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The immunoexpression of epidermal growth factor receptor in cutaneous squamous cell carcinoma

Although cutaneous squamous cell carcinomas (cSCCs) account for only 20–25% of non-melanoma skin cancers (NMSCs), they are responsible for most deaths attributable to NMSCs. Apart from SCC seric level, which increases in late-stage disease, no other predictive biomarker for cSCC exists. Epidermal gr...

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Autores principales: Nichita, Mirela Marcela, Giurcăneanu, Călin, Mihai, Mara Mădălina, Ghigulescu, Mihaela, Beiu, Cristina, Negoiţă, Silvius Ioan, Popa, Liliana Gabriela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academy of Medical Sciences, Romanian Academy Publishing House, Bucharest 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8597383/
https://www.ncbi.nlm.nih.gov/pubmed/34609422
http://dx.doi.org/10.47162/RJME.62.1.19
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author Nichita, Mirela Marcela
Giurcăneanu, Călin
Mihai, Mara Mădălina
Ghigulescu, Mihaela
Beiu, Cristina
Negoiţă, Silvius Ioan
Popa, Liliana Gabriela
author_facet Nichita, Mirela Marcela
Giurcăneanu, Călin
Mihai, Mara Mădălina
Ghigulescu, Mihaela
Beiu, Cristina
Negoiţă, Silvius Ioan
Popa, Liliana Gabriela
author_sort Nichita, Mirela Marcela
collection PubMed
description Although cutaneous squamous cell carcinomas (cSCCs) account for only 20–25% of non-melanoma skin cancers (NMSCs), they are responsible for most deaths attributable to NMSCs. Apart from SCC seric level, which increases in late-stage disease, no other predictive biomarker for cSCC exists. Epidermal growth factor receptor (EGFR) serves as a predictive biomarker and therapeutic target in numerous malignancies. EGFR immunoexpression is highly elevated in head and neck mucosal SCC. However, its immunoexpression pattern, its relationship with prognosis and survival, and the effect of EGFR targeted therapy in advanced cSCC have not been clarified. We assessed EGFR immunoexpression in 18 cases of cSCC and correlated our findings with the clinicopathological features. Immunohistochemical stainings with anti-EGFR monoclonal antibodies were practiced and the membrane and cytoplasmic immunostaining intensity and quality in the tumors and the non-lesional epithelium were analyzed. Membrane EGFR immunoexpression within the tumors increased with the tumor grade. EGFR overexpression was more frequently found in head and neck cSCCs. We did not find a direct relationship between cytoplasmic EGFR immunoexpression and clinicopathological findings and prognosis. Our results confirm that increased EGFR immunoexpression correlates with aggressive cSCC phenotypes and underline the need for novel treatments for these patients.
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spelling pubmed-85973832021-12-01 The immunoexpression of epidermal growth factor receptor in cutaneous squamous cell carcinoma Nichita, Mirela Marcela Giurcăneanu, Călin Mihai, Mara Mădălina Ghigulescu, Mihaela Beiu, Cristina Negoiţă, Silvius Ioan Popa, Liliana Gabriela Rom J Morphol Embryol Original Paper Although cutaneous squamous cell carcinomas (cSCCs) account for only 20–25% of non-melanoma skin cancers (NMSCs), they are responsible for most deaths attributable to NMSCs. Apart from SCC seric level, which increases in late-stage disease, no other predictive biomarker for cSCC exists. Epidermal growth factor receptor (EGFR) serves as a predictive biomarker and therapeutic target in numerous malignancies. EGFR immunoexpression is highly elevated in head and neck mucosal SCC. However, its immunoexpression pattern, its relationship with prognosis and survival, and the effect of EGFR targeted therapy in advanced cSCC have not been clarified. We assessed EGFR immunoexpression in 18 cases of cSCC and correlated our findings with the clinicopathological features. Immunohistochemical stainings with anti-EGFR monoclonal antibodies were practiced and the membrane and cytoplasmic immunostaining intensity and quality in the tumors and the non-lesional epithelium were analyzed. Membrane EGFR immunoexpression within the tumors increased with the tumor grade. EGFR overexpression was more frequently found in head and neck cSCCs. We did not find a direct relationship between cytoplasmic EGFR immunoexpression and clinicopathological findings and prognosis. Our results confirm that increased EGFR immunoexpression correlates with aggressive cSCC phenotypes and underline the need for novel treatments for these patients. Academy of Medical Sciences, Romanian Academy Publishing House, Bucharest 2021 2021-08-31 /pmc/articles/PMC8597383/ /pubmed/34609422 http://dx.doi.org/10.47162/RJME.62.1.19 Text en Copyright © 2020, Academy of Medical Sciences, Romanian Academy Publishing House, Bucharest https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open-access article distributed under the terms of a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Public License, which permits unrestricted use, adaptation, distribution and reproduction in any medium, non-commercially, provided the new creations are licensed under identical terms as the original work and the original work is properly cited.
spellingShingle Original Paper
Nichita, Mirela Marcela
Giurcăneanu, Călin
Mihai, Mara Mădălina
Ghigulescu, Mihaela
Beiu, Cristina
Negoiţă, Silvius Ioan
Popa, Liliana Gabriela
The immunoexpression of epidermal growth factor receptor in cutaneous squamous cell carcinoma
title The immunoexpression of epidermal growth factor receptor in cutaneous squamous cell carcinoma
title_full The immunoexpression of epidermal growth factor receptor in cutaneous squamous cell carcinoma
title_fullStr The immunoexpression of epidermal growth factor receptor in cutaneous squamous cell carcinoma
title_full_unstemmed The immunoexpression of epidermal growth factor receptor in cutaneous squamous cell carcinoma
title_short The immunoexpression of epidermal growth factor receptor in cutaneous squamous cell carcinoma
title_sort immunoexpression of epidermal growth factor receptor in cutaneous squamous cell carcinoma
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8597383/
https://www.ncbi.nlm.nih.gov/pubmed/34609422
http://dx.doi.org/10.47162/RJME.62.1.19
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