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Calcitriol Inhibits Viability and Proliferation in Human Malignant Pleural Mesothelioma Cells

Malignant pleural mesothelioma (MPM) is a rare and aggressive tumor, often associated with exposure to asbestos and characterized by poor prognosis and limited treatment options. The biologically active form of vitamin D, calcitriol, exerts anticancer effects in many cell types, both alone and in co...

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Autores principales: Gesmundo, Iacopo, Silvagno, Francesca, Banfi, Dana, Monica, Valentina, Fanciulli, Alessandro, Gamba, Giacomo, Congiusta, Noemi, Libener, Roberta, Riganti, Chiara, Ghigo, Ezio, Granata, Riccarda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7579995/
https://www.ncbi.nlm.nih.gov/pubmed/33133014
http://dx.doi.org/10.3389/fendo.2020.559586
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author Gesmundo, Iacopo
Silvagno, Francesca
Banfi, Dana
Monica, Valentina
Fanciulli, Alessandro
Gamba, Giacomo
Congiusta, Noemi
Libener, Roberta
Riganti, Chiara
Ghigo, Ezio
Granata, Riccarda
author_facet Gesmundo, Iacopo
Silvagno, Francesca
Banfi, Dana
Monica, Valentina
Fanciulli, Alessandro
Gamba, Giacomo
Congiusta, Noemi
Libener, Roberta
Riganti, Chiara
Ghigo, Ezio
Granata, Riccarda
author_sort Gesmundo, Iacopo
collection PubMed
description Malignant pleural mesothelioma (MPM) is a rare and aggressive tumor, often associated with exposure to asbestos and characterized by poor prognosis and limited treatment options. The biologically active form of vitamin D, calcitriol, exerts anticancer effects in many cell types, both alone and in combination with chemotherapy drugs, through binding to vitamin D receptor (VDR); however, the role of calcitriol in MPM is still unknown. This study aimed to determine the potential antitumor role of calcitriol in MPM. The results showed that calcitriol reduces cell viability and proliferation in human MPM cells lines, which express both cytoplasmic and nuclear VDR; furthermore, calcitriol potentiated the inhibitory activity of the chemotherapy drug PEM. These effects were paralleled by cell cycle arrest and inhibition in expression of c-Myc and cyclins involved in cell cycle progression. Exposure of MPM cells to calcitriol also produced an alteration in mitochondrial function and inhibition in the expression of respiratory chain complex subunits. Finally, the inhibitory effects of calcitriol were also observed on viability of human primary MPM cells. Collectively, these results indicate a novel anticancer role for calcitriol in MPM, suggesting potential for vitamin D derivatives, alone or in combination with chemotherapy, in the treatment of this malignancy.
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spelling pubmed-75799952020-10-30 Calcitriol Inhibits Viability and Proliferation in Human Malignant Pleural Mesothelioma Cells Gesmundo, Iacopo Silvagno, Francesca Banfi, Dana Monica, Valentina Fanciulli, Alessandro Gamba, Giacomo Congiusta, Noemi Libener, Roberta Riganti, Chiara Ghigo, Ezio Granata, Riccarda Front Endocrinol (Lausanne) Endocrinology Malignant pleural mesothelioma (MPM) is a rare and aggressive tumor, often associated with exposure to asbestos and characterized by poor prognosis and limited treatment options. The biologically active form of vitamin D, calcitriol, exerts anticancer effects in many cell types, both alone and in combination with chemotherapy drugs, through binding to vitamin D receptor (VDR); however, the role of calcitriol in MPM is still unknown. This study aimed to determine the potential antitumor role of calcitriol in MPM. The results showed that calcitriol reduces cell viability and proliferation in human MPM cells lines, which express both cytoplasmic and nuclear VDR; furthermore, calcitriol potentiated the inhibitory activity of the chemotherapy drug PEM. These effects were paralleled by cell cycle arrest and inhibition in expression of c-Myc and cyclins involved in cell cycle progression. Exposure of MPM cells to calcitriol also produced an alteration in mitochondrial function and inhibition in the expression of respiratory chain complex subunits. Finally, the inhibitory effects of calcitriol were also observed on viability of human primary MPM cells. Collectively, these results indicate a novel anticancer role for calcitriol in MPM, suggesting potential for vitamin D derivatives, alone or in combination with chemotherapy, in the treatment of this malignancy. Frontiers Media S.A. 2020-10-08 /pmc/articles/PMC7579995/ /pubmed/33133014 http://dx.doi.org/10.3389/fendo.2020.559586 Text en Copyright © 2020 Gesmundo, Silvagno, Banfi, Monica, Fanciulli, Gamba, Congiusta, Libener, Riganti, Ghigo and Granata. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Gesmundo, Iacopo
Silvagno, Francesca
Banfi, Dana
Monica, Valentina
Fanciulli, Alessandro
Gamba, Giacomo
Congiusta, Noemi
Libener, Roberta
Riganti, Chiara
Ghigo, Ezio
Granata, Riccarda
Calcitriol Inhibits Viability and Proliferation in Human Malignant Pleural Mesothelioma Cells
title Calcitriol Inhibits Viability and Proliferation in Human Malignant Pleural Mesothelioma Cells
title_full Calcitriol Inhibits Viability and Proliferation in Human Malignant Pleural Mesothelioma Cells
title_fullStr Calcitriol Inhibits Viability and Proliferation in Human Malignant Pleural Mesothelioma Cells
title_full_unstemmed Calcitriol Inhibits Viability and Proliferation in Human Malignant Pleural Mesothelioma Cells
title_short Calcitriol Inhibits Viability and Proliferation in Human Malignant Pleural Mesothelioma Cells
title_sort calcitriol inhibits viability and proliferation in human malignant pleural mesothelioma cells
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7579995/
https://www.ncbi.nlm.nih.gov/pubmed/33133014
http://dx.doi.org/10.3389/fendo.2020.559586
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