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Potential Role of S100A8 in Cutaneous Squamous Cell Carcinoma Differentiation
BACKGROUND: S100A8 is differentially expressed in various cell types and is associated with a number of malignant disorders. S100A8 may affect tumor biology. However, its role in cutaneous squamous cell carcinoma (SCC) is not well established. OBJECTIVE: This study aims to investigate the relationsh...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Dermatological Association; The Korean Society for Investigative Dermatology
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4828380/ https://www.ncbi.nlm.nih.gov/pubmed/27081264 http://dx.doi.org/10.5021/ad.2016.28.2.179 |
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author | Shin, Jung-Min Chang, In-Kyu Lee, Young-Ho Yeo, Min-Kyung Kim, Jin-Man Sohn, Kyung-Cheol Im, Myung Seo, Young-Joon Kim, Chang-Deok Lee, Jeung-Hoon Lee, Young |
author_facet | Shin, Jung-Min Chang, In-Kyu Lee, Young-Ho Yeo, Min-Kyung Kim, Jin-Man Sohn, Kyung-Cheol Im, Myung Seo, Young-Joon Kim, Chang-Deok Lee, Jeung-Hoon Lee, Young |
author_sort | Shin, Jung-Min |
collection | PubMed |
description | BACKGROUND: S100A8 is differentially expressed in various cell types and is associated with a number of malignant disorders. S100A8 may affect tumor biology. However, its role in cutaneous squamous cell carcinoma (SCC) is not well established. OBJECTIVE: This study aims to investigate the relationship between S100A8 and cutaneous SCC development. METHODS: We performed immunohistochemical staining to detect S100A8 expression in facial skin specimens of premalignant actinic keratosis (AK), malignant SCC, and normal tissues. In addition, we utilized postconfluence and high calcium-induced differentiation in a culture system model. Furthermore, we constructed a recombinant adenovirus expressing GFP-tagged S100A8 to investigate the role of S100A8 in SCC cell differentiation. RESULTS: S100A8 was significantly overexpressed in human cutaneous SCC compared to that in normal and AK tissues. S100A8 was gradually upregulated in SCC cells in a post-confluence-induced differentiation model. Overexpression of S100A8 in SCC cells induced by adenoviral transduction led to increased expression levels of differentiation markers, such as loricrin, involucrin, and filaggrin. S100A8 overexpression also increased loricrin and involucrin luciferase activity. CONCLUSION: S100A8 regulates cutaneous SCC differentiation and induces well-differentiated SCC formation in skin. |
format | Online Article Text |
id | pubmed-4828380 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Korean Dermatological Association; The Korean Society for Investigative Dermatology |
record_format | MEDLINE/PubMed |
spelling | pubmed-48283802016-04-14 Potential Role of S100A8 in Cutaneous Squamous Cell Carcinoma Differentiation Shin, Jung-Min Chang, In-Kyu Lee, Young-Ho Yeo, Min-Kyung Kim, Jin-Man Sohn, Kyung-Cheol Im, Myung Seo, Young-Joon Kim, Chang-Deok Lee, Jeung-Hoon Lee, Young Ann Dermatol Original Article BACKGROUND: S100A8 is differentially expressed in various cell types and is associated with a number of malignant disorders. S100A8 may affect tumor biology. However, its role in cutaneous squamous cell carcinoma (SCC) is not well established. OBJECTIVE: This study aims to investigate the relationship between S100A8 and cutaneous SCC development. METHODS: We performed immunohistochemical staining to detect S100A8 expression in facial skin specimens of premalignant actinic keratosis (AK), malignant SCC, and normal tissues. In addition, we utilized postconfluence and high calcium-induced differentiation in a culture system model. Furthermore, we constructed a recombinant adenovirus expressing GFP-tagged S100A8 to investigate the role of S100A8 in SCC cell differentiation. RESULTS: S100A8 was significantly overexpressed in human cutaneous SCC compared to that in normal and AK tissues. S100A8 was gradually upregulated in SCC cells in a post-confluence-induced differentiation model. Overexpression of S100A8 in SCC cells induced by adenoviral transduction led to increased expression levels of differentiation markers, such as loricrin, involucrin, and filaggrin. S100A8 overexpression also increased loricrin and involucrin luciferase activity. CONCLUSION: S100A8 regulates cutaneous SCC differentiation and induces well-differentiated SCC formation in skin. Korean Dermatological Association; The Korean Society for Investigative Dermatology 2016-04 2016-03-31 /pmc/articles/PMC4828380/ /pubmed/27081264 http://dx.doi.org/10.5021/ad.2016.28.2.179 Text en Copyright © 2016 The Korean Dermatological Association and The Korean Society for Investigative Dermatology http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Shin, Jung-Min Chang, In-Kyu Lee, Young-Ho Yeo, Min-Kyung Kim, Jin-Man Sohn, Kyung-Cheol Im, Myung Seo, Young-Joon Kim, Chang-Deok Lee, Jeung-Hoon Lee, Young Potential Role of S100A8 in Cutaneous Squamous Cell Carcinoma Differentiation |
title | Potential Role of S100A8 in Cutaneous Squamous Cell Carcinoma Differentiation |
title_full | Potential Role of S100A8 in Cutaneous Squamous Cell Carcinoma Differentiation |
title_fullStr | Potential Role of S100A8 in Cutaneous Squamous Cell Carcinoma Differentiation |
title_full_unstemmed | Potential Role of S100A8 in Cutaneous Squamous Cell Carcinoma Differentiation |
title_short | Potential Role of S100A8 in Cutaneous Squamous Cell Carcinoma Differentiation |
title_sort | potential role of s100a8 in cutaneous squamous cell carcinoma differentiation |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4828380/ https://www.ncbi.nlm.nih.gov/pubmed/27081264 http://dx.doi.org/10.5021/ad.2016.28.2.179 |
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