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Cell Death Inducing Microbial Protein Phosphatase Inhibitors—Mechanisms of Action

Okadaic acid (OA) and microcystin (MC) as well as several other microbial toxins like nodularin and calyculinA are known as tumor promoters as well as inducers of apoptotic cell death. Their intracellular targets are the major serine/threonine protein phosphatases. This review summarizes mechanisms...

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Autores principales: Kleppe, Rune, Herfindal, Lars, Døskeland, Stein Ove
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4626703/
https://www.ncbi.nlm.nih.gov/pubmed/26506362
http://dx.doi.org/10.3390/md13106505
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author Kleppe, Rune
Herfindal, Lars
Døskeland, Stein Ove
author_facet Kleppe, Rune
Herfindal, Lars
Døskeland, Stein Ove
author_sort Kleppe, Rune
collection PubMed
description Okadaic acid (OA) and microcystin (MC) as well as several other microbial toxins like nodularin and calyculinA are known as tumor promoters as well as inducers of apoptotic cell death. Their intracellular targets are the major serine/threonine protein phosphatases. This review summarizes mechanisms believed to be responsible for the death induction and tumor promotion with focus on the interdependent production of reactive oxygen species (ROS) and activation of Ca(2+)/calmodulin kinase II (CaM-KII). New data are presented using inhibitors of specific ROS producing enzymes to curb nodularin/MC-induced liver cell (hepatocyte) death. They indicate that enzymes of the arachidonic acid pathway, notably phospholipase A2, 5-lipoxygenase, and cyclooxygenases, may be required for nodularin/MC-induced (and presumably OA-induced) cell death, suggesting new ways to overcome at least some aspects of OA and MC toxicity.
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spelling pubmed-46267032015-11-12 Cell Death Inducing Microbial Protein Phosphatase Inhibitors—Mechanisms of Action Kleppe, Rune Herfindal, Lars Døskeland, Stein Ove Mar Drugs Review Okadaic acid (OA) and microcystin (MC) as well as several other microbial toxins like nodularin and calyculinA are known as tumor promoters as well as inducers of apoptotic cell death. Their intracellular targets are the major serine/threonine protein phosphatases. This review summarizes mechanisms believed to be responsible for the death induction and tumor promotion with focus on the interdependent production of reactive oxygen species (ROS) and activation of Ca(2+)/calmodulin kinase II (CaM-KII). New data are presented using inhibitors of specific ROS producing enzymes to curb nodularin/MC-induced liver cell (hepatocyte) death. They indicate that enzymes of the arachidonic acid pathway, notably phospholipase A2, 5-lipoxygenase, and cyclooxygenases, may be required for nodularin/MC-induced (and presumably OA-induced) cell death, suggesting new ways to overcome at least some aspects of OA and MC toxicity. MDPI 2015-10-22 /pmc/articles/PMC4626703/ /pubmed/26506362 http://dx.doi.org/10.3390/md13106505 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
Kleppe, Rune
Herfindal, Lars
Døskeland, Stein Ove
Cell Death Inducing Microbial Protein Phosphatase Inhibitors—Mechanisms of Action
title Cell Death Inducing Microbial Protein Phosphatase Inhibitors—Mechanisms of Action
title_full Cell Death Inducing Microbial Protein Phosphatase Inhibitors—Mechanisms of Action
title_fullStr Cell Death Inducing Microbial Protein Phosphatase Inhibitors—Mechanisms of Action
title_full_unstemmed Cell Death Inducing Microbial Protein Phosphatase Inhibitors—Mechanisms of Action
title_short Cell Death Inducing Microbial Protein Phosphatase Inhibitors—Mechanisms of Action
title_sort cell death inducing microbial protein phosphatase inhibitors—mechanisms of action
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4626703/
https://www.ncbi.nlm.nih.gov/pubmed/26506362
http://dx.doi.org/10.3390/md13106505
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