ArticleCell biochemistry and biophysics2026
Investigating the Therapeutic Potential of Agarwood Nanoemulsion in Modulating TGF-β-Induced Airway Remodelling in BEAS-2B Cells.
Article in Cell biochemistry and biophysics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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Who cites it
2 citing papers in PubMed.
- Lipid Modifications and Inflammation in Cardiometabolic and Vascular Disease: Perspectives from a Special Edition Honoring a Pioneer Scientist.Cell biochemistry and biophysics · 2026Article
- Natural medicines for asthma management: mechanisms aligned with endotypes and multi-dimensional intervention.Frontiers in pharmacology · 2026Review
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Authors and funding
7 authors.
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Abstract
Chronic respiratory diseases such as asthma, chronic obstructive pulmonary disease (COPD), and pulmonary fibrosis are significant global health concerns, characterised by inflammation, oxidative stress, and airway remodelling. These processes are driven by multiple cytokines, with transforming growth factor-beta (TGF-β) playing a central role in the remodelling process. TGF-β triggers pathways that promote epithelial-mesenchymal transition (EMT), excessive extracellular matrix deposition, and increased oxidative stress, all of which contribute to airway remodelling. Despite availability of therapies including corticosteroids and bronchodilators that offer symptomatic relief, these fail to address the underlying causes of oxidative damage, persistent inflammation, and fibrosis, limiting long-term effectiveness. This study investigates the effects of Agarwood Nanoemulsion (AW-NE) on TGF-β-induced oxidative stress, inflammation, and airway remodelling in BEAS-2B cells, in vitro. The results show that AW-NE significantly reduces oxidative stress and restores nitric oxide (NO) production, suppressed by TGF-β activation. AW-NE also inhibits TGF-β-induced cell migration, indicating potential in modulating TGF-β-induced airway remodelling. Additionally, AW-NE treatment decreased the expression of key inflammatory and pro-remodelling proteins, including MMP-9, angiogenin, and pentraxin-3 (PTX-3). These findings suggest that, while current treatments primarily manage symptoms, AW-NE shows potential in addressing the underlying pathophysiology. Further in vivo studies are required to confirm its therapeutic efficacy.
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