Carbonic Anhydrase Inhibition and the Management of Hypoxic Tumors

Hypoxia and acidosis are salient features of many tumors, leading to a completely different metabolism compared to normal cells. Two of the simplest metabolic products, protons and bicarbonate, are generated by the catalytic activity of the metalloenzyme carbonic anhydrase (CA, EC 4.2.1.1), with at...

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Main Author: Claudiu T. Supuran
Format: Article
Language:English
Published: MDPI AG 2017-09-01
Series:Metabolites
Subjects:
Online Access:https://www.mdpi.com/2218-1989/7/3/48
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spelling doaj-3e1e3c527442491f9a8f2d8857f11cd62020-11-25T00:52:59ZengMDPI AGMetabolites2218-19892017-09-01734810.3390/metabo7030048metabo7030048Carbonic Anhydrase Inhibition and the Management of Hypoxic TumorsClaudiu T. Supuran0Università degli Studi di Firenze, Dipartimento Neurofarba, Sezione di Scienze Farmaceutiche e Nutraceutiche, Via U. Schiff 6, 50019 Sesto Fiorentino, Florence, ItalyHypoxia and acidosis are salient features of many tumors, leading to a completely different metabolism compared to normal cells. Two of the simplest metabolic products, protons and bicarbonate, are generated by the catalytic activity of the metalloenzyme carbonic anhydrase (CA, EC 4.2.1.1), with at least two of its isoforms, CA IX and XII, mainly present in hypoxic tumors. Inhibition of tumor-associated CAs leads to an impaired growth of the primary tumors, metastases and reduces the population of cancer stem cells, leading thus to a complex and beneficial anticancer action for this class of enzyme inhibitors. In this review, I will present the state of the art on the development of CA inhibitors (CAIs) targeting the tumor-associated CA isoforms, which may have applications for the treatment and imaging of cancers expressing them. Small molecule inhibitors, one of which (SLC-0111) completed Phase I clinical trials, and antibodies (girentuximab, discontinued in Phase III clinical trials) will be discussed, together with the various approaches used to design anticancer agents with a new mechanism of action based on interference with these crucial metabolites, protons and bicarbonate.https://www.mdpi.com/2218-1989/7/3/48tumormetabolismcarbonic anhydraseisoforms IX and XIIinhibitorsulfonamideantibody
collection DOAJ
language English
format Article
sources DOAJ
author Claudiu T. Supuran
spellingShingle Claudiu T. Supuran
Carbonic Anhydrase Inhibition and the Management of Hypoxic Tumors
Metabolites
tumor
metabolism
carbonic anhydrase
isoforms IX and XII
inhibitor
sulfonamide
antibody
author_facet Claudiu T. Supuran
author_sort Claudiu T. Supuran
title Carbonic Anhydrase Inhibition and the Management of Hypoxic Tumors
title_short Carbonic Anhydrase Inhibition and the Management of Hypoxic Tumors
title_full Carbonic Anhydrase Inhibition and the Management of Hypoxic Tumors
title_fullStr Carbonic Anhydrase Inhibition and the Management of Hypoxic Tumors
title_full_unstemmed Carbonic Anhydrase Inhibition and the Management of Hypoxic Tumors
title_sort carbonic anhydrase inhibition and the management of hypoxic tumors
publisher MDPI AG
series Metabolites
issn 2218-1989
publishDate 2017-09-01
description Hypoxia and acidosis are salient features of many tumors, leading to a completely different metabolism compared to normal cells. Two of the simplest metabolic products, protons and bicarbonate, are generated by the catalytic activity of the metalloenzyme carbonic anhydrase (CA, EC 4.2.1.1), with at least two of its isoforms, CA IX and XII, mainly present in hypoxic tumors. Inhibition of tumor-associated CAs leads to an impaired growth of the primary tumors, metastases and reduces the population of cancer stem cells, leading thus to a complex and beneficial anticancer action for this class of enzyme inhibitors. In this review, I will present the state of the art on the development of CA inhibitors (CAIs) targeting the tumor-associated CA isoforms, which may have applications for the treatment and imaging of cancers expressing them. Small molecule inhibitors, one of which (SLC-0111) completed Phase I clinical trials, and antibodies (girentuximab, discontinued in Phase III clinical trials) will be discussed, together with the various approaches used to design anticancer agents with a new mechanism of action based on interference with these crucial metabolites, protons and bicarbonate.
topic tumor
metabolism
carbonic anhydrase
isoforms IX and XII
inhibitor
sulfonamide
antibody
url https://www.mdpi.com/2218-1989/7/3/48
work_keys_str_mv AT claudiutsupuran carbonicanhydraseinhibitionandthemanagementofhypoxictumors
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