clover, species) [taxon 57577]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12585962/full.md

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Source: https://tomesphere.com/paper/PMC12585962