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Immunohistochemical detection of the chondroitin sulfate proteoglycan 4 protein in primary and metastatic melanoma

Treatment of malignant melanoma, the most aggressive form of skin cancer, continues to be a major challenge for clinicians. New targeted therapies with kinase inhibitors or drugs which modify the immune response are often accompanied by the development of resistance or severe side effects. In this c...

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Autores principales: Grossauer, Anna, Uranowska, Karolina, Kitzwögerer, Melitta, Mostegel, Margit, Breiteneder, Heimo, Hafner, Christine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10407859/
https://www.ncbi.nlm.nih.gov/pubmed/37559576
http://dx.doi.org/10.3892/ol.2023.13968
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author Grossauer, Anna
Uranowska, Karolina
Kitzwögerer, Melitta
Mostegel, Margit
Breiteneder, Heimo
Hafner, Christine
author_facet Grossauer, Anna
Uranowska, Karolina
Kitzwögerer, Melitta
Mostegel, Margit
Breiteneder, Heimo
Hafner, Christine
author_sort Grossauer, Anna
collection PubMed
description Treatment of malignant melanoma, the most aggressive form of skin cancer, continues to be a major challenge for clinicians. New targeted therapies with kinase inhibitors or drugs which modify the immune response are often accompanied by the development of resistance or severe side effects. In this context, chondroitin sulfate proteoglycan 4 (CSPG4), a highly immunogenic melanoma tumor antigen, could be a potential target for alternative therapeutic approaches. The aim of the present study was to identify differences in the levels of CSPG4 protein expression in primary and metastatic melanomas as well as to analyze correlations between CSPG4 expression and histopathological data and patient characteristics. A total of 189 melanoma tissue samples from Lower Austria, including primary melanomas and melanoma metastases, were immunohistochemically stained for the expression of CSPG4 and statistical analyses were performed. A total of 65.6% of melanoma tissue samples stained positive for the expression of CSPG4. Primary nodular and primary superficial spreading melanomas demonstrated a significantly higher number of positively stained tissue samples for CSPG4 compared with primary lentigo maligna melanomas. No significant differences in the expression of CSPG4 were demonstrated between primary melanomas and melanoma metastases. The present study supports the advancement of the understanding of CSPG4 tissue expression patterns in melanoma patients and provides additional information for further investigation of CSPG4 as a potential therapeutic target.
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spelling pubmed-104078592023-08-09 Immunohistochemical detection of the chondroitin sulfate proteoglycan 4 protein in primary and metastatic melanoma Grossauer, Anna Uranowska, Karolina Kitzwögerer, Melitta Mostegel, Margit Breiteneder, Heimo Hafner, Christine Oncol Lett Articles Treatment of malignant melanoma, the most aggressive form of skin cancer, continues to be a major challenge for clinicians. New targeted therapies with kinase inhibitors or drugs which modify the immune response are often accompanied by the development of resistance or severe side effects. In this context, chondroitin sulfate proteoglycan 4 (CSPG4), a highly immunogenic melanoma tumor antigen, could be a potential target for alternative therapeutic approaches. The aim of the present study was to identify differences in the levels of CSPG4 protein expression in primary and metastatic melanomas as well as to analyze correlations between CSPG4 expression and histopathological data and patient characteristics. A total of 189 melanoma tissue samples from Lower Austria, including primary melanomas and melanoma metastases, were immunohistochemically stained for the expression of CSPG4 and statistical analyses were performed. A total of 65.6% of melanoma tissue samples stained positive for the expression of CSPG4. Primary nodular and primary superficial spreading melanomas demonstrated a significantly higher number of positively stained tissue samples for CSPG4 compared with primary lentigo maligna melanomas. No significant differences in the expression of CSPG4 were demonstrated between primary melanomas and melanoma metastases. The present study supports the advancement of the understanding of CSPG4 tissue expression patterns in melanoma patients and provides additional information for further investigation of CSPG4 as a potential therapeutic target. D.A. Spandidos 2023-07-20 /pmc/articles/PMC10407859/ /pubmed/37559576 http://dx.doi.org/10.3892/ol.2023.13968 Text en Copyright: © Grossauer et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Grossauer, Anna
Uranowska, Karolina
Kitzwögerer, Melitta
Mostegel, Margit
Breiteneder, Heimo
Hafner, Christine
Immunohistochemical detection of the chondroitin sulfate proteoglycan 4 protein in primary and metastatic melanoma
title Immunohistochemical detection of the chondroitin sulfate proteoglycan 4 protein in primary and metastatic melanoma
title_full Immunohistochemical detection of the chondroitin sulfate proteoglycan 4 protein in primary and metastatic melanoma
title_fullStr Immunohistochemical detection of the chondroitin sulfate proteoglycan 4 protein in primary and metastatic melanoma
title_full_unstemmed Immunohistochemical detection of the chondroitin sulfate proteoglycan 4 protein in primary and metastatic melanoma
title_short Immunohistochemical detection of the chondroitin sulfate proteoglycan 4 protein in primary and metastatic melanoma
title_sort immunohistochemical detection of the chondroitin sulfate proteoglycan 4 protein in primary and metastatic melanoma
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10407859/
https://www.ncbi.nlm.nih.gov/pubmed/37559576
http://dx.doi.org/10.3892/ol.2023.13968
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