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A comparative study of carbonic anhydrase activity in lymphocytes from colorectal cancer tissues and adjacent healthy counterparts
Several carbonic anhydrase (CA, EC 4.2.1.1) isoforms play an essential role in processes connected to tumorigenesis, as they efficiently accelerate the hydration of carbon dioxide to bicarbonate and proton. In this context, examples are CA IX and CA XII, which were proved to be upregulated in many s...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9225793/ https://www.ncbi.nlm.nih.gov/pubmed/35695123 http://dx.doi.org/10.1080/14756366.2022.2085694 |
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author | Nannini, Giulia De Luca, Viviana D’Ambrosio, Chiara Scaloni, Andrea Taddei, Antonio Ringressi, Maria Novella Cianchi, Fabio Staderini, Fabio Capasso, Clemente Amedei, Amedeo Supuran, Claudiu T. |
author_facet | Nannini, Giulia De Luca, Viviana D’Ambrosio, Chiara Scaloni, Andrea Taddei, Antonio Ringressi, Maria Novella Cianchi, Fabio Staderini, Fabio Capasso, Clemente Amedei, Amedeo Supuran, Claudiu T. |
author_sort | Nannini, Giulia |
collection | PubMed |
description | Several carbonic anhydrase (CA, EC 4.2.1.1) isoforms play an essential role in processes connected to tumorigenesis, as they efficiently accelerate the hydration of carbon dioxide to bicarbonate and proton. In this context, examples are CA IX and CA XII, which were proved to be upregulated in many solid malignancies. On the other hand, cancer and the immune system are inextricably linked, and targeting the immune checkpoints recently was shown to efficiently improve the treatment of malignancies. In this study, we have investigated the expression of CA isoforms in tumour-infiltrating lymphocytes (TILs) that, according to the immunosurveillance theory, were suggested to have a crucial role in the development of colorectal cancer (CRC). T lymphocytes isolated from healthy surrounding mucosa showed a higher CA activity compared to those present in tumour and peripheral blood in the same patients. CA I and II were confirmed as enzyme isoforms involved in the process, as determined by proteomic analysis of corresponding TIL samples. These preliminary findings suggest a dysregulation of the local immune response in the CRC tissues and a loss of effective anticancer mechanisms mediated by CAs therein. |
format | Online Article Text |
id | pubmed-9225793 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-92257932022-06-24 A comparative study of carbonic anhydrase activity in lymphocytes from colorectal cancer tissues and adjacent healthy counterparts Nannini, Giulia De Luca, Viviana D’Ambrosio, Chiara Scaloni, Andrea Taddei, Antonio Ringressi, Maria Novella Cianchi, Fabio Staderini, Fabio Capasso, Clemente Amedei, Amedeo Supuran, Claudiu T. J Enzyme Inhib Med Chem Research Paper Several carbonic anhydrase (CA, EC 4.2.1.1) isoforms play an essential role in processes connected to tumorigenesis, as they efficiently accelerate the hydration of carbon dioxide to bicarbonate and proton. In this context, examples are CA IX and CA XII, which were proved to be upregulated in many solid malignancies. On the other hand, cancer and the immune system are inextricably linked, and targeting the immune checkpoints recently was shown to efficiently improve the treatment of malignancies. In this study, we have investigated the expression of CA isoforms in tumour-infiltrating lymphocytes (TILs) that, according to the immunosurveillance theory, were suggested to have a crucial role in the development of colorectal cancer (CRC). T lymphocytes isolated from healthy surrounding mucosa showed a higher CA activity compared to those present in tumour and peripheral blood in the same patients. CA I and II were confirmed as enzyme isoforms involved in the process, as determined by proteomic analysis of corresponding TIL samples. These preliminary findings suggest a dysregulation of the local immune response in the CRC tissues and a loss of effective anticancer mechanisms mediated by CAs therein. Taylor & Francis 2022-06-13 /pmc/articles/PMC9225793/ /pubmed/35695123 http://dx.doi.org/10.1080/14756366.2022.2085694 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paper Nannini, Giulia De Luca, Viviana D’Ambrosio, Chiara Scaloni, Andrea Taddei, Antonio Ringressi, Maria Novella Cianchi, Fabio Staderini, Fabio Capasso, Clemente Amedei, Amedeo Supuran, Claudiu T. A comparative study of carbonic anhydrase activity in lymphocytes from colorectal cancer tissues and adjacent healthy counterparts |
title | A comparative study of carbonic anhydrase activity in lymphocytes from colorectal cancer tissues and adjacent healthy counterparts |
title_full | A comparative study of carbonic anhydrase activity in lymphocytes from colorectal cancer tissues and adjacent healthy counterparts |
title_fullStr | A comparative study of carbonic anhydrase activity in lymphocytes from colorectal cancer tissues and adjacent healthy counterparts |
title_full_unstemmed | A comparative study of carbonic anhydrase activity in lymphocytes from colorectal cancer tissues and adjacent healthy counterparts |
title_short | A comparative study of carbonic anhydrase activity in lymphocytes from colorectal cancer tissues and adjacent healthy counterparts |
title_sort | comparative study of carbonic anhydrase activity in lymphocytes from colorectal cancer tissues and adjacent healthy counterparts |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9225793/ https://www.ncbi.nlm.nih.gov/pubmed/35695123 http://dx.doi.org/10.1080/14756366.2022.2085694 |
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