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Immunohistochemical Expression of CD(56) and ALDH(1 )in Common Salivary Gland Tumors

INTRODUCTION: Natural killer (NK) cells, of which CD(56) is a specific marker, play an important role in host defense against tumors. Cancer stem cells, of which aldehyde dehydrogenase isoform 1 (ALDH(1)) is an immunohistochemical marker, are a group of tumorigenic cells which are involved in migrat...

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Autores principales: Seifi, Safoura, Seyedmajidi, Maryam, Salehinejad, Jahanshah, Gholinia, Hemmat, Aliakbarpour, Fatemeh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5168570/
https://www.ncbi.nlm.nih.gov/pubmed/28008389
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author Seifi, Safoura
Seyedmajidi, Maryam
Salehinejad, Jahanshah
Gholinia, Hemmat
Aliakbarpour, Fatemeh
author_facet Seifi, Safoura
Seyedmajidi, Maryam
Salehinejad, Jahanshah
Gholinia, Hemmat
Aliakbarpour, Fatemeh
author_sort Seifi, Safoura
collection PubMed
description INTRODUCTION: Natural killer (NK) cells, of which CD(56) is a specific marker, play an important role in host defense against tumors. Cancer stem cells, of which aldehyde dehydrogenase isoform 1 (ALDH(1)) is an immunohistochemical marker, are a group of tumorigenic cells which are involved in migration and tumor recurrences. We aimed to evaluate the expression of ALDH(1) and CD(56) in common salivary gland tumors, as well as their relationship with each other and with a number of clinicopathologic factors. MATERIALS AND METHODS: Forty-five paraffin blocks of salivary gland tumors (pleomorphic adenoma, mucoepidermoid carcinoma and adenoid cystic carcinoma, 15 samples each) were selected. Malignant tumors were classified into two groups: low-grade (including mucoepidermoid carcinoma grade I) and high-grade (including mucoepidermoid carcinoma grade III and adenoid cystic carcinoma). Immunohistochemical staining for ALDH(1 )and CD(56) markers was performed. Data were analyzed using SPSS (20) and the Chi-square test. RESULTS: CD(56 )expression was significantly higher in benign and high-grade malignant tumors (P=0.01). ALDH(1) overexpressed in all three salivary tumors, but not to statistically significant degree (P=0.54). There was no statistically significant correlation between ALDH(1) and CD(56) expression with demographic factors (age, gender, or location of tumor; P>0.05). CONCLUSION: It appears that the number of NK cells and their function change in different types of salivary gland tumors (benign/malignant) and stroma. NK cells are important components of the anti-tumor system; therefore immune dysfunction is associated with tumor progression in tumors of the salivary gland. ALDH(1) overexpression suggests its role in tumorogenesis, but ALDH(1) is not involved in the morphogenesis of salivary gland tumors.
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spelling pubmed-51685702016-12-22 Immunohistochemical Expression of CD(56) and ALDH(1 )in Common Salivary Gland Tumors Seifi, Safoura Seyedmajidi, Maryam Salehinejad, Jahanshah Gholinia, Hemmat Aliakbarpour, Fatemeh Iran J Otorhinolaryngol Original Article INTRODUCTION: Natural killer (NK) cells, of which CD(56) is a specific marker, play an important role in host defense against tumors. Cancer stem cells, of which aldehyde dehydrogenase isoform 1 (ALDH(1)) is an immunohistochemical marker, are a group of tumorigenic cells which are involved in migration and tumor recurrences. We aimed to evaluate the expression of ALDH(1) and CD(56) in common salivary gland tumors, as well as their relationship with each other and with a number of clinicopathologic factors. MATERIALS AND METHODS: Forty-five paraffin blocks of salivary gland tumors (pleomorphic adenoma, mucoepidermoid carcinoma and adenoid cystic carcinoma, 15 samples each) were selected. Malignant tumors were classified into two groups: low-grade (including mucoepidermoid carcinoma grade I) and high-grade (including mucoepidermoid carcinoma grade III and adenoid cystic carcinoma). Immunohistochemical staining for ALDH(1 )and CD(56) markers was performed. Data were analyzed using SPSS (20) and the Chi-square test. RESULTS: CD(56 )expression was significantly higher in benign and high-grade malignant tumors (P=0.01). ALDH(1) overexpressed in all three salivary tumors, but not to statistically significant degree (P=0.54). There was no statistically significant correlation between ALDH(1) and CD(56) expression with demographic factors (age, gender, or location of tumor; P>0.05). CONCLUSION: It appears that the number of NK cells and their function change in different types of salivary gland tumors (benign/malignant) and stroma. NK cells are important components of the anti-tumor system; therefore immune dysfunction is associated with tumor progression in tumors of the salivary gland. ALDH(1) overexpression suggests its role in tumorogenesis, but ALDH(1) is not involved in the morphogenesis of salivary gland tumors. Mashhad University of Medical Sciences 2016-11 /pmc/articles/PMC5168570/ /pubmed/28008389 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Seifi, Safoura
Seyedmajidi, Maryam
Salehinejad, Jahanshah
Gholinia, Hemmat
Aliakbarpour, Fatemeh
Immunohistochemical Expression of CD(56) and ALDH(1 )in Common Salivary Gland Tumors
title Immunohistochemical Expression of CD(56) and ALDH(1 )in Common Salivary Gland Tumors
title_full Immunohistochemical Expression of CD(56) and ALDH(1 )in Common Salivary Gland Tumors
title_fullStr Immunohistochemical Expression of CD(56) and ALDH(1 )in Common Salivary Gland Tumors
title_full_unstemmed Immunohistochemical Expression of CD(56) and ALDH(1 )in Common Salivary Gland Tumors
title_short Immunohistochemical Expression of CD(56) and ALDH(1 )in Common Salivary Gland Tumors
title_sort immunohistochemical expression of cd(56) and aldh(1 )in common salivary gland tumors
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5168570/
https://www.ncbi.nlm.nih.gov/pubmed/28008389
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