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The diagnostic importance of matrix metalloproteinase-7 and nestin in gastrointestinal stromal tumors
BACKGROUND: The importance of the matrix metalloproteinase-7 (MMP-7) and nestin immunomarkers, C-kit proto-oncogene (CD117), and the efficiency of the Ki-67 proliferation index for gastrointestinal stromal tumors were evaluated. MATERIAL/METHODS: This study was conducted by examining the microscope...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4005864/ https://www.ncbi.nlm.nih.gov/pubmed/24755685 http://dx.doi.org/10.12659/MSM.890303 |
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author | Peker, Kemal Sayar, Ilyas Gelincik, İbrahim Bulut, Gülay Ünal, Tuba Dilay Kökenek Şenol, Serkan Gökçe, Aysun Isik, Arda |
author_facet | Peker, Kemal Sayar, Ilyas Gelincik, İbrahim Bulut, Gülay Ünal, Tuba Dilay Kökenek Şenol, Serkan Gökçe, Aysun Isik, Arda |
author_sort | Peker, Kemal |
collection | PubMed |
description | BACKGROUND: The importance of the matrix metalloproteinase-7 (MMP-7) and nestin immunomarkers, C-kit proto-oncogene (CD117), and the efficiency of the Ki-67 proliferation index for gastrointestinal stromal tumors were evaluated. MATERIAL/METHODS: This study was conducted by examining the microscope slides of 72 patients with gastrointestinal stromal tumors that were sent to the pathology laboratory between 2007 and 2012. Immunohistochemical staining for CD117, MMP-7, nestin, and marker of proliferation Ki-67 was performed. The correlations between the positive results for Ki-67, CD117, MMP-7, and nestin were evaluated relative to the tumor characteristics of size, localization, grade, cellular type, cellularity, cytology type, growth pattern, ulceration, necrosis, hemorrhage, invasion depth, and lymph node metastasis. RESULTS: The tumor was localized in the stomach in 42 of the patients, the intestines in 19, the colon in 7, and the rectum in 4. Comparisons among the groups showed that MMP-7 was correlated with the tumor grade (p<0.001), cellularity (p<0.009), cytologic atypia (p<0.001), ulceration (p=0.002), necrosis (p<0.001), and tumor size (p=0.001). Nestin was correlated with the tumor grade (p=0.013), and tumor size (p=0.024). Correlations among CD117, MMP-7, nestin, and Ki-67 were examined. Nestin and Ki-67 were both significantly correlated with CD117 and MMP-7 [(r=0.279, p=0.018), (r=0.322, p=0.006), (r=0.386, p=0.001), (r=0.386, p=0.002)], respectively. CONCLUSIONS: MMP-7 and nestin may be beneficial as markers, given their sensitivity to gastrointestinal stromal tumors. |
format | Online Article Text |
id | pubmed-4005864 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | International Scientific Literature, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-40058642014-05-01 The diagnostic importance of matrix metalloproteinase-7 and nestin in gastrointestinal stromal tumors Peker, Kemal Sayar, Ilyas Gelincik, İbrahim Bulut, Gülay Ünal, Tuba Dilay Kökenek Şenol, Serkan Gökçe, Aysun Isik, Arda Med Sci Monit Lab/In Vitro Research BACKGROUND: The importance of the matrix metalloproteinase-7 (MMP-7) and nestin immunomarkers, C-kit proto-oncogene (CD117), and the efficiency of the Ki-67 proliferation index for gastrointestinal stromal tumors were evaluated. MATERIAL/METHODS: This study was conducted by examining the microscope slides of 72 patients with gastrointestinal stromal tumors that were sent to the pathology laboratory between 2007 and 2012. Immunohistochemical staining for CD117, MMP-7, nestin, and marker of proliferation Ki-67 was performed. The correlations between the positive results for Ki-67, CD117, MMP-7, and nestin were evaluated relative to the tumor characteristics of size, localization, grade, cellular type, cellularity, cytology type, growth pattern, ulceration, necrosis, hemorrhage, invasion depth, and lymph node metastasis. RESULTS: The tumor was localized in the stomach in 42 of the patients, the intestines in 19, the colon in 7, and the rectum in 4. Comparisons among the groups showed that MMP-7 was correlated with the tumor grade (p<0.001), cellularity (p<0.009), cytologic atypia (p<0.001), ulceration (p=0.002), necrosis (p<0.001), and tumor size (p=0.001). Nestin was correlated with the tumor grade (p=0.013), and tumor size (p=0.024). Correlations among CD117, MMP-7, nestin, and Ki-67 were examined. Nestin and Ki-67 were both significantly correlated with CD117 and MMP-7 [(r=0.279, p=0.018), (r=0.322, p=0.006), (r=0.386, p=0.001), (r=0.386, p=0.002)], respectively. CONCLUSIONS: MMP-7 and nestin may be beneficial as markers, given their sensitivity to gastrointestinal stromal tumors. International Scientific Literature, Inc. 2014-04-23 /pmc/articles/PMC4005864/ /pubmed/24755685 http://dx.doi.org/10.12659/MSM.890303 Text en © Med Sci Monit, 2014 This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License |
spellingShingle | Lab/In Vitro Research Peker, Kemal Sayar, Ilyas Gelincik, İbrahim Bulut, Gülay Ünal, Tuba Dilay Kökenek Şenol, Serkan Gökçe, Aysun Isik, Arda The diagnostic importance of matrix metalloproteinase-7 and nestin in gastrointestinal stromal tumors |
title | The diagnostic importance of matrix metalloproteinase-7 and nestin in gastrointestinal stromal tumors |
title_full | The diagnostic importance of matrix metalloproteinase-7 and nestin in gastrointestinal stromal tumors |
title_fullStr | The diagnostic importance of matrix metalloproteinase-7 and nestin in gastrointestinal stromal tumors |
title_full_unstemmed | The diagnostic importance of matrix metalloproteinase-7 and nestin in gastrointestinal stromal tumors |
title_short | The diagnostic importance of matrix metalloproteinase-7 and nestin in gastrointestinal stromal tumors |
title_sort | diagnostic importance of matrix metalloproteinase-7 and nestin in gastrointestinal stromal tumors |
topic | Lab/In Vitro Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4005864/ https://www.ncbi.nlm.nih.gov/pubmed/24755685 http://dx.doi.org/10.12659/MSM.890303 |
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