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Discovery of a new molecule inducing melanoma cell death: dual AMPK/MELK targeting for novel melanoma therapies
In the search of biguanide-derived molecules against melanoma, we have discovered and developed a series of bioactive products and identified the promising new compound CRO15. This molecule exerted anti-melanoma effects on cells lines and cells isolated from patients including the ones derived from...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7801734/ https://www.ncbi.nlm.nih.gov/pubmed/33431809 http://dx.doi.org/10.1038/s41419-020-03344-6 |
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author | Jaune, Emilie Cavazza, Elisa Ronco, Cyril Grytsai, Oleksandr Abbe, Patricia Tekaya, Nedra Zerhouni, Marwa Beranger, Guillaume Kaminski, Lisa Bost, Frédéric Gesson, Maeva Tulic, Meri Hofman, Paul Ballotti, Robert Passeron, Thierry Botton, Thomas Benhida, Rachid Rocchi, Stéphane |
author_facet | Jaune, Emilie Cavazza, Elisa Ronco, Cyril Grytsai, Oleksandr Abbe, Patricia Tekaya, Nedra Zerhouni, Marwa Beranger, Guillaume Kaminski, Lisa Bost, Frédéric Gesson, Maeva Tulic, Meri Hofman, Paul Ballotti, Robert Passeron, Thierry Botton, Thomas Benhida, Rachid Rocchi, Stéphane |
author_sort | Jaune, Emilie |
collection | PubMed |
description | In the search of biguanide-derived molecules against melanoma, we have discovered and developed a series of bioactive products and identified the promising new compound CRO15. This molecule exerted anti-melanoma effects on cells lines and cells isolated from patients including the ones derived from tumors resistant to BRAF inhibitors. Moreover, CRO15 was able to decrease viability of cells lines from a broad range of cancer types. This compound acts by two distinct mechanisms. First by activating the AMPK pathway induced by a mitochondrial disorder. Second by inhibition of MELK kinase activity, which induces cell cycle arrest and activation of DNA damage repair pathways by p53 and REDD1 activation. All of these mechanisms activate autophagic and apoptotic processes resulting in melanoma cell death. The strong efficacy of CRO15 to reduce the growth of melanoma xenograft sensitive or resistant to BRAF inhibitors opens interesting perspective. |
format | Online Article Text |
id | pubmed-7801734 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78017342021-01-21 Discovery of a new molecule inducing melanoma cell death: dual AMPK/MELK targeting for novel melanoma therapies Jaune, Emilie Cavazza, Elisa Ronco, Cyril Grytsai, Oleksandr Abbe, Patricia Tekaya, Nedra Zerhouni, Marwa Beranger, Guillaume Kaminski, Lisa Bost, Frédéric Gesson, Maeva Tulic, Meri Hofman, Paul Ballotti, Robert Passeron, Thierry Botton, Thomas Benhida, Rachid Rocchi, Stéphane Cell Death Dis Article In the search of biguanide-derived molecules against melanoma, we have discovered and developed a series of bioactive products and identified the promising new compound CRO15. This molecule exerted anti-melanoma effects on cells lines and cells isolated from patients including the ones derived from tumors resistant to BRAF inhibitors. Moreover, CRO15 was able to decrease viability of cells lines from a broad range of cancer types. This compound acts by two distinct mechanisms. First by activating the AMPK pathway induced by a mitochondrial disorder. Second by inhibition of MELK kinase activity, which induces cell cycle arrest and activation of DNA damage repair pathways by p53 and REDD1 activation. All of these mechanisms activate autophagic and apoptotic processes resulting in melanoma cell death. The strong efficacy of CRO15 to reduce the growth of melanoma xenograft sensitive or resistant to BRAF inhibitors opens interesting perspective. Nature Publishing Group UK 2021-01-11 /pmc/articles/PMC7801734/ /pubmed/33431809 http://dx.doi.org/10.1038/s41419-020-03344-6 Text en © The Author(s) 2021 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 Jaune, Emilie Cavazza, Elisa Ronco, Cyril Grytsai, Oleksandr Abbe, Patricia Tekaya, Nedra Zerhouni, Marwa Beranger, Guillaume Kaminski, Lisa Bost, Frédéric Gesson, Maeva Tulic, Meri Hofman, Paul Ballotti, Robert Passeron, Thierry Botton, Thomas Benhida, Rachid Rocchi, Stéphane Discovery of a new molecule inducing melanoma cell death: dual AMPK/MELK targeting for novel melanoma therapies |
title | Discovery of a new molecule inducing melanoma cell death: dual AMPK/MELK targeting for novel melanoma therapies |
title_full | Discovery of a new molecule inducing melanoma cell death: dual AMPK/MELK targeting for novel melanoma therapies |
title_fullStr | Discovery of a new molecule inducing melanoma cell death: dual AMPK/MELK targeting for novel melanoma therapies |
title_full_unstemmed | Discovery of a new molecule inducing melanoma cell death: dual AMPK/MELK targeting for novel melanoma therapies |
title_short | Discovery of a new molecule inducing melanoma cell death: dual AMPK/MELK targeting for novel melanoma therapies |
title_sort | discovery of a new molecule inducing melanoma cell death: dual ampk/melk targeting for novel melanoma therapies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7801734/ https://www.ncbi.nlm.nih.gov/pubmed/33431809 http://dx.doi.org/10.1038/s41419-020-03344-6 |
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