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Expression of HER-2/neu in Oral Squamous Cell Carcinoma

BACKGROUND: HER-2/neu is a member of the human epidermal growth factor (HER) family of transmembrane tyrosine kinases, which is significantly associated with the pathogenesis of various cancer types. The aim was to evaluate the expression of HER-2/neu in oral squamous cell carcinoma (OSCC) as a pote...

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Autores principales: Mirza, Sana, Hadi, Naila, Pervaiz, Shahid, Khan, Sultan Zeb, Mokeem, Sameer A, Abduljabbar, Tariq, Al-Hamoudi, Nawwaf, Vohra, Fahim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: West Asia Organization for Cancer Prevention 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7541867/
https://www.ncbi.nlm.nih.gov/pubmed/32458657
http://dx.doi.org/10.31557/APJCP.2020.21.5.1465
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author Mirza, Sana
Hadi, Naila
Pervaiz, Shahid
Khan, Sultan Zeb
Mokeem, Sameer A
Abduljabbar, Tariq
Al-Hamoudi, Nawwaf
Vohra, Fahim
author_facet Mirza, Sana
Hadi, Naila
Pervaiz, Shahid
Khan, Sultan Zeb
Mokeem, Sameer A
Abduljabbar, Tariq
Al-Hamoudi, Nawwaf
Vohra, Fahim
author_sort Mirza, Sana
collection PubMed
description BACKGROUND: HER-2/neu is a member of the human epidermal growth factor (HER) family of transmembrane tyrosine kinases, which is significantly associated with the pathogenesis of various cancer types. The aim was to evaluate the expression of HER-2/neu in oral squamous cell carcinoma (OSCC) as a potential biomarker to target antigens for specific immunotherapy in OSCC. METHODS: One hundred and forty histologically diagnosed OSCC cases were identified. Four to five-micrometer thick formalin-fixed, paraffin-embedded tumor sections were stained with Haematoxylin and Eosin (H and E). Histological grade was assessed according to WHO/Broders classification, while tumors were staged according to the American Joint Committee on Cancer (AJCC) TNM classification from stage I to IV. Immunohistochemistry was performed by using Rabbit monoclonal antibody against HER-2/neu (EP700Y, cell marquee and diluted 1:50). FISH was performed on positive cases using Vysis PathVysion HER-2 DNA probe (Abbott USA). Probes consist of LSI HER gene spectrum orange and control probe CEP 17 spectrum green. RESULTS: In this study, males were mostly effected (64.3%) with buccal mucosa (49%) to be the commonly involved site for OSCC. Majority of cases were moderately differentiated (62.1%) and 50.7% tumors were Stage IV. HER-2/neu was found to be positive (2+) in one case of OSCC, however weak to moderate complete membrane staining was observed in >10% of the tumor cells. One hundred and thirty nine cases were HER-2/neu negative. FISH analysis of HER-2/neu positive cases also showed gene amplification (Her2-neu/ CEp 17 = 225/33 = 7.2). CONCLUSIONS: The study showed disparity in the expression of HER-2/neu in OSCC, which is due to multiple reasons. Therefore therapy against HER-2/neu in OSCC is debatable.
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spelling pubmed-75418672020-10-14 Expression of HER-2/neu in Oral Squamous Cell Carcinoma Mirza, Sana Hadi, Naila Pervaiz, Shahid Khan, Sultan Zeb Mokeem, Sameer A Abduljabbar, Tariq Al-Hamoudi, Nawwaf Vohra, Fahim Asian Pac J Cancer Prev Research Article BACKGROUND: HER-2/neu is a member of the human epidermal growth factor (HER) family of transmembrane tyrosine kinases, which is significantly associated with the pathogenesis of various cancer types. The aim was to evaluate the expression of HER-2/neu in oral squamous cell carcinoma (OSCC) as a potential biomarker to target antigens for specific immunotherapy in OSCC. METHODS: One hundred and forty histologically diagnosed OSCC cases were identified. Four to five-micrometer thick formalin-fixed, paraffin-embedded tumor sections were stained with Haematoxylin and Eosin (H and E). Histological grade was assessed according to WHO/Broders classification, while tumors were staged according to the American Joint Committee on Cancer (AJCC) TNM classification from stage I to IV. Immunohistochemistry was performed by using Rabbit monoclonal antibody against HER-2/neu (EP700Y, cell marquee and diluted 1:50). FISH was performed on positive cases using Vysis PathVysion HER-2 DNA probe (Abbott USA). Probes consist of LSI HER gene spectrum orange and control probe CEP 17 spectrum green. RESULTS: In this study, males were mostly effected (64.3%) with buccal mucosa (49%) to be the commonly involved site for OSCC. Majority of cases were moderately differentiated (62.1%) and 50.7% tumors were Stage IV. HER-2/neu was found to be positive (2+) in one case of OSCC, however weak to moderate complete membrane staining was observed in >10% of the tumor cells. One hundred and thirty nine cases were HER-2/neu negative. FISH analysis of HER-2/neu positive cases also showed gene amplification (Her2-neu/ CEp 17 = 225/33 = 7.2). CONCLUSIONS: The study showed disparity in the expression of HER-2/neu in OSCC, which is due to multiple reasons. Therefore therapy against HER-2/neu in OSCC is debatable. West Asia Organization for Cancer Prevention 2020-05 /pmc/articles/PMC7541867/ /pubmed/32458657 http://dx.doi.org/10.31557/APJCP.2020.21.5.1465 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 Research Article
Mirza, Sana
Hadi, Naila
Pervaiz, Shahid
Khan, Sultan Zeb
Mokeem, Sameer A
Abduljabbar, Tariq
Al-Hamoudi, Nawwaf
Vohra, Fahim
Expression of HER-2/neu in Oral Squamous Cell Carcinoma
title Expression of HER-2/neu in Oral Squamous Cell Carcinoma
title_full Expression of HER-2/neu in Oral Squamous Cell Carcinoma
title_fullStr Expression of HER-2/neu in Oral Squamous Cell Carcinoma
title_full_unstemmed Expression of HER-2/neu in Oral Squamous Cell Carcinoma
title_short Expression of HER-2/neu in Oral Squamous Cell Carcinoma
title_sort expression of her-2/neu in oral squamous cell carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7541867/
https://www.ncbi.nlm.nih.gov/pubmed/32458657
http://dx.doi.org/10.31557/APJCP.2020.21.5.1465
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