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Protein expression of prognostic genes in primary melanoma and benign nevi

PURPOSE: To evaluate the protein expression characteristics of genes employed in a recently introduced prognostic gene expression assay for patients with cutaneous melanoma (CM). METHODS: We studied 37 patients with CM and 10 with benign (melanocytic) nevi (BN). Immunohistochemistry of primary tumor...

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Autores principales: Gambichler, T., Elfering, J., Meyer, T., Bruckmüller, S., Stockfleth, E., Skrygan, M., Käfferlein, H. U., Brüning, T., Lang, K., Wagener, D., Schröder, S., Nick, M., Susok, L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9470607/
https://www.ncbi.nlm.nih.gov/pubmed/34757537
http://dx.doi.org/10.1007/s00432-021-03779-0
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author Gambichler, T.
Elfering, J.
Meyer, T.
Bruckmüller, S.
Stockfleth, E.
Skrygan, M.
Käfferlein, H. U.
Brüning, T.
Lang, K.
Wagener, D.
Schröder, S.
Nick, M.
Susok, L.
author_facet Gambichler, T.
Elfering, J.
Meyer, T.
Bruckmüller, S.
Stockfleth, E.
Skrygan, M.
Käfferlein, H. U.
Brüning, T.
Lang, K.
Wagener, D.
Schröder, S.
Nick, M.
Susok, L.
author_sort Gambichler, T.
collection PubMed
description PURPOSE: To evaluate the protein expression characteristics of genes employed in a recently introduced prognostic gene expression assay for patients with cutaneous melanoma (CM). METHODS: We studied 37 patients with CM and 10 with benign (melanocytic) nevi (BN). Immunohistochemistry of primary tumor tissue was performed for eight proteins: COL6A6, DCD, GBP4, KLHL41, KRT9, PIP, SCGB1D2, SCGB2A2. RESULTS: The protein expression of most markers investigated was relatively low (e.g., DCD, KRT9, SCGB1D2) and predominantly cytoplasmatic in melanocytes and keratinocytes. COL6A6, GBP4, and KLHL41 expression was significantly enhanced in CM when compared to BN. DCD protein expression was significantly correlated with COL6A6, GBP4, and KLHL41. GBP4 was positively correlated with KLHL41 and inversely correlated with SCGB2B2. The latter was also inversely correlated with serum S100B levels at time of initial diagnosis. The presence of SCGB1D2 expression was significantly associated with ulceration of the primary tumor. KRT9 protein expression was significantly more likely found in acral lentiginous melanoma. The presence of DCD expression was less likely associated with superficial spreading melanoma subtype but significantly associated with non-progressive disease. The absence of SCGB2A2 expression was significantly more often observed in patients who did not progress to stage III or IV. CONCLUSIONS: The expression levels observed were relatively low but differed in part with those found in BN. Even though we detected some significant correlations between the protein expression levels and clinical parameters (e.g., CM subtype, course of disease), there was no major concordance with the protective or risk-associated functions of the corresponding genes included in a recently introduced prognostic gene expression assay.
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spelling pubmed-94706072022-09-15 Protein expression of prognostic genes in primary melanoma and benign nevi Gambichler, T. Elfering, J. Meyer, T. Bruckmüller, S. Stockfleth, E. Skrygan, M. Käfferlein, H. U. Brüning, T. Lang, K. Wagener, D. Schröder, S. Nick, M. Susok, L. J Cancer Res Clin Oncol Original Article – Clinical Oncology PURPOSE: To evaluate the protein expression characteristics of genes employed in a recently introduced prognostic gene expression assay for patients with cutaneous melanoma (CM). METHODS: We studied 37 patients with CM and 10 with benign (melanocytic) nevi (BN). Immunohistochemistry of primary tumor tissue was performed for eight proteins: COL6A6, DCD, GBP4, KLHL41, KRT9, PIP, SCGB1D2, SCGB2A2. RESULTS: The protein expression of most markers investigated was relatively low (e.g., DCD, KRT9, SCGB1D2) and predominantly cytoplasmatic in melanocytes and keratinocytes. COL6A6, GBP4, and KLHL41 expression was significantly enhanced in CM when compared to BN. DCD protein expression was significantly correlated with COL6A6, GBP4, and KLHL41. GBP4 was positively correlated with KLHL41 and inversely correlated with SCGB2B2. The latter was also inversely correlated with serum S100B levels at time of initial diagnosis. The presence of SCGB1D2 expression was significantly associated with ulceration of the primary tumor. KRT9 protein expression was significantly more likely found in acral lentiginous melanoma. The presence of DCD expression was less likely associated with superficial spreading melanoma subtype but significantly associated with non-progressive disease. The absence of SCGB2A2 expression was significantly more often observed in patients who did not progress to stage III or IV. CONCLUSIONS: The expression levels observed were relatively low but differed in part with those found in BN. Even though we detected some significant correlations between the protein expression levels and clinical parameters (e.g., CM subtype, course of disease), there was no major concordance with the protective or risk-associated functions of the corresponding genes included in a recently introduced prognostic gene expression assay. Springer Berlin Heidelberg 2021-11-10 2022 /pmc/articles/PMC9470607/ /pubmed/34757537 http://dx.doi.org/10.1007/s00432-021-03779-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article – Clinical Oncology
Gambichler, T.
Elfering, J.
Meyer, T.
Bruckmüller, S.
Stockfleth, E.
Skrygan, M.
Käfferlein, H. U.
Brüning, T.
Lang, K.
Wagener, D.
Schröder, S.
Nick, M.
Susok, L.
Protein expression of prognostic genes in primary melanoma and benign nevi
title Protein expression of prognostic genes in primary melanoma and benign nevi
title_full Protein expression of prognostic genes in primary melanoma and benign nevi
title_fullStr Protein expression of prognostic genes in primary melanoma and benign nevi
title_full_unstemmed Protein expression of prognostic genes in primary melanoma and benign nevi
title_short Protein expression of prognostic genes in primary melanoma and benign nevi
title_sort protein expression of prognostic genes in primary melanoma and benign nevi
topic Original Article – Clinical Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9470607/
https://www.ncbi.nlm.nih.gov/pubmed/34757537
http://dx.doi.org/10.1007/s00432-021-03779-0
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