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Association of cytokeratin 17 expression with differentiation in oral squamous cell carcinoma

PURPOSE: The aim of this study was to confirm the expression profile of cytokeratin (CK)17 in comparison with that of CK13 in oral squamous cell carcinoma (OSCC) and leukoplakia and to clarify an association of CK17 with the OSCC differentiation. MATERIALS: The expression of CK17 and CK13 was immuno...

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Autores principales: Kitamura, Ryoji, Toyoshima, Takeshi, Tanaka, Hideaki, Kawano, Shintaro, Kiyosue, Takahiro, Matsubara, Ryota, Goto, Yuichi, Hirano, Mitsuhiro, Oobu, Kazunari, Nakamura, Seiji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2012
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3397222/
https://www.ncbi.nlm.nih.gov/pubmed/22466643
http://dx.doi.org/10.1007/s00432-012-1202-6
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author Kitamura, Ryoji
Toyoshima, Takeshi
Tanaka, Hideaki
Kawano, Shintaro
Kiyosue, Takahiro
Matsubara, Ryota
Goto, Yuichi
Hirano, Mitsuhiro
Oobu, Kazunari
Nakamura, Seiji
author_facet Kitamura, Ryoji
Toyoshima, Takeshi
Tanaka, Hideaki
Kawano, Shintaro
Kiyosue, Takahiro
Matsubara, Ryota
Goto, Yuichi
Hirano, Mitsuhiro
Oobu, Kazunari
Nakamura, Seiji
author_sort Kitamura, Ryoji
collection PubMed
description PURPOSE: The aim of this study was to confirm the expression profile of cytokeratin (CK)17 in comparison with that of CK13 in oral squamous cell carcinoma (OSCC) and leukoplakia and to clarify an association of CK17 with the OSCC differentiation. MATERIALS: The expression of CK17 and CK13 was immunohistochemically examined in 105 patients with OSCC and 108 patients with leukoplakia. A correlation of CK expression with clinicopathological variables was carried out. The over-expression levels of CK17 mRNA were analyzed by real-time RT-PCR in 5 OSCC cell lines (HSC-2, HSC-3, SAS, SQUU-A, SQUU-B). RESULTS: CK17 and CK13 were detected in 101 (96.2 %) and three (2.9 %) of the 105 OSCCs, respectively. CK17 was significantly expressed in well-differentiated OSCC compared to moderately/poorly differentiated OSCC (p < 0.01). As detected in 19 of the 34 dysplastic leukoplakias (55.9 %) and 36 of the 74 hyperplastic leukoplakias (48.6 %), CK17 was significantly expressed in dysplastic leukoplakias (p < 0.01). As detected in 11 of the 34 dysplastic (32.4 %) and 52 of the 74 hyperplastic leukoplakias (70.3 %), CK13 was significantly expressed in hyperplastic leukoplakias (p < 0.01). The relative expression of CK17 mRNA in HSC-2 was significantly higher than in HSC-3 and SAS (p < 0.05). Moreover, the relative expression of CK17 mRNA in SQUU-A was significantly higher than in SQUU-B (p < 0.05). CONCLUSION: CK17 expression could be associated with the differentiation and the malignancy of OSCC. A combination pattern of CK17/CK13 might be a suitable marker of malignant transformation.
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spelling pubmed-33972222012-07-23 Association of cytokeratin 17 expression with differentiation in oral squamous cell carcinoma Kitamura, Ryoji Toyoshima, Takeshi Tanaka, Hideaki Kawano, Shintaro Kiyosue, Takahiro Matsubara, Ryota Goto, Yuichi Hirano, Mitsuhiro Oobu, Kazunari Nakamura, Seiji J Cancer Res Clin Oncol Original Paper PURPOSE: The aim of this study was to confirm the expression profile of cytokeratin (CK)17 in comparison with that of CK13 in oral squamous cell carcinoma (OSCC) and leukoplakia and to clarify an association of CK17 with the OSCC differentiation. MATERIALS: The expression of CK17 and CK13 was immunohistochemically examined in 105 patients with OSCC and 108 patients with leukoplakia. A correlation of CK expression with clinicopathological variables was carried out. The over-expression levels of CK17 mRNA were analyzed by real-time RT-PCR in 5 OSCC cell lines (HSC-2, HSC-3, SAS, SQUU-A, SQUU-B). RESULTS: CK17 and CK13 were detected in 101 (96.2 %) and three (2.9 %) of the 105 OSCCs, respectively. CK17 was significantly expressed in well-differentiated OSCC compared to moderately/poorly differentiated OSCC (p < 0.01). As detected in 19 of the 34 dysplastic leukoplakias (55.9 %) and 36 of the 74 hyperplastic leukoplakias (48.6 %), CK17 was significantly expressed in dysplastic leukoplakias (p < 0.01). As detected in 11 of the 34 dysplastic (32.4 %) and 52 of the 74 hyperplastic leukoplakias (70.3 %), CK13 was significantly expressed in hyperplastic leukoplakias (p < 0.01). The relative expression of CK17 mRNA in HSC-2 was significantly higher than in HSC-3 and SAS (p < 0.05). Moreover, the relative expression of CK17 mRNA in SQUU-A was significantly higher than in SQUU-B (p < 0.05). CONCLUSION: CK17 expression could be associated with the differentiation and the malignancy of OSCC. A combination pattern of CK17/CK13 might be a suitable marker of malignant transformation. Springer-Verlag 2012-04-03 2012 /pmc/articles/PMC3397222/ /pubmed/22466643 http://dx.doi.org/10.1007/s00432-012-1202-6 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Paper
Kitamura, Ryoji
Toyoshima, Takeshi
Tanaka, Hideaki
Kawano, Shintaro
Kiyosue, Takahiro
Matsubara, Ryota
Goto, Yuichi
Hirano, Mitsuhiro
Oobu, Kazunari
Nakamura, Seiji
Association of cytokeratin 17 expression with differentiation in oral squamous cell carcinoma
title Association of cytokeratin 17 expression with differentiation in oral squamous cell carcinoma
title_full Association of cytokeratin 17 expression with differentiation in oral squamous cell carcinoma
title_fullStr Association of cytokeratin 17 expression with differentiation in oral squamous cell carcinoma
title_full_unstemmed Association of cytokeratin 17 expression with differentiation in oral squamous cell carcinoma
title_short Association of cytokeratin 17 expression with differentiation in oral squamous cell carcinoma
title_sort association of cytokeratin 17 expression with differentiation in oral squamous cell carcinoma
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3397222/
https://www.ncbi.nlm.nih.gov/pubmed/22466643
http://dx.doi.org/10.1007/s00432-012-1202-6
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