Please use this identifier to cite or link to this item:
https://doi.org/10.1371/journal.pone.0156949
DC Field | Value | |
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dc.title | Differential expression patterns of egf, egfr, and erbb4 in nasal polyp epithelium | |
dc.contributor.author | Duan C. | |
dc.contributor.author | Li C.W. | |
dc.contributor.author | Zhao L. | |
dc.contributor.author | Subramaniam S. | |
dc.contributor.author | Yu X.M. | |
dc.contributor.author | Li Y.Y. | |
dc.contributor.author | De Chen H. | |
dc.contributor.author | Li T.Y. | |
dc.contributor.author | Shen L. | |
dc.contributor.author | Shi L. | |
dc.contributor.author | De Wang Y. | |
dc.date.accessioned | 2020-03-19T07:48:09Z | |
dc.date.available | 2020-03-19T07:48:09Z | |
dc.date.issued | 2016 | |
dc.identifier.citation | Duan C., Li C.W., Zhao L., Subramaniam S., Yu X.M., Li Y.Y., De Chen H., Li T.Y., Shen L., Shi L., De Wang Y. (2016). Differential expression patterns of egf, egfr, and erbb4 in nasal polyp epithelium. PLoS ONE 11 (6) : e0156949. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0156949 | |
dc.identifier.issn | 19326203 | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/165746 | |
dc.description.abstract | Epidermal growth factor receptors play an important role in airway epithelial cell growth and differentiation. The current study investigates the expression profiles of EGF, EGFR and ERBB4 in patients with nasal polyps (NP), and their response to glucocorticosteroid (GC) treatment. Fifty patients with NP (40 without GC treatment and 10 with oral GC) and 20 control subjects with septal deviation were recruited into the study. Protein levels of EGF, EGFR, and ERBB4 were evaluated by immune-staining. In healthy nasal epithelium, EGF and EGFR localized within p63 + basal cells, while ERBB4 localized within ciliated cells. GCnaïve NP epithelium showed weak expression of EGF in 90% of samples versus 5% of controls. EGFR was significantly increased in the epithelium with basal cell hyperplasia from GC-naïve NPs (78%, 31/40) compared to controls (23%, 4/17). EGFR was also found in some degranulating goblet cells. ERBB4 expression was significantly higher in hyperplastic epithelium from GC-naïve NPs (65%, 26/40) than in controls (6%, 1/17). GC treatment restored the EGF expression and normalized the EGFR and ERBB4 expression in NPs. Differential expression patterns of EGF, EGFR, and ERBB4 are essential in epithelial restitution and remodeling in nasal epithelium. © 2016 Duan et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. | |
dc.publisher | Public Library of Science | |
dc.source | Unpaywall 20200320 | |
dc.subject | alpha tubulin | |
dc.subject | epidermal growth factor | |
dc.subject | epidermal growth factor receptor | |
dc.subject | epidermal growth factor receptor 4 | |
dc.subject | glucocorticoid | |
dc.subject | messenger RNA | |
dc.subject | protein p63 | |
dc.subject | EGFR protein, human | |
dc.subject | epidermal growth factor | |
dc.subject | epidermal growth factor receptor | |
dc.subject | epidermal growth factor receptor 4 | |
dc.subject | ERBB4 protein, human | |
dc.subject | adult | |
dc.subject | Article | |
dc.subject | basal cell | |
dc.subject | cell hyperplasia | |
dc.subject | cell infiltration | |
dc.subject | cell surface | |
dc.subject | cellular distribution | |
dc.subject | Chinese | |
dc.subject | comparative study | |
dc.subject | controlled study | |
dc.subject | disease association | |
dc.subject | female | |
dc.subject | gene expression profiling | |
dc.subject | gene expression regulation | |
dc.subject | goblet cell | |
dc.subject | histopathology | |
dc.subject | human | |
dc.subject | human cell | |
dc.subject | human tissue | |
dc.subject | inflammatory cell | |
dc.subject | intracellular signaling | |
dc.subject | major clinical study | |
dc.subject | male | |
dc.subject | molecular dynamics | |
dc.subject | nose mucosa | |
dc.subject | nose polyp | |
dc.subject | polypectomy | |
dc.subject | protein expression | |
dc.subject | protein localization | |
dc.subject | transcription regulation | |
dc.subject | upregulation | |
dc.subject | case control study | |
dc.subject | gene expression profiling | |
dc.subject | genetics | |
dc.subject | metabolism | |
dc.subject | middle aged | |
dc.subject | nose mucosa | |
dc.subject | nose polyp | |
dc.subject | pathology | |
dc.subject | physiology | |
dc.subject | regeneration | |
dc.subject | young adult | |
dc.subject | Adult | |
dc.subject | Case-Control Studies | |
dc.subject | Epidermal Growth Factor | |
dc.subject | Female | |
dc.subject | Gene Expression Profiling | |
dc.subject | Humans | |
dc.subject | Male | |
dc.subject | Middle Aged | |
dc.subject | Nasal Mucosa | |
dc.subject | Nasal Polyps | |
dc.subject | Receptor, Epidermal Growth Factor | |
dc.subject | Receptor, ErbB-4 | |
dc.subject | Regeneration | |
dc.subject | Young Adult | |
dc.type | Article | |
dc.contributor.department | OTOLARYNGOLOGY | |
dc.contributor.department | SAW SWEE HOCK SCHOOL OF PUBLIC HEALTH | |
dc.contributor.department | DEAN'S OFFICE (MEDICINE) | |
dc.description.doi | 10.1371/journal.pone.0156949 | |
dc.description.sourcetitle | PLoS ONE | |
dc.description.volume | 11 | |
dc.description.issue | 6 | |
dc.description.page | e0156949 | |
Appears in Collections: | Elements Staff Publications |
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