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Antitumor activity and expression profiles of genes induced by sulforaphane in human melanoma cells
PURPOSE: Human melanoma is a highly aggressive incurable cancer due to intrinsic cellular resistance to apoptosis, reprogramming, proliferation and survival during tumour progression. Sulforaphane (SFN), an isothiocyanate found in cruciferous vegetables, plays a role in carcinogenesis in many cancer...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6182666/ https://www.ncbi.nlm.nih.gov/pubmed/28864908 http://dx.doi.org/10.1007/s00394-017-1527-7 |
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author | Arcidiacono, Paola Ragonese, Francesco Stabile, Anna Pistilli, Alessandra Kuligina, Ekaterina Rende, Mario Bottoni, Ugo Calvieri, Stefano Crisanti, Andrea Spaccapelo, Roberta |
author_facet | Arcidiacono, Paola Ragonese, Francesco Stabile, Anna Pistilli, Alessandra Kuligina, Ekaterina Rende, Mario Bottoni, Ugo Calvieri, Stefano Crisanti, Andrea Spaccapelo, Roberta |
author_sort | Arcidiacono, Paola |
collection | PubMed |
description | PURPOSE: Human melanoma is a highly aggressive incurable cancer due to intrinsic cellular resistance to apoptosis, reprogramming, proliferation and survival during tumour progression. Sulforaphane (SFN), an isothiocyanate found in cruciferous vegetables, plays a role in carcinogenesis in many cancer types. However, the cytotoxic molecular mechanisms and gene expression profiles promoted by SFN in human melanoma remain unknown. METHODS: Three different cell lines were used: two human melanoma A375 and 501MEL and human epidermal melanocytes (HEMa). Cell viability and proliferation, cell cycle analysis, cell migration and invasion and protein expression and phosphorylation status of Akt and p53 upon SFN treatment were determined. RNA-seq of A375 was performed at different time points after SFN treatment. RESULTS: We demonstrated that SFN strongly decreased cell viability and proliferation, induced G(2)/M cell cycle arrest, promoted apoptosis through the activation of caspases 3, 8, 9 and hampered migration and invasion abilities in the melanoma cell lines. Remarkably, HEMa cells were not affected by SFN treatment. Transcriptomic analysis revealed regulation of genes involved in response to stress, apoptosis/cell death and metabolic processes. SFN upregulated the expression of pro-apoptotic genes, such as p53, BAX, PUMA, FAS and MDM2; promoted cell cycle inhibition and growth arrest by upregulating EGR1, GADD45B, ATF3 and CDKN1A; and simultaneously acted as a potent inhibitor of genotoxicity by launching the stress-inducible protein network (HMOX1, HSPA1A, HSPA6, SOD1). CONCLUSION: Overall, the data show that SFN cytotoxicity in melanoma derives from complex and concurrent mechanisms during carcinogenesis, which makes it a promising cancer prevention agent. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00394-017-1527-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6182666 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-61826662018-10-24 Antitumor activity and expression profiles of genes induced by sulforaphane in human melanoma cells Arcidiacono, Paola Ragonese, Francesco Stabile, Anna Pistilli, Alessandra Kuligina, Ekaterina Rende, Mario Bottoni, Ugo Calvieri, Stefano Crisanti, Andrea Spaccapelo, Roberta Eur J Nutr Original Contribution PURPOSE: Human melanoma is a highly aggressive incurable cancer due to intrinsic cellular resistance to apoptosis, reprogramming, proliferation and survival during tumour progression. Sulforaphane (SFN), an isothiocyanate found in cruciferous vegetables, plays a role in carcinogenesis in many cancer types. However, the cytotoxic molecular mechanisms and gene expression profiles promoted by SFN in human melanoma remain unknown. METHODS: Three different cell lines were used: two human melanoma A375 and 501MEL and human epidermal melanocytes (HEMa). Cell viability and proliferation, cell cycle analysis, cell migration and invasion and protein expression and phosphorylation status of Akt and p53 upon SFN treatment were determined. RNA-seq of A375 was performed at different time points after SFN treatment. RESULTS: We demonstrated that SFN strongly decreased cell viability and proliferation, induced G(2)/M cell cycle arrest, promoted apoptosis through the activation of caspases 3, 8, 9 and hampered migration and invasion abilities in the melanoma cell lines. Remarkably, HEMa cells were not affected by SFN treatment. Transcriptomic analysis revealed regulation of genes involved in response to stress, apoptosis/cell death and metabolic processes. SFN upregulated the expression of pro-apoptotic genes, such as p53, BAX, PUMA, FAS and MDM2; promoted cell cycle inhibition and growth arrest by upregulating EGR1, GADD45B, ATF3 and CDKN1A; and simultaneously acted as a potent inhibitor of genotoxicity by launching the stress-inducible protein network (HMOX1, HSPA1A, HSPA6, SOD1). CONCLUSION: Overall, the data show that SFN cytotoxicity in melanoma derives from complex and concurrent mechanisms during carcinogenesis, which makes it a promising cancer prevention agent. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00394-017-1527-7) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2017-09-01 2018 /pmc/articles/PMC6182666/ /pubmed/28864908 http://dx.doi.org/10.1007/s00394-017-1527-7 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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. |
spellingShingle | Original Contribution Arcidiacono, Paola Ragonese, Francesco Stabile, Anna Pistilli, Alessandra Kuligina, Ekaterina Rende, Mario Bottoni, Ugo Calvieri, Stefano Crisanti, Andrea Spaccapelo, Roberta Antitumor activity and expression profiles of genes induced by sulforaphane in human melanoma cells |
title | Antitumor activity and expression profiles of genes induced by sulforaphane in human melanoma cells |
title_full | Antitumor activity and expression profiles of genes induced by sulforaphane in human melanoma cells |
title_fullStr | Antitumor activity and expression profiles of genes induced by sulforaphane in human melanoma cells |
title_full_unstemmed | Antitumor activity and expression profiles of genes induced by sulforaphane in human melanoma cells |
title_short | Antitumor activity and expression profiles of genes induced by sulforaphane in human melanoma cells |
title_sort | antitumor activity and expression profiles of genes induced by sulforaphane in human melanoma cells |
topic | Original Contribution |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6182666/ https://www.ncbi.nlm.nih.gov/pubmed/28864908 http://dx.doi.org/10.1007/s00394-017-1527-7 |
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