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Epidermal growth factor receptor expression in different subtypes of oral lichenoid disease
The oral lichenoid disease (OLD) includes different chronic inflammatory processes such as oral lichen planus (OLP) and oral lichenoid lesions (OLL), both entities with controversial diagnosis and malignant potential. Epidermal growth factor receptor (EFGR) is an important oral carcinogenesis biomar...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medicina Oral S.L.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4192567/ https://www.ncbi.nlm.nih.gov/pubmed/24880441 http://dx.doi.org/10.4317/medoral.19452 |
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author | Cortés-Ramírez, Dionisio A. Rodríguez-Tojo, María J. Coca-Meneses, Juan C. Marichalar-Mendia, Xabier Aguirre-Urizar, José M. |
author_facet | Cortés-Ramírez, Dionisio A. Rodríguez-Tojo, María J. Coca-Meneses, Juan C. Marichalar-Mendia, Xabier Aguirre-Urizar, José M. |
author_sort | Cortés-Ramírez, Dionisio A. |
collection | PubMed |
description | The oral lichenoid disease (OLD) includes different chronic inflammatory processes such as oral lichen planus (OLP) and oral lichenoid lesions (OLL), both entities with controversial diagnosis and malignant potential. Epidermal growth factor receptor (EFGR) is an important oral carcinogenesis biomarker and overexpressed in several oral potentially malignant disorders. Objectives: To analyze the EGFR expression in the OLD to find differences between OLP and OLL, and to correlate it with the main clinical and pathological features. Material and Methods: Forty-four OLD cases were studied and classified according to their clinical (Group C1: only papular lesions / Group C2: papular and other lesions) and histopathological features (Group HT: OLP-typical / Group HC: OLP-compatible) based in previous published criteria. Standard immunohistochemical identification of EGFR protein was performed. Comparative and descriptive statistical analyses were performed. Results: Thirty-five cases (79.5%) showed EGFR overexpression without significant differences between clinical and histopathological groups (p<0.05). Histological groups showed significant differences in the EGFR expression pattern (p=0.016). Conlusions: All OLD samples showed high EGFR expression. The type of clinical lesion was not related with EGFR expression; however, there are differences in the EGFR expression pattern between histological groups that may be related with a different biological profile and malignant risk. Key words:Oral lichenoid disease, oral lichen planus, oral lichenoid lesion, oral carcinogenesis, EGFR. |
format | Online Article Text |
id | pubmed-4192567 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medicina Oral S.L. |
record_format | MEDLINE/PubMed |
spelling | pubmed-41925672014-10-20 Epidermal growth factor receptor expression in different subtypes of oral lichenoid disease Cortés-Ramírez, Dionisio A. Rodríguez-Tojo, María J. Coca-Meneses, Juan C. Marichalar-Mendia, Xabier Aguirre-Urizar, José M. Med Oral Patol Oral Cir Bucal Research The oral lichenoid disease (OLD) includes different chronic inflammatory processes such as oral lichen planus (OLP) and oral lichenoid lesions (OLL), both entities with controversial diagnosis and malignant potential. Epidermal growth factor receptor (EFGR) is an important oral carcinogenesis biomarker and overexpressed in several oral potentially malignant disorders. Objectives: To analyze the EGFR expression in the OLD to find differences between OLP and OLL, and to correlate it with the main clinical and pathological features. Material and Methods: Forty-four OLD cases were studied and classified according to their clinical (Group C1: only papular lesions / Group C2: papular and other lesions) and histopathological features (Group HT: OLP-typical / Group HC: OLP-compatible) based in previous published criteria. Standard immunohistochemical identification of EGFR protein was performed. Comparative and descriptive statistical analyses were performed. Results: Thirty-five cases (79.5%) showed EGFR overexpression without significant differences between clinical and histopathological groups (p<0.05). Histological groups showed significant differences in the EGFR expression pattern (p=0.016). Conlusions: All OLD samples showed high EGFR expression. The type of clinical lesion was not related with EGFR expression; however, there are differences in the EGFR expression pattern between histological groups that may be related with a different biological profile and malignant risk. Key words:Oral lichenoid disease, oral lichen planus, oral lichenoid lesion, oral carcinogenesis, EGFR. Medicina Oral S.L. 2014-09 2014-06-01 /pmc/articles/PMC4192567/ /pubmed/24880441 http://dx.doi.org/10.4317/medoral.19452 Text en Copyright: © 2014 Medicina Oral S.L. http://creativecommons.org/licenses/by/2.5/ 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 work is properly cited. |
spellingShingle | Research Cortés-Ramírez, Dionisio A. Rodríguez-Tojo, María J. Coca-Meneses, Juan C. Marichalar-Mendia, Xabier Aguirre-Urizar, José M. Epidermal growth factor receptor expression in different subtypes of oral lichenoid disease |
title | Epidermal growth factor receptor expression in different
subtypes of oral lichenoid disease |
title_full | Epidermal growth factor receptor expression in different
subtypes of oral lichenoid disease |
title_fullStr | Epidermal growth factor receptor expression in different
subtypes of oral lichenoid disease |
title_full_unstemmed | Epidermal growth factor receptor expression in different
subtypes of oral lichenoid disease |
title_short | Epidermal growth factor receptor expression in different
subtypes of oral lichenoid disease |
title_sort | epidermal growth factor receptor expression in different
subtypes of oral lichenoid disease |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4192567/ https://www.ncbi.nlm.nih.gov/pubmed/24880441 http://dx.doi.org/10.4317/medoral.19452 |
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