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Aminolevulinic Acid (ALA) as a Prodrug in Photodynamic Therapy of Cancer

Aminolevulinic acid (ALA) is an endogenous metabolite normally formed in the mitochondria from succinyl-CoA and glycine. Conjugation of eight ALA molecules yields protoporphyrin IX (PpIX) and finally leads to formation of heme. Conversion of PpIX to its downstream substrates requires the activity of...

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Autores principales: Wachowska, Małgorzata, Muchowicz, Angelika, Firczuk, Małgorzata, Gabrysiak, Magdalena, Winiarska, Magdalena, Wańczyk, Małgorzata, Bojarczuk, Kamil, Golab, Jakub
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263343/
http://dx.doi.org/10.3390/molecules16054140
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author Wachowska, Małgorzata
Muchowicz, Angelika
Firczuk, Małgorzata
Gabrysiak, Magdalena
Winiarska, Magdalena
Wańczyk, Małgorzata
Bojarczuk, Kamil
Golab, Jakub
author_facet Wachowska, Małgorzata
Muchowicz, Angelika
Firczuk, Małgorzata
Gabrysiak, Magdalena
Winiarska, Magdalena
Wańczyk, Małgorzata
Bojarczuk, Kamil
Golab, Jakub
author_sort Wachowska, Małgorzata
collection PubMed
description Aminolevulinic acid (ALA) is an endogenous metabolite normally formed in the mitochondria from succinyl-CoA and glycine. Conjugation of eight ALA molecules yields protoporphyrin IX (PpIX) and finally leads to formation of heme. Conversion of PpIX to its downstream substrates requires the activity of a rate-limiting enzyme ferrochelatase. When ALA is administered externally the abundantly produced PpIX cannot be quickly converted to its final product - heme by ferrochelatase and therefore accumulates within cells. Since PpIX is a potent photosensitizer this metabolic pathway can be exploited in photodynamic therapy (PDT). This is an already approved therapeutic strategy making ALA one of the most successful prodrugs used in cancer treatment.
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spelling pubmed-62633432018-12-10 Aminolevulinic Acid (ALA) as a Prodrug in Photodynamic Therapy of Cancer Wachowska, Małgorzata Muchowicz, Angelika Firczuk, Małgorzata Gabrysiak, Magdalena Winiarska, Magdalena Wańczyk, Małgorzata Bojarczuk, Kamil Golab, Jakub Molecules Review Aminolevulinic acid (ALA) is an endogenous metabolite normally formed in the mitochondria from succinyl-CoA and glycine. Conjugation of eight ALA molecules yields protoporphyrin IX (PpIX) and finally leads to formation of heme. Conversion of PpIX to its downstream substrates requires the activity of a rate-limiting enzyme ferrochelatase. When ALA is administered externally the abundantly produced PpIX cannot be quickly converted to its final product - heme by ferrochelatase and therefore accumulates within cells. Since PpIX is a potent photosensitizer this metabolic pathway can be exploited in photodynamic therapy (PDT). This is an already approved therapeutic strategy making ALA one of the most successful prodrugs used in cancer treatment. MDPI 2011-05-19 /pmc/articles/PMC6263343/ http://dx.doi.org/10.3390/molecules16054140 Text en © 2011 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/3.0/).
spellingShingle Review
Wachowska, Małgorzata
Muchowicz, Angelika
Firczuk, Małgorzata
Gabrysiak, Magdalena
Winiarska, Magdalena
Wańczyk, Małgorzata
Bojarczuk, Kamil
Golab, Jakub
Aminolevulinic Acid (ALA) as a Prodrug in Photodynamic Therapy of Cancer
title Aminolevulinic Acid (ALA) as a Prodrug in Photodynamic Therapy of Cancer
title_full Aminolevulinic Acid (ALA) as a Prodrug in Photodynamic Therapy of Cancer
title_fullStr Aminolevulinic Acid (ALA) as a Prodrug in Photodynamic Therapy of Cancer
title_full_unstemmed Aminolevulinic Acid (ALA) as a Prodrug in Photodynamic Therapy of Cancer
title_short Aminolevulinic Acid (ALA) as a Prodrug in Photodynamic Therapy of Cancer
title_sort aminolevulinic acid (ala) as a prodrug in photodynamic therapy of cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263343/
http://dx.doi.org/10.3390/molecules16054140
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