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Targeting Carbonic Anhydrase IX Activity and Expression

Metastatic tumors are often hypoxic exhibiting a decrease in extracellular pH (~6.5) due to a metabolic transition described by the Warburg Effect. This shift in tumor cell metabolism alters the tumor milieu inducing tumor cell proliferation, angiogenesis, cell motility, invasiveness, and often resi...

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Autores principales: Mahon, Brian P., Pinard, Melissa A., McKenna, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272707/
https://www.ncbi.nlm.nih.gov/pubmed/25647573
http://dx.doi.org/10.3390/molecules20022323
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author Mahon, Brian P.
Pinard, Melissa A.
McKenna, Robert
author_facet Mahon, Brian P.
Pinard, Melissa A.
McKenna, Robert
author_sort Mahon, Brian P.
collection PubMed
description Metastatic tumors are often hypoxic exhibiting a decrease in extracellular pH (~6.5) due to a metabolic transition described by the Warburg Effect. This shift in tumor cell metabolism alters the tumor milieu inducing tumor cell proliferation, angiogenesis, cell motility, invasiveness, and often resistance to common anti-cancer treatments; hence hindering treatment of aggressive cancers. As a result, tumors exhibiting this phenotype are directly associated with poor prognosis and decreased survival rates in cancer patients. A key component to this tumor microenvironment is carbonic anhydrase IX (CA IX). Knockdown of CA IX expression or inhibition of its activity has been shown to reduce primary tumor growth, tumor proliferation, and also decrease tumor resistance to conventional anti-cancer therapies. As such several approaches have been taken to target CA IX in tumors via small-molecule, anti-body, and RNAi delivery systems. Here we will review recent developments that have exploited these approaches and provide our thoughts for future directions of CA IX targeting for the treatment of cancer.
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spelling pubmed-62727072018-12-13 Targeting Carbonic Anhydrase IX Activity and Expression Mahon, Brian P. Pinard, Melissa A. McKenna, Robert Molecules Review Metastatic tumors are often hypoxic exhibiting a decrease in extracellular pH (~6.5) due to a metabolic transition described by the Warburg Effect. This shift in tumor cell metabolism alters the tumor milieu inducing tumor cell proliferation, angiogenesis, cell motility, invasiveness, and often resistance to common anti-cancer treatments; hence hindering treatment of aggressive cancers. As a result, tumors exhibiting this phenotype are directly associated with poor prognosis and decreased survival rates in cancer patients. A key component to this tumor microenvironment is carbonic anhydrase IX (CA IX). Knockdown of CA IX expression or inhibition of its activity has been shown to reduce primary tumor growth, tumor proliferation, and also decrease tumor resistance to conventional anti-cancer therapies. As such several approaches have been taken to target CA IX in tumors via small-molecule, anti-body, and RNAi delivery systems. Here we will review recent developments that have exploited these approaches and provide our thoughts for future directions of CA IX targeting for the treatment of cancer. MDPI 2015-01-30 /pmc/articles/PMC6272707/ /pubmed/25647573 http://dx.doi.org/10.3390/molecules20022323 Text en © 2015 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Mahon, Brian P.
Pinard, Melissa A.
McKenna, Robert
Targeting Carbonic Anhydrase IX Activity and Expression
title Targeting Carbonic Anhydrase IX Activity and Expression
title_full Targeting Carbonic Anhydrase IX Activity and Expression
title_fullStr Targeting Carbonic Anhydrase IX Activity and Expression
title_full_unstemmed Targeting Carbonic Anhydrase IX Activity and Expression
title_short Targeting Carbonic Anhydrase IX Activity and Expression
title_sort targeting carbonic anhydrase ix activity and expression
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272707/
https://www.ncbi.nlm.nih.gov/pubmed/25647573
http://dx.doi.org/10.3390/molecules20022323
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