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Immunohistochemical Expression of MMP-9 and E-Cadherin in subtypes of Ameloblastoma

BACKGROUND & OBJECTIVE: Ameloblastomas have been analyzed histologically for diagnostics and its sub-classification; however, the analysis carried out so far does not provide any authentic evidence regarding prognosis of Ameloblastoma. Subject categorization is still a topic of debate. The purpo...

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Autores principales: Farhan, Farah, Niazi, Zainab, Masood, Sana, Abbas, Beenish
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Professional Medical Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8713232/
https://www.ncbi.nlm.nih.gov/pubmed/35035427
http://dx.doi.org/10.12669/pjms.38.1.4465
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author Farhan, Farah
Niazi, Zainab
Masood, Sana
Abbas, Beenish
author_facet Farhan, Farah
Niazi, Zainab
Masood, Sana
Abbas, Beenish
author_sort Farhan, Farah
collection PubMed
description BACKGROUND & OBJECTIVE: Ameloblastomas have been analyzed histologically for diagnostics and its sub-classification; however, the analysis carried out so far does not provide any authentic evidence regarding prognosis of Ameloblastoma. Subject categorization is still a topic of debate. The purpose of this study was to determine the immuno-expression of markers such as MMP-9 and E-Cadherin in different sub-types of ameloblastoma and establish their correlation with histological variants. METHODS: Analytical study of 71 cases of ameloblastoma was conducted in AFIP Rawalpindi, between January to June, 2019. Samples were taken from different intraoral sites including the patients with tumor of ameloblast. The tumor was sub classified histologically on the basis of WHO classification. ‘Chi Square’ Test was applied to find the association of MMP-9 and E-Cadherin with histological variants of ameloblastoma. P-value ≤ 0.05 were found statistically significant. RESULTS: On histopathological sub-classification, 52.1% were diagnosed as follicular type, 23.9% were plexiform type, 14.1% were Acanthomatous type and 9.9% were of unicystic ameloblastoma. 80% of the total Acanthomatous type and 59% of the total plexiform had strong immuno-expression, which was significantly different from follicular type MMP-9 (p ≤ 0.05). All cases of unicystic ameloblastoma and 67.6% of follicular type showed strong immuno-expression significantly different from 20% of Acanthomatous type and 59% of plexiform type E-Cadherin (p ≥ 0.05). On the other hand, when statistical analysis was carried out, an inverse relation between MMP-9 and E-cadherin was observed. CONCLUSION: The effect of MMP-9 and E-cadherin in ameloblastoma is aggressive in nature and effectiveness was seen in subtypes of ameloblastoma.
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spelling pubmed-87132322022-01-13 Immunohistochemical Expression of MMP-9 and E-Cadherin in subtypes of Ameloblastoma Farhan, Farah Niazi, Zainab Masood, Sana Abbas, Beenish Pak J Med Sci Original Article BACKGROUND & OBJECTIVE: Ameloblastomas have been analyzed histologically for diagnostics and its sub-classification; however, the analysis carried out so far does not provide any authentic evidence regarding prognosis of Ameloblastoma. Subject categorization is still a topic of debate. The purpose of this study was to determine the immuno-expression of markers such as MMP-9 and E-Cadherin in different sub-types of ameloblastoma and establish their correlation with histological variants. METHODS: Analytical study of 71 cases of ameloblastoma was conducted in AFIP Rawalpindi, between January to June, 2019. Samples were taken from different intraoral sites including the patients with tumor of ameloblast. The tumor was sub classified histologically on the basis of WHO classification. ‘Chi Square’ Test was applied to find the association of MMP-9 and E-Cadherin with histological variants of ameloblastoma. P-value ≤ 0.05 were found statistically significant. RESULTS: On histopathological sub-classification, 52.1% were diagnosed as follicular type, 23.9% were plexiform type, 14.1% were Acanthomatous type and 9.9% were of unicystic ameloblastoma. 80% of the total Acanthomatous type and 59% of the total plexiform had strong immuno-expression, which was significantly different from follicular type MMP-9 (p ≤ 0.05). All cases of unicystic ameloblastoma and 67.6% of follicular type showed strong immuno-expression significantly different from 20% of Acanthomatous type and 59% of plexiform type E-Cadherin (p ≥ 0.05). On the other hand, when statistical analysis was carried out, an inverse relation between MMP-9 and E-cadherin was observed. CONCLUSION: The effect of MMP-9 and E-cadherin in ameloblastoma is aggressive in nature and effectiveness was seen in subtypes of ameloblastoma. Professional Medical Publications 2022 /pmc/articles/PMC8713232/ /pubmed/35035427 http://dx.doi.org/10.12669/pjms.38.1.4465 Text en Copyright: © Pakistan Journal of Medical Sciences https://creativecommons.org/licenses/by/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0 (https://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
Farhan, Farah
Niazi, Zainab
Masood, Sana
Abbas, Beenish
Immunohistochemical Expression of MMP-9 and E-Cadherin in subtypes of Ameloblastoma
title Immunohistochemical Expression of MMP-9 and E-Cadherin in subtypes of Ameloblastoma
title_full Immunohistochemical Expression of MMP-9 and E-Cadherin in subtypes of Ameloblastoma
title_fullStr Immunohistochemical Expression of MMP-9 and E-Cadherin in subtypes of Ameloblastoma
title_full_unstemmed Immunohistochemical Expression of MMP-9 and E-Cadherin in subtypes of Ameloblastoma
title_short Immunohistochemical Expression of MMP-9 and E-Cadherin in subtypes of Ameloblastoma
title_sort immunohistochemical expression of mmp-9 and e-cadherin in subtypes of ameloblastoma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8713232/
https://www.ncbi.nlm.nih.gov/pubmed/35035427
http://dx.doi.org/10.12669/pjms.38.1.4465
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