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Immunohistochemical analysis of Tn antigen expression in colorectal adenocarcinoma and precursor lesions

BACKGROUND: The Tn antigen (CD175) is an O-glycan expressed in various types of human adenocarcinomas, including colorectal cancer (CRC), though prior studies have relied heavily upon poorly characterized in-house generated antibodies and lectins. In this study, we explored Tn expression in CRC usin...

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Autores principales: Dombek, Gabrielle E., Ore, Ana Sofia, Cheng, Jane, Matsumoto, Yasuyuki, Glickman, Jonathan N., Fleishman, Aaron, Heimburg-Molinaro, Jamie, Poylin, Vitaliy Y., Fabrizio, Anne, Cataldo, Thomas, Messaris, Evangelos, Cummings, Richard D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9730631/
https://www.ncbi.nlm.nih.gov/pubmed/36476111
http://dx.doi.org/10.1186/s12885-022-10376-y
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author Dombek, Gabrielle E.
Ore, Ana Sofia
Cheng, Jane
Matsumoto, Yasuyuki
Glickman, Jonathan N.
Fleishman, Aaron
Heimburg-Molinaro, Jamie
Poylin, Vitaliy Y.
Fabrizio, Anne
Cataldo, Thomas
Messaris, Evangelos
Cummings, Richard D.
author_facet Dombek, Gabrielle E.
Ore, Ana Sofia
Cheng, Jane
Matsumoto, Yasuyuki
Glickman, Jonathan N.
Fleishman, Aaron
Heimburg-Molinaro, Jamie
Poylin, Vitaliy Y.
Fabrizio, Anne
Cataldo, Thomas
Messaris, Evangelos
Cummings, Richard D.
author_sort Dombek, Gabrielle E.
collection PubMed
description BACKGROUND: The Tn antigen (CD175) is an O-glycan expressed in various types of human adenocarcinomas, including colorectal cancer (CRC), though prior studies have relied heavily upon poorly characterized in-house generated antibodies and lectins. In this study, we explored Tn expression in CRC using ReBaGs6, a well-characterized recombinant murine antibody with high specificity for clustered Tn antigen. METHODS: Using well-defined monoclonal antibodies, expression patterns of Tn and sialylated Tn (STn) antigens were characterized by immunostaining in CRC, in matched peritumoral [transitional margin (TM)] mucosa, and in normal colonic mucosa distant from the tumor, as well as in adenomas. Vicia villosa agglutinin lectin was used to detect terminal GalNAc expression. Histo-scoring (H scoring) of staining was carried out, and pairwise comparisons of staining levels between tissue types were performed using paired samples Wilcoxon rank sum tests, with statistical significance set at 0.05. RESULTS: While minimal intracellular Tn staining was seen in normal mucosa, significantly higher expression was observed in both TM mucosa (p < 0.001) and adenocarcinoma (p < 0.001). This pattern was reflected to a lesser degree by STn expression in these tissue types. Interestingly, TM mucosa demonstrates a Tn expression level even higher than that of the adenocarcinoma itself (p = 0.019). Colorectal adenomas demonstrated greater Tn and STn expression relative to normal mucosa (p < 0.001 and p = 0.012, respectively). CONCLUSIONS: In summary, CRC is characterized by alterations in Tn/STn antigen expression in neoplastic epithelium as well as peritumoral benign mucosa. Tn/STn antigens are seldom expressed in normal mucosa. This suggests that TM mucosa, in addition to CRC itself, represents a source of glycoproteins rich in Tn that may offer future biomarker targets. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-022-10376-y.
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spelling pubmed-97306312022-12-09 Immunohistochemical analysis of Tn antigen expression in colorectal adenocarcinoma and precursor lesions Dombek, Gabrielle E. Ore, Ana Sofia Cheng, Jane Matsumoto, Yasuyuki Glickman, Jonathan N. Fleishman, Aaron Heimburg-Molinaro, Jamie Poylin, Vitaliy Y. Fabrizio, Anne Cataldo, Thomas Messaris, Evangelos Cummings, Richard D. BMC Cancer Research BACKGROUND: The Tn antigen (CD175) is an O-glycan expressed in various types of human adenocarcinomas, including colorectal cancer (CRC), though prior studies have relied heavily upon poorly characterized in-house generated antibodies and lectins. In this study, we explored Tn expression in CRC using ReBaGs6, a well-characterized recombinant murine antibody with high specificity for clustered Tn antigen. METHODS: Using well-defined monoclonal antibodies, expression patterns of Tn and sialylated Tn (STn) antigens were characterized by immunostaining in CRC, in matched peritumoral [transitional margin (TM)] mucosa, and in normal colonic mucosa distant from the tumor, as well as in adenomas. Vicia villosa agglutinin lectin was used to detect terminal GalNAc expression. Histo-scoring (H scoring) of staining was carried out, and pairwise comparisons of staining levels between tissue types were performed using paired samples Wilcoxon rank sum tests, with statistical significance set at 0.05. RESULTS: While minimal intracellular Tn staining was seen in normal mucosa, significantly higher expression was observed in both TM mucosa (p < 0.001) and adenocarcinoma (p < 0.001). This pattern was reflected to a lesser degree by STn expression in these tissue types. Interestingly, TM mucosa demonstrates a Tn expression level even higher than that of the adenocarcinoma itself (p = 0.019). Colorectal adenomas demonstrated greater Tn and STn expression relative to normal mucosa (p < 0.001 and p = 0.012, respectively). CONCLUSIONS: In summary, CRC is characterized by alterations in Tn/STn antigen expression in neoplastic epithelium as well as peritumoral benign mucosa. Tn/STn antigens are seldom expressed in normal mucosa. This suggests that TM mucosa, in addition to CRC itself, represents a source of glycoproteins rich in Tn that may offer future biomarker targets. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-022-10376-y. BioMed Central 2022-12-07 /pmc/articles/PMC9730631/ /pubmed/36476111 http://dx.doi.org/10.1186/s12885-022-10376-y Text en © The Author(s) 2022 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Dombek, Gabrielle E.
Ore, Ana Sofia
Cheng, Jane
Matsumoto, Yasuyuki
Glickman, Jonathan N.
Fleishman, Aaron
Heimburg-Molinaro, Jamie
Poylin, Vitaliy Y.
Fabrizio, Anne
Cataldo, Thomas
Messaris, Evangelos
Cummings, Richard D.
Immunohistochemical analysis of Tn antigen expression in colorectal adenocarcinoma and precursor lesions
title Immunohistochemical analysis of Tn antigen expression in colorectal adenocarcinoma and precursor lesions
title_full Immunohistochemical analysis of Tn antigen expression in colorectal adenocarcinoma and precursor lesions
title_fullStr Immunohistochemical analysis of Tn antigen expression in colorectal adenocarcinoma and precursor lesions
title_full_unstemmed Immunohistochemical analysis of Tn antigen expression in colorectal adenocarcinoma and precursor lesions
title_short Immunohistochemical analysis of Tn antigen expression in colorectal adenocarcinoma and precursor lesions
title_sort immunohistochemical analysis of tn antigen expression in colorectal adenocarcinoma and precursor lesions
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9730631/
https://www.ncbi.nlm.nih.gov/pubmed/36476111
http://dx.doi.org/10.1186/s12885-022-10376-y
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