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Investigating the Therapeutic Potential of Agarwood Nanoemulsion in Modulating TGF-β-Induced Airway Remodelling in BEAS-2B Cells
Univ Technol Sydney, Grad Sch Hlth, Discipline Pharm, Ultimo, NSW 2007, Australia.;DeAurora Pty Ltd, Dean, Vic 3363, Australia..
Univ Technol Sydney, Grad Sch Hlth, Discipline Pharm, Ultimo, NSW 2007, Australia..
DeAurora Pty Ltd, Dean, Vic 3363, Australia..
Centenary Inst, Ctr Inflammat, Sydney 2007, Australia.;Univ Technol Sydney, Fac Sci, Sch Life Sci, Sydney 2007, Australia.;Macquarie Univ, Woolcock Inst Med Res, Sydney, NSW 2113, Australia.;Western Sydney Univ, NICM Hlth Res Inst, Westmead, NSW 2145, Australia..ORCID iD: 0000-0002-3591-2080
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2026 (English)In: Cell Biochemistry and Biophysics, ISSN 1085-9195, E-ISSN 1559-0283, Vol. 84, no 1, p. 1047-1056Article in journal (Refereed) Published
Abstract [en]

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-beta) playing a central role in the remodelling process. TGF-beta 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-beta-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-beta activation. AW-NE also inhibits TGF-beta-induced cell migration, indicating potential in modulating TGF-beta-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.

Place, publisher, year, edition, pages
Springer Nature, 2026. Vol. 84, no 1, p. 1047-1056
Keywords [en]
Chronic respiratory diseases, Agarwood oil, Nanoemulsion, Inflammation, Oxidative stress, Airway remodelling
National Category
Respiratory Medicine and Allergy Cell and Molecular Biology
Identifiers
URN: urn:nbn:se:uu:diva-593978OAI: oai:DiVA.org:uu-593978DiVA, id: diva2:2085355
Available from: 2026-07-08 Created: 2026-07-08 Last updated: 2026-07-08

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