Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/98672
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dc.contributorDepartment of Civil and Environmental Engineeringen_US
dc.creatorDonovan, Cen_US
dc.creatorBai, Xen_US
dc.creatorChan, YLen_US
dc.creatorFeng, Men_US
dc.creatorHo, KFen_US
dc.creatorGuo, Hen_US
dc.creatorChen, Hen_US
dc.creatorOliver, BGen_US
dc.date.accessioned2023-05-10T02:03:55Z-
dc.date.available2023-05-10T02:03:55Z-
dc.identifier.urihttp://hdl.handle.net/10397/98672-
dc.language.isoenen_US
dc.publisherMDPI AGen_US
dc.rights© 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).en_US
dc.rightsThe following publication Donovan, C., Bai, X., Chan, Y. L., Feng, M., Ho, K. F., Guo, H., ... & Oliver, B. G. (2023). Tenascin C in Lung Diseases. Biology, 12(2), 199 is available at https://doi.org/10.3390/biology12020199.en_US
dc.subjectAsthmaen_US
dc.subjectCOPDen_US
dc.subjectFoetal programmingen_US
dc.subjectLung canceren_US
dc.subjectLung developmenten_US
dc.subjectParticular matteren_US
dc.titleTenascin C in lung diseasesen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume12en_US
dc.identifier.issue2en_US
dc.identifier.doi10.3390/biology12020199en_US
dcterms.abstractTenascin C (TNC) is a multifunctional large extracellular matrix protein involved in numerous cellular processes in embryonic development and can be increased in disease, or under conditions of trauma or cell stress in adults. However, the role of TNC in lung diseases remains unclear. In this study, we investigated the expression of TNC during development, in offspring following maternal particulate matter (PM) exposure, asthma, chronic obstructive pulmonary disease (COPD) and lung cancer. TNC expression is increased during lung development in biopsy cells, endothelial cells, mesenchymal cells, and epithelial cells. Maternal PM exposure increased TNC and collagen deposition, which was not affected by the removal of PM exposure after pregnancy. TNC expression was also increased in basal epithelial cells and fibroblasts in patients with asthma and AT2 and endothelial cells in patients with COPD. Furthermore, there was an increase in the expression of TNC in stage II compared to stage IA lung cancer; however, overall survival analysis showed no correlation between levels of TNC and survival. In conclusion, TNC is increased during lung development, in offspring following maternal PM exposure, and in asthma, COPD, and lung cancer tissues. Therefore, targeting TNC may provide a novel therapeutic target for lung diseases.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationBiology, Feb. 2023, v. 12, no. 2, 199en_US
dcterms.isPartOfBiologyen_US
dcterms.issued2023-02-
dc.identifier.isiWOS:000938930900001-
dc.identifier.scopus2-s2.0-85148949401-
dc.identifier.eissn2079-7737en_US
dc.identifier.artn199en_US
dc.description.validate202305 bcvcen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOS-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNational Health & Medical Research Council; NHMRC Australia; Hong Kong Polytechnic Universityen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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