Differential expression of stem cell-like proteins in normal, hyperplastic and dysplastic oral epithelium

Objective: The identification of stem cells (SC) remains challenging. In the human oral mucosal epithelium, these cells are believed to be in the basal layer (stem cell niche), but their exact location is unclear. The aim of this study was to examine the dysplastic oral epithelium for these SC-like...

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Main Authors: Barakat, S.M.M., Siar, C.H.
Format: Article
Language:English
Published: 2015
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Online Access:http://eprints.um.edu.my/13568/1/Differential_expression_of_stem_cell-like_proteins_in_normal%2C_hyperplastic_and_dysplastic_oral_epithelium.pdf
http://eprints.um.edu.my/13568/
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spelling my.um.eprints.135682015-06-16T06:24:25Z http://eprints.um.edu.my/13568/ Differential expression of stem cell-like proteins in normal, hyperplastic and dysplastic oral epithelium Barakat, S.M.M. Siar, C.H. RK Dentistry Objective: The identification of stem cells (SC) remains challenging. In the human oral mucosal epithelium, these cells are believed to be in the basal layer (stem cell niche), but their exact location is unclear. The aim of this study was to examine the dysplastic oral epithelium for these SC-like proteins in order to assess their diagnostic value as biomarkers complementing the histological grading of dysplasia. Material and Methods: Thirty oral epithelial dysplasia (OED), 25 oral lichen planus (OLP), 10 oral hyperkeratosis and 5 normal oral epithelium (OE) were immunohistochemically examined for four SC markers [integrin beta 1, neuron-glial-2 (NG2), notch 1 (N1) and keratin 15 (K15)]. Results: Three of four SC markers were heterogeneously detected in all samples. K15 overexpression in the lower two-thirds of severe OED suggests an expanded SC niche. Integrin beta 1 distribution pattern was not measurably different between OEDs and control. NG2 was almost negative to absent in all samples examined. N1 expression was weak and highly variable in normal and dysplastic epithelium, making it an unreliable epithelial stem cell marker. Conclusions: Present findings suggest that these markers were unable to identify individual epithelial stem cells. Instead, subpopulations of cells, most probably stem cells and transit amplifying cells with stem cell-like properties were identified in the dysplastic oral epithelium. The characteristic expressions of K15 might be of diagnostic value for oral dysplasia and should be investigated further. 2015 Article PeerReviewed application/pdf en http://eprints.um.edu.my/13568/1/Differential_expression_of_stem_cell-like_proteins_in_normal%2C_hyperplastic_and_dysplastic_oral_epithelium.pdf Barakat, S.M.M. and Siar, C.H. (2015) Differential expression of stem cell-like proteins in normal, hyperplastic and dysplastic oral epithelium. Journal of Applied Oral Science. ISSN 1678-7757 10.1590/1678-775720140245
institution Universiti Malaya
building UM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaya
content_source UM Research Repository
url_provider http://eprints.um.edu.my/
language English
topic RK Dentistry
spellingShingle RK Dentistry
Barakat, S.M.M.
Siar, C.H.
Differential expression of stem cell-like proteins in normal, hyperplastic and dysplastic oral epithelium
description Objective: The identification of stem cells (SC) remains challenging. In the human oral mucosal epithelium, these cells are believed to be in the basal layer (stem cell niche), but their exact location is unclear. The aim of this study was to examine the dysplastic oral epithelium for these SC-like proteins in order to assess their diagnostic value as biomarkers complementing the histological grading of dysplasia. Material and Methods: Thirty oral epithelial dysplasia (OED), 25 oral lichen planus (OLP), 10 oral hyperkeratosis and 5 normal oral epithelium (OE) were immunohistochemically examined for four SC markers [integrin beta 1, neuron-glial-2 (NG2), notch 1 (N1) and keratin 15 (K15)]. Results: Three of four SC markers were heterogeneously detected in all samples. K15 overexpression in the lower two-thirds of severe OED suggests an expanded SC niche. Integrin beta 1 distribution pattern was not measurably different between OEDs and control. NG2 was almost negative to absent in all samples examined. N1 expression was weak and highly variable in normal and dysplastic epithelium, making it an unreliable epithelial stem cell marker. Conclusions: Present findings suggest that these markers were unable to identify individual epithelial stem cells. Instead, subpopulations of cells, most probably stem cells and transit amplifying cells with stem cell-like properties were identified in the dysplastic oral epithelium. The characteristic expressions of K15 might be of diagnostic value for oral dysplasia and should be investigated further.
format Article
author Barakat, S.M.M.
Siar, C.H.
author_facet Barakat, S.M.M.
Siar, C.H.
author_sort Barakat, S.M.M.
title Differential expression of stem cell-like proteins in normal, hyperplastic and dysplastic oral epithelium
title_short Differential expression of stem cell-like proteins in normal, hyperplastic and dysplastic oral epithelium
title_full Differential expression of stem cell-like proteins in normal, hyperplastic and dysplastic oral epithelium
title_fullStr Differential expression of stem cell-like proteins in normal, hyperplastic and dysplastic oral epithelium
title_full_unstemmed Differential expression of stem cell-like proteins in normal, hyperplastic and dysplastic oral epithelium
title_sort differential expression of stem cell-like proteins in normal, hyperplastic and dysplastic oral epithelium
publishDate 2015
url http://eprints.um.edu.my/13568/1/Differential_expression_of_stem_cell-like_proteins_in_normal%2C_hyperplastic_and_dysplastic_oral_epithelium.pdf
http://eprints.um.edu.my/13568/
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