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The Dietary Isothiocyanate Erucin Reduces Kidney Cell Motility by Disturbing Tubulin Polymerization
SCOPE: Epidemiological evidence associates the consumption of cruciferous vegetables with reduced risk of several cancers, including renal cell carcinoma. Erucin can be generated by in vivo reduction of sulforaphane or by enzymatic hydrolysis of glucoerucin. Contrarily to sulforaphane, only limited...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10077903/ https://www.ncbi.nlm.nih.gov/pubmed/36415106 http://dx.doi.org/10.1002/mnfr.202200581 |
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author | Guerreiro, Íris Vidovic, Bojana Costa, João G. Martins, Marta Ferreira, Sandra Oliveira, Nuno G. Saraiva, Nuno Fernandes, Ana S. |
author_facet | Guerreiro, Íris Vidovic, Bojana Costa, João G. Martins, Marta Ferreira, Sandra Oliveira, Nuno G. Saraiva, Nuno Fernandes, Ana S. |
author_sort | Guerreiro, Íris |
collection | PubMed |
description | SCOPE: Epidemiological evidence associates the consumption of cruciferous vegetables with reduced risk of several cancers, including renal cell carcinoma. Erucin can be generated by in vivo reduction of sulforaphane or by enzymatic hydrolysis of glucoerucin. Contrarily to sulforaphane, only limited studies have addressed the anticancer properties of erucin. This study aims at evaluating the impact of erucin on renal cell biology. METHODS AND RESULTS: The effects of erucin were assessed in 786‐O and Vero‐E6 cells, representative of human renal cancer and non‐ cancer kidney cells, respectively. Erucin induced a concentration‐dependent decrease in cell viability and cell cycle arrest at G2/Mitosis. In Vero‐E6 cells erucin modestly reduced intracellular reactive oxygen species levels while in 786‐O no effects were detected. After erucin treatment, both cell lines revealed altered morphology, with a concentration‐dependent change from an elongated shape towards a smaller round conformation. Moreover, erucin affected cell adhesion and strongly altered the tubulin network structure and specifically microtubule polymerization. These results are in line with the observed decrease in collective and single cell migration and G2/Mitosis arrest. CONCLUSIONS: Overall, erucin may have a beneficial impact in reducing the motility of renal cancer cells. Our results contribute to explore possible dietary approaches for secondary/tertiary renal cancer chemoprevention. |
format | Online Article Text |
id | pubmed-10077903 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100779032023-04-07 The Dietary Isothiocyanate Erucin Reduces Kidney Cell Motility by Disturbing Tubulin Polymerization Guerreiro, Íris Vidovic, Bojana Costa, João G. Martins, Marta Ferreira, Sandra Oliveira, Nuno G. Saraiva, Nuno Fernandes, Ana S. Mol Nutr Food Res Research Articles SCOPE: Epidemiological evidence associates the consumption of cruciferous vegetables with reduced risk of several cancers, including renal cell carcinoma. Erucin can be generated by in vivo reduction of sulforaphane or by enzymatic hydrolysis of glucoerucin. Contrarily to sulforaphane, only limited studies have addressed the anticancer properties of erucin. This study aims at evaluating the impact of erucin on renal cell biology. METHODS AND RESULTS: The effects of erucin were assessed in 786‐O and Vero‐E6 cells, representative of human renal cancer and non‐ cancer kidney cells, respectively. Erucin induced a concentration‐dependent decrease in cell viability and cell cycle arrest at G2/Mitosis. In Vero‐E6 cells erucin modestly reduced intracellular reactive oxygen species levels while in 786‐O no effects were detected. After erucin treatment, both cell lines revealed altered morphology, with a concentration‐dependent change from an elongated shape towards a smaller round conformation. Moreover, erucin affected cell adhesion and strongly altered the tubulin network structure and specifically microtubule polymerization. These results are in line with the observed decrease in collective and single cell migration and G2/Mitosis arrest. CONCLUSIONS: Overall, erucin may have a beneficial impact in reducing the motility of renal cancer cells. Our results contribute to explore possible dietary approaches for secondary/tertiary renal cancer chemoprevention. John Wiley and Sons Inc. 2022-12-15 2023-02 /pmc/articles/PMC10077903/ /pubmed/36415106 http://dx.doi.org/10.1002/mnfr.202200581 Text en © 2022 The Authors. Molecular Nutrition & Food Research published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Guerreiro, Íris Vidovic, Bojana Costa, João G. Martins, Marta Ferreira, Sandra Oliveira, Nuno G. Saraiva, Nuno Fernandes, Ana S. The Dietary Isothiocyanate Erucin Reduces Kidney Cell Motility by Disturbing Tubulin Polymerization |
title | The Dietary Isothiocyanate Erucin Reduces Kidney Cell Motility by Disturbing Tubulin Polymerization |
title_full | The Dietary Isothiocyanate Erucin Reduces Kidney Cell Motility by Disturbing Tubulin Polymerization |
title_fullStr | The Dietary Isothiocyanate Erucin Reduces Kidney Cell Motility by Disturbing Tubulin Polymerization |
title_full_unstemmed | The Dietary Isothiocyanate Erucin Reduces Kidney Cell Motility by Disturbing Tubulin Polymerization |
title_short | The Dietary Isothiocyanate Erucin Reduces Kidney Cell Motility by Disturbing Tubulin Polymerization |
title_sort | dietary isothiocyanate erucin reduces kidney cell motility by disturbing tubulin polymerization |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10077903/ https://www.ncbi.nlm.nih.gov/pubmed/36415106 http://dx.doi.org/10.1002/mnfr.202200581 |
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