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Expression of α(v)β(6)integrin in oral leukoplakia

The distribution of α(v)β(6)integrin was examined in oral leukoplakia, lichen planus and squamous cell carcinomas using immunohistochemistry. Controls included oral mucosal wounds, chronically inflamed and normal oral mucosa. Integrins β(1), β(3), β(4), β(5), fibronectin and tenascin were also studi...

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Detalles Bibliográficos
Autores principales: Hamidi, S, Salo, T, Kainulainen, T, Epstein, J, Lerner, K, Larjava, H
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363375/
https://www.ncbi.nlm.nih.gov/pubmed/10780523
http://dx.doi.org/10.1054/bjoc.1999.1130
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author Hamidi, S
Salo, T
Kainulainen, T
Epstein, J
Lerner, K
Larjava, H
author_facet Hamidi, S
Salo, T
Kainulainen, T
Epstein, J
Lerner, K
Larjava, H
author_sort Hamidi, S
collection PubMed
description The distribution of α(v)β(6)integrin was examined in oral leukoplakia, lichen planus and squamous cell carcinomas using immunohistochemistry. Controls included oral mucosal wounds, chronically inflamed and normal oral mucosa. Integrins β(1), β(3), β(4), β(5), fibronectin and tenascin were also studied. The integrin α(v)β(6)was highly expressed throughout the whole lesion of 90% of the squamous cell carcinomas but was not present in any of the normal specimens. α(v)β(6)integrin was also expressed in 41% of the leukoplakia specimens, and 85% of the lichen planus samples, but in none of the tissues with inflammatory hyperplasia or chronic inflammation. The expression of β1 integrins was localized in the basal layer, and that of the β(4)at the cell surface facing the basement membrane of all specimens. The integrins β(3)and β(5)were absent from all normal and leukoplakia specimens. Fibronectin and tenascin were present in the connective tissue underneath the epithelium of all the sections, and their expression was similar in both α(v)β(6)-positive and α(v)β(6)-negative tissues. A group of 28 leukoplakia patients were followed 1–4 years after first diagnosis. In this group, initially α(v)β(6)integrin-positive leukoplakia specimens had high tendency for disease progression while α(v)β(6)-negative specimens did not progress. These results suggest that the expression of α(v)β(6)integrin could be associated in the malignant transformation of oral leukoplakias. © 2000 Cancer Research Campaign
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spelling pubmed-23633752009-09-10 Expression of α(v)β(6)integrin in oral leukoplakia Hamidi, S Salo, T Kainulainen, T Epstein, J Lerner, K Larjava, H Br J Cancer Regular Article The distribution of α(v)β(6)integrin was examined in oral leukoplakia, lichen planus and squamous cell carcinomas using immunohistochemistry. Controls included oral mucosal wounds, chronically inflamed and normal oral mucosa. Integrins β(1), β(3), β(4), β(5), fibronectin and tenascin were also studied. The integrin α(v)β(6)was highly expressed throughout the whole lesion of 90% of the squamous cell carcinomas but was not present in any of the normal specimens. α(v)β(6)integrin was also expressed in 41% of the leukoplakia specimens, and 85% of the lichen planus samples, but in none of the tissues with inflammatory hyperplasia or chronic inflammation. The expression of β1 integrins was localized in the basal layer, and that of the β(4)at the cell surface facing the basement membrane of all specimens. The integrins β(3)and β(5)were absent from all normal and leukoplakia specimens. Fibronectin and tenascin were present in the connective tissue underneath the epithelium of all the sections, and their expression was similar in both α(v)β(6)-positive and α(v)β(6)-negative tissues. A group of 28 leukoplakia patients were followed 1–4 years after first diagnosis. In this group, initially α(v)β(6)integrin-positive leukoplakia specimens had high tendency for disease progression while α(v)β(6)-negative specimens did not progress. These results suggest that the expression of α(v)β(6)integrin could be associated in the malignant transformation of oral leukoplakias. © 2000 Cancer Research Campaign Nature Publishing Group 2000-04 2000-03-21 /pmc/articles/PMC2363375/ /pubmed/10780523 http://dx.doi.org/10.1054/bjoc.1999.1130 Text en Copyright © 2000 Cancer Research Campaign https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Regular Article
Hamidi, S
Salo, T
Kainulainen, T
Epstein, J
Lerner, K
Larjava, H
Expression of α(v)β(6)integrin in oral leukoplakia
title Expression of α(v)β(6)integrin in oral leukoplakia
title_full Expression of α(v)β(6)integrin in oral leukoplakia
title_fullStr Expression of α(v)β(6)integrin in oral leukoplakia
title_full_unstemmed Expression of α(v)β(6)integrin in oral leukoplakia
title_short Expression of α(v)β(6)integrin in oral leukoplakia
title_sort expression of α(v)β(6)integrin in oral leukoplakia
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363375/
https://www.ncbi.nlm.nih.gov/pubmed/10780523
http://dx.doi.org/10.1054/bjoc.1999.1130
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