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Differences in actin expression between primary and recurrent facial basal cell carcinomas as a prognostic factor of local recurrence

INTRODUCTION: Due to a relatively high recurrence rate of facial basal cell carcinoma (BCC), its morbidity is very significant. AIM: To analyse the expression of α-SMA, E-cadherin, Ber-Ep4 and MOC-31 as predictors of local recurrence in a group of patients with primary and recurrent BCCs of the face...

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Autores principales: Iwulska, Katarzyna, Wyszyńska-Pawelec, Grażyna, Zapała, Jan, Kosowski, Bogdan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8330871/
https://www.ncbi.nlm.nih.gov/pubmed/34377133
http://dx.doi.org/10.5114/ada.2021.107935
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author Iwulska, Katarzyna
Wyszyńska-Pawelec, Grażyna
Zapała, Jan
Kosowski, Bogdan
author_facet Iwulska, Katarzyna
Wyszyńska-Pawelec, Grażyna
Zapała, Jan
Kosowski, Bogdan
author_sort Iwulska, Katarzyna
collection PubMed
description INTRODUCTION: Due to a relatively high recurrence rate of facial basal cell carcinoma (BCC), its morbidity is very significant. AIM: To analyse the expression of α-SMA, E-cadherin, Ber-Ep4 and MOC-31 as predictors of local recurrence in a group of patients with primary and recurrent BCCs of the face in correlation with histological and clinical data. MATERIAL AND METHODS: The study cohort included 79 patients with facial BCC (52 with primary BCC and 27 with recurrent BCC) who were treated at the Department of Cranio-Maxillofacial Surgery of the Jagiellonian University, Krakow in 1997–2009. RESULTS: Significant risk factors for local recurrence included: recurrent tumour (p = 0.001), multifocal BCC (p = 0.01), incomplete tumour excision (p = 0.02) and the aggressive infiltrating histologic subtype of BCC (p = 0.05). In the group of primary BCCs, positive expression of stromal α-SMA (p = 0.03) correlated with a statistically significant higher recurrence rate and so did positive expression of α-SMA in tumour cells of recurrent BCC (p = 0.002). In the group of primary aggressive BCC subtypes, reduced expression of MOC-31 was also associated with a higher rate of relapse (p = 0.02). CONCLUSIONS: Our findings provide information about α-SMA and MOC-31 expression in primary and recurrent BCCs. These data may contribute to the formulation of a more targeted treatment plan and follow-up strategy for patients with facial basal cell carcinoma.
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spelling pubmed-83308712021-08-09 Differences in actin expression between primary and recurrent facial basal cell carcinomas as a prognostic factor of local recurrence Iwulska, Katarzyna Wyszyńska-Pawelec, Grażyna Zapała, Jan Kosowski, Bogdan Postepy Dermatol Alergol Original Paper INTRODUCTION: Due to a relatively high recurrence rate of facial basal cell carcinoma (BCC), its morbidity is very significant. AIM: To analyse the expression of α-SMA, E-cadherin, Ber-Ep4 and MOC-31 as predictors of local recurrence in a group of patients with primary and recurrent BCCs of the face in correlation with histological and clinical data. MATERIAL AND METHODS: The study cohort included 79 patients with facial BCC (52 with primary BCC and 27 with recurrent BCC) who were treated at the Department of Cranio-Maxillofacial Surgery of the Jagiellonian University, Krakow in 1997–2009. RESULTS: Significant risk factors for local recurrence included: recurrent tumour (p = 0.001), multifocal BCC (p = 0.01), incomplete tumour excision (p = 0.02) and the aggressive infiltrating histologic subtype of BCC (p = 0.05). In the group of primary BCCs, positive expression of stromal α-SMA (p = 0.03) correlated with a statistically significant higher recurrence rate and so did positive expression of α-SMA in tumour cells of recurrent BCC (p = 0.002). In the group of primary aggressive BCC subtypes, reduced expression of MOC-31 was also associated with a higher rate of relapse (p = 0.02). CONCLUSIONS: Our findings provide information about α-SMA and MOC-31 expression in primary and recurrent BCCs. These data may contribute to the formulation of a more targeted treatment plan and follow-up strategy for patients with facial basal cell carcinoma. Termedia Publishing House 2021-07-26 2021-06 /pmc/articles/PMC8330871/ /pubmed/34377133 http://dx.doi.org/10.5114/ada.2021.107935 Text en Copyright: © 2021 Termedia Sp. z o. o. https://creativecommons.org/licenses/by-nc-sa/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Original Paper
Iwulska, Katarzyna
Wyszyńska-Pawelec, Grażyna
Zapała, Jan
Kosowski, Bogdan
Differences in actin expression between primary and recurrent facial basal cell carcinomas as a prognostic factor of local recurrence
title Differences in actin expression between primary and recurrent facial basal cell carcinomas as a prognostic factor of local recurrence
title_full Differences in actin expression between primary and recurrent facial basal cell carcinomas as a prognostic factor of local recurrence
title_fullStr Differences in actin expression between primary and recurrent facial basal cell carcinomas as a prognostic factor of local recurrence
title_full_unstemmed Differences in actin expression between primary and recurrent facial basal cell carcinomas as a prognostic factor of local recurrence
title_short Differences in actin expression between primary and recurrent facial basal cell carcinomas as a prognostic factor of local recurrence
title_sort differences in actin expression between primary and recurrent facial basal cell carcinomas as a prognostic factor of local recurrence
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8330871/
https://www.ncbi.nlm.nih.gov/pubmed/34377133
http://dx.doi.org/10.5114/ada.2021.107935
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