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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2022
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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.
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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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