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The study of CD117 expression in glial tumors and its relationship with the tumor-type and grade

BACKGROUND: CD117 is a thyrosin kinase receptor encoded by c-kit proto-oncogene. It is expressed during normal development in some tissues and also in a subset of neoplasia especially gastrointestinal stromal tumors (GISTs). Treatment with thyrosin kinase inhibitors (e.g., Imatinib) is useful in CD1...

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Autores principales: Mahzouni, Parvin, Jafari, Mohsen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3525034/
https://www.ncbi.nlm.nih.gov/pubmed/23264790
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author Mahzouni, Parvin
Jafari, Mohsen
author_facet Mahzouni, Parvin
Jafari, Mohsen
author_sort Mahzouni, Parvin
collection PubMed
description BACKGROUND: CD117 is a thyrosin kinase receptor encoded by c-kit proto-oncogene. It is expressed during normal development in some tissues and also in a subset of neoplasia especially gastrointestinal stromal tumors (GISTs). Treatment with thyrosin kinase inhibitors (e.g., Imatinib) is useful in CD117- positive GISTs. The goal of this study is to investigate the expression of CD117 in glial tumors as a potential diagnostic marker and target for therapy. MATERIALS AND METHODS: in this descriptive-analytical study, paraffin- embedded tissue blocks from 50 cases of glial tumors (various histological types and grades) were selected in a convenience sampling for the CD117 immunhistochemical study including expression of the marker, staining intensity, and percentage of the stained cells. The results were analyzed by Chi-square and Mann–Whitney tests. RESULTS: CD117 expression was detected in about 76% of glial tumors but the frequency of the expression showed no statistically significant relationship with the tumor type (P = 0.829). Although CD117 immunoreactivity was more frequent in high-grade tumors (84%) compared to the low-grade ones (68%), no statistically significant relationship was found between the CD117 expression and grade of the tumor (P = 0.09). Staining intensity and percentage of stained cells in high-grade tumors were significantly more than in low-grade tumors (P values of 0.046 and 0.023, respectively). CONCLUSION: according to the statistically significant difference in the staining intensity and percentage of the stained cells between the low-grade and high-grade glial tumors, these two parameters may be useful for making distinction between various grades of these tumors. Moreover, according to the prominent expression of CD117 in high-grade gliomas, these tumors may be potential candidates for treatment with thyrosin kinase inhibitors.
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spelling pubmed-35250342012-12-21 The study of CD117 expression in glial tumors and its relationship with the tumor-type and grade Mahzouni, Parvin Jafari, Mohsen J Res Med Sci Original Article BACKGROUND: CD117 is a thyrosin kinase receptor encoded by c-kit proto-oncogene. It is expressed during normal development in some tissues and also in a subset of neoplasia especially gastrointestinal stromal tumors (GISTs). Treatment with thyrosin kinase inhibitors (e.g., Imatinib) is useful in CD117- positive GISTs. The goal of this study is to investigate the expression of CD117 in glial tumors as a potential diagnostic marker and target for therapy. MATERIALS AND METHODS: in this descriptive-analytical study, paraffin- embedded tissue blocks from 50 cases of glial tumors (various histological types and grades) were selected in a convenience sampling for the CD117 immunhistochemical study including expression of the marker, staining intensity, and percentage of the stained cells. The results were analyzed by Chi-square and Mann–Whitney tests. RESULTS: CD117 expression was detected in about 76% of glial tumors but the frequency of the expression showed no statistically significant relationship with the tumor type (P = 0.829). Although CD117 immunoreactivity was more frequent in high-grade tumors (84%) compared to the low-grade ones (68%), no statistically significant relationship was found between the CD117 expression and grade of the tumor (P = 0.09). Staining intensity and percentage of stained cells in high-grade tumors were significantly more than in low-grade tumors (P values of 0.046 and 0.023, respectively). CONCLUSION: according to the statistically significant difference in the staining intensity and percentage of the stained cells between the low-grade and high-grade glial tumors, these two parameters may be useful for making distinction between various grades of these tumors. Moreover, according to the prominent expression of CD117 in high-grade gliomas, these tumors may be potential candidates for treatment with thyrosin kinase inhibitors. Medknow Publications & Media Pvt Ltd 2012-02 /pmc/articles/PMC3525034/ /pubmed/23264790 Text en Copyright: © Journal of Research in Medical Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Mahzouni, Parvin
Jafari, Mohsen
The study of CD117 expression in glial tumors and its relationship with the tumor-type and grade
title The study of CD117 expression in glial tumors and its relationship with the tumor-type and grade
title_full The study of CD117 expression in glial tumors and its relationship with the tumor-type and grade
title_fullStr The study of CD117 expression in glial tumors and its relationship with the tumor-type and grade
title_full_unstemmed The study of CD117 expression in glial tumors and its relationship with the tumor-type and grade
title_short The study of CD117 expression in glial tumors and its relationship with the tumor-type and grade
title_sort study of cd117 expression in glial tumors and its relationship with the tumor-type and grade
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3525034/
https://www.ncbi.nlm.nih.gov/pubmed/23264790
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