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Immunoexpression of Bmi-1, CK15, Bcl-2 in different types of basal cell carcinomas

INTRODUCTION: Basal cell carcinoma (BCC) occurs in aggressive and non-aggressive forms. The expression of immunohistochemical markers varies in different types of BCC. AIM: Immunohistochemical analysis of selected proteins in BCCs. MATERIAL AND METHODS: The immunohistochemical method was used to exa...

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Autores principales: Iljin, Aleksandra, Stasikowska-Kanicka, Olga, Zieliñski, Tomasz, Bąkiewicz, Anna, Sporny, Stanisław, Woźniak-Roszkowska, Ewa, Antoszewski, Bogusław
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9704448/
https://www.ncbi.nlm.nih.gov/pubmed/36457690
http://dx.doi.org/10.5114/ada.2022.120888
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author Iljin, Aleksandra
Stasikowska-Kanicka, Olga
Zieliñski, Tomasz
Bąkiewicz, Anna
Sporny, Stanisław
Woźniak-Roszkowska, Ewa
Antoszewski, Bogusław
author_facet Iljin, Aleksandra
Stasikowska-Kanicka, Olga
Zieliñski, Tomasz
Bąkiewicz, Anna
Sporny, Stanisław
Woźniak-Roszkowska, Ewa
Antoszewski, Bogusław
author_sort Iljin, Aleksandra
collection PubMed
description INTRODUCTION: Basal cell carcinoma (BCC) occurs in aggressive and non-aggressive forms. The expression of immunohistochemical markers varies in different types of BCC. AIM: Immunohistochemical analysis of selected proteins in BCCs. MATERIAL AND METHODS: The immunohistochemical method was used to examine the immunoexpression of Bmi-1, CK15 and Bcl-2 in 56 cases of BCC divided into four groups. RESULTS: Positive Bmi-1 staining 3–4+ level (nodular type) was seen in 91.3% of samples, 4+ (infiltrative) in 92.3%, 4+ (nodular/infiltrative) – 69.2%, 3+ – 30.8%, in BSC 3+ – 42.8%, and 28.6% each for 2+ and 4+. Low grade positivity (0–1+) in CK15 staining was present in 52.1% of nodular BCC, 46.2% – nodular/infiltrative, 92.3% – infiltrative, and 100% – BSC, but levels 2–3+ in nodular BCC in 47.8%, nodular/infiltrative BCC – 53.8%, infiltrative – 7.7%. Bcl-2 positivity (3–4+) was revealed in nodular BCC in 95.6%, (1–2+) in 100% of BSC, infiltrative and infiltrative/nodular BCC, but the lowest (0–1+) in 76.9% of nodular/infiltrative BCC, 71.4% of BSC, and in 38.4% of infiltrative BCC. CONCLUSIONS: Positive Bmi-1 staining was the highest in the aggressive infiltrative subtype of BCCs, whereas the lowest in basosquamous cell carcinomas (BSC). Infiltrative BCC was characterized by a lower level of CK15 expression than nodular BCC and nodular/infiltrative BCC. Differentiation of Bcl-2 expression depended on the type of tumour; the highest level was found in nodular BCC, low grade in nodular/infiltrative and infiltrative BCCs, and BSC.
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spelling pubmed-97044482022-11-30 Immunoexpression of Bmi-1, CK15, Bcl-2 in different types of basal cell carcinomas Iljin, Aleksandra Stasikowska-Kanicka, Olga Zieliñski, Tomasz Bąkiewicz, Anna Sporny, Stanisław Woźniak-Roszkowska, Ewa Antoszewski, Bogusław Postepy Dermatol Alergol Original Paper INTRODUCTION: Basal cell carcinoma (BCC) occurs in aggressive and non-aggressive forms. The expression of immunohistochemical markers varies in different types of BCC. AIM: Immunohistochemical analysis of selected proteins in BCCs. MATERIAL AND METHODS: The immunohistochemical method was used to examine the immunoexpression of Bmi-1, CK15 and Bcl-2 in 56 cases of BCC divided into four groups. RESULTS: Positive Bmi-1 staining 3–4+ level (nodular type) was seen in 91.3% of samples, 4+ (infiltrative) in 92.3%, 4+ (nodular/infiltrative) – 69.2%, 3+ – 30.8%, in BSC 3+ – 42.8%, and 28.6% each for 2+ and 4+. Low grade positivity (0–1+) in CK15 staining was present in 52.1% of nodular BCC, 46.2% – nodular/infiltrative, 92.3% – infiltrative, and 100% – BSC, but levels 2–3+ in nodular BCC in 47.8%, nodular/infiltrative BCC – 53.8%, infiltrative – 7.7%. Bcl-2 positivity (3–4+) was revealed in nodular BCC in 95.6%, (1–2+) in 100% of BSC, infiltrative and infiltrative/nodular BCC, but the lowest (0–1+) in 76.9% of nodular/infiltrative BCC, 71.4% of BSC, and in 38.4% of infiltrative BCC. CONCLUSIONS: Positive Bmi-1 staining was the highest in the aggressive infiltrative subtype of BCCs, whereas the lowest in basosquamous cell carcinomas (BSC). Infiltrative BCC was characterized by a lower level of CK15 expression than nodular BCC and nodular/infiltrative BCC. Differentiation of Bcl-2 expression depended on the type of tumour; the highest level was found in nodular BCC, low grade in nodular/infiltrative and infiltrative BCCs, and BSC. Termedia Publishing House 2022-11-09 2022-10 /pmc/articles/PMC9704448/ /pubmed/36457690 http://dx.doi.org/10.5114/ada.2022.120888 Text en Copyright: © 2022 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
Iljin, Aleksandra
Stasikowska-Kanicka, Olga
Zieliñski, Tomasz
Bąkiewicz, Anna
Sporny, Stanisław
Woźniak-Roszkowska, Ewa
Antoszewski, Bogusław
Immunoexpression of Bmi-1, CK15, Bcl-2 in different types of basal cell carcinomas
title Immunoexpression of Bmi-1, CK15, Bcl-2 in different types of basal cell carcinomas
title_full Immunoexpression of Bmi-1, CK15, Bcl-2 in different types of basal cell carcinomas
title_fullStr Immunoexpression of Bmi-1, CK15, Bcl-2 in different types of basal cell carcinomas
title_full_unstemmed Immunoexpression of Bmi-1, CK15, Bcl-2 in different types of basal cell carcinomas
title_short Immunoexpression of Bmi-1, CK15, Bcl-2 in different types of basal cell carcinomas
title_sort immunoexpression of bmi-1, ck15, bcl-2 in different types of basal cell carcinomas
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9704448/
https://www.ncbi.nlm.nih.gov/pubmed/36457690
http://dx.doi.org/10.5114/ada.2022.120888
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