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A potentiated cooperation of carbonic anhydrase IX and histone deacetylase inhibitors against cancer
The emergence of tumour recurrence and resistance limits the survival rate for most tumour-bearing patients. Only, combination therapies targeting pathways involved in the induction and in the maintenance of cancer growth and progression might potentially result in an enhanced therapeutic efficacy....
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6968260/ https://www.ncbi.nlm.nih.gov/pubmed/31865754 http://dx.doi.org/10.1080/14756366.2019.1706090 |
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author | Ruzzolini, Jessica Laurenzana, Anna Andreucci, Elena Peppicelli, Silvia Bianchini, Francesca Carta, Fabrizio Supuran, Claudiu T. Romanelli, Maria Novella Nediani, Chiara Calorini, Lido |
author_facet | Ruzzolini, Jessica Laurenzana, Anna Andreucci, Elena Peppicelli, Silvia Bianchini, Francesca Carta, Fabrizio Supuran, Claudiu T. Romanelli, Maria Novella Nediani, Chiara Calorini, Lido |
author_sort | Ruzzolini, Jessica |
collection | PubMed |
description | The emergence of tumour recurrence and resistance limits the survival rate for most tumour-bearing patients. Only, combination therapies targeting pathways involved in the induction and in the maintenance of cancer growth and progression might potentially result in an enhanced therapeutic efficacy. Herein, we provided a prospective combination treatment that includes suberoylanilide hydroxamic acid (SAHA), a well-known inhibitor of histone deacetylases (HDACs), and SLC-0111, a novel inhibitor of carbonic anhydrase (CA) IX. We proved that HDAC inhibition with SAHA in combination with SLC-0111 affects cell viability and colony forming capability to greater extent than either treatment alone of breast, colorectal and melanoma cancer cells. At the molecular level, this therapeutic regimen resulted in a synergistically increase of histone H4 and p53 acetylation in all tested cell lines. Overall, our findings showed that SAHA and SLC-0111 can be regarded as very attractive combination providing a potential therapeutic strategy against different cancer models. |
format | Online Article Text |
id | pubmed-6968260 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-69682602020-01-30 A potentiated cooperation of carbonic anhydrase IX and histone deacetylase inhibitors against cancer Ruzzolini, Jessica Laurenzana, Anna Andreucci, Elena Peppicelli, Silvia Bianchini, Francesca Carta, Fabrizio Supuran, Claudiu T. Romanelli, Maria Novella Nediani, Chiara Calorini, Lido J Enzyme Inhib Med Chem Research Paper The emergence of tumour recurrence and resistance limits the survival rate for most tumour-bearing patients. Only, combination therapies targeting pathways involved in the induction and in the maintenance of cancer growth and progression might potentially result in an enhanced therapeutic efficacy. Herein, we provided a prospective combination treatment that includes suberoylanilide hydroxamic acid (SAHA), a well-known inhibitor of histone deacetylases (HDACs), and SLC-0111, a novel inhibitor of carbonic anhydrase (CA) IX. We proved that HDAC inhibition with SAHA in combination with SLC-0111 affects cell viability and colony forming capability to greater extent than either treatment alone of breast, colorectal and melanoma cancer cells. At the molecular level, this therapeutic regimen resulted in a synergistically increase of histone H4 and p53 acetylation in all tested cell lines. Overall, our findings showed that SAHA and SLC-0111 can be regarded as very attractive combination providing a potential therapeutic strategy against different cancer models. Taylor & Francis 2019-12-22 /pmc/articles/PMC6968260/ /pubmed/31865754 http://dx.doi.org/10.1080/14756366.2019.1706090 Text en © 2019 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 Ruzzolini, Jessica Laurenzana, Anna Andreucci, Elena Peppicelli, Silvia Bianchini, Francesca Carta, Fabrizio Supuran, Claudiu T. Romanelli, Maria Novella Nediani, Chiara Calorini, Lido A potentiated cooperation of carbonic anhydrase IX and histone deacetylase inhibitors against cancer |
title | A potentiated cooperation of carbonic anhydrase IX and histone deacetylase inhibitors against cancer |
title_full | A potentiated cooperation of carbonic anhydrase IX and histone deacetylase inhibitors against cancer |
title_fullStr | A potentiated cooperation of carbonic anhydrase IX and histone deacetylase inhibitors against cancer |
title_full_unstemmed | A potentiated cooperation of carbonic anhydrase IX and histone deacetylase inhibitors against cancer |
title_short | A potentiated cooperation of carbonic anhydrase IX and histone deacetylase inhibitors against cancer |
title_sort | potentiated cooperation of carbonic anhydrase ix and histone deacetylase inhibitors against cancer |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6968260/ https://www.ncbi.nlm.nih.gov/pubmed/31865754 http://dx.doi.org/10.1080/14756366.2019.1706090 |
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