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Complete Acid Ceramidase ablation prevents cancer-initiating cell formation in melanoma cells
Acid ceramidase (AC) is a lysosomal cysteine hydrolase that catalyzes the conversion of ceramide into fatty acid and sphingosine. This reaction lowers intracellular ceramide levels and concomitantly generates sphingosine used for sphingosine-1-phosphate (S1P) production. Since increases in ceramide...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5547127/ https://www.ncbi.nlm.nih.gov/pubmed/28785021 http://dx.doi.org/10.1038/s41598-017-07606-w |
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author | Lai, Michele Realini, Natalia La Ferla, Marco Passalacqua, Ilaria Matteoli, Giulia Ganesan, Anand Pistello, Mauro Mazzanti, Chiara Maria Piomelli, Daniele |
author_facet | Lai, Michele Realini, Natalia La Ferla, Marco Passalacqua, Ilaria Matteoli, Giulia Ganesan, Anand Pistello, Mauro Mazzanti, Chiara Maria Piomelli, Daniele |
author_sort | Lai, Michele |
collection | PubMed |
description | Acid ceramidase (AC) is a lysosomal cysteine hydrolase that catalyzes the conversion of ceramide into fatty acid and sphingosine. This reaction lowers intracellular ceramide levels and concomitantly generates sphingosine used for sphingosine-1-phosphate (S1P) production. Since increases in ceramide and consequent decreases of S1P reduce proliferation of various cancers, AC might offer a new target for anti-tumor therapy. Here we used CrispR-Cas9-mediated gene editing to delete the gene encoding for AC, ASAH1, in human A375 melanoma cells. ASAH1-null clones show significantly greater accumulation of long-chain saturated ceramides that are substrate for AC. As seen with administration of exogenous ceramide, AC ablation blocks cell cycle progression and accelerates senescence. Importantly, ASAH1-null cells also lose the ability to form cancer-initiating cells and to undergo self-renewal, which is suggestive of a key role for AC in maintaining malignancy and self-renewal of invasive melanoma cells. The results suggest that AC inhibitors might find therapeutic use as adjuvant therapy for advanced melanoma. |
format | Online Article Text |
id | pubmed-5547127 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55471272017-08-09 Complete Acid Ceramidase ablation prevents cancer-initiating cell formation in melanoma cells Lai, Michele Realini, Natalia La Ferla, Marco Passalacqua, Ilaria Matteoli, Giulia Ganesan, Anand Pistello, Mauro Mazzanti, Chiara Maria Piomelli, Daniele Sci Rep Article Acid ceramidase (AC) is a lysosomal cysteine hydrolase that catalyzes the conversion of ceramide into fatty acid and sphingosine. This reaction lowers intracellular ceramide levels and concomitantly generates sphingosine used for sphingosine-1-phosphate (S1P) production. Since increases in ceramide and consequent decreases of S1P reduce proliferation of various cancers, AC might offer a new target for anti-tumor therapy. Here we used CrispR-Cas9-mediated gene editing to delete the gene encoding for AC, ASAH1, in human A375 melanoma cells. ASAH1-null clones show significantly greater accumulation of long-chain saturated ceramides that are substrate for AC. As seen with administration of exogenous ceramide, AC ablation blocks cell cycle progression and accelerates senescence. Importantly, ASAH1-null cells also lose the ability to form cancer-initiating cells and to undergo self-renewal, which is suggestive of a key role for AC in maintaining malignancy and self-renewal of invasive melanoma cells. The results suggest that AC inhibitors might find therapeutic use as adjuvant therapy for advanced melanoma. Nature Publishing Group UK 2017-08-07 /pmc/articles/PMC5547127/ /pubmed/28785021 http://dx.doi.org/10.1038/s41598-017-07606-w Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Lai, Michele Realini, Natalia La Ferla, Marco Passalacqua, Ilaria Matteoli, Giulia Ganesan, Anand Pistello, Mauro Mazzanti, Chiara Maria Piomelli, Daniele Complete Acid Ceramidase ablation prevents cancer-initiating cell formation in melanoma cells |
title | Complete Acid Ceramidase ablation prevents cancer-initiating cell formation in melanoma cells |
title_full | Complete Acid Ceramidase ablation prevents cancer-initiating cell formation in melanoma cells |
title_fullStr | Complete Acid Ceramidase ablation prevents cancer-initiating cell formation in melanoma cells |
title_full_unstemmed | Complete Acid Ceramidase ablation prevents cancer-initiating cell formation in melanoma cells |
title_short | Complete Acid Ceramidase ablation prevents cancer-initiating cell formation in melanoma cells |
title_sort | complete acid ceramidase ablation prevents cancer-initiating cell formation in melanoma cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5547127/ https://www.ncbi.nlm.nih.gov/pubmed/28785021 http://dx.doi.org/10.1038/s41598-017-07606-w |
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