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Combination of Heme Oxygenase-1 Inhibition and Sigma Receptor Modulation for Anticancer Activity
Cancer is a multifactorial disease that may be tackled by targeting different signaling pathways. Heme oxygenase-1 (HO-1) and sigma receptors (σRs) are both overexpressed in different human cancers, including prostate and brain, contributing to the cancer spreading. In the present study, we investig...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8270315/ https://www.ncbi.nlm.nih.gov/pubmed/34202711 http://dx.doi.org/10.3390/molecules26133860 |
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author | Romeo, Giuseppe Ciaffaglione, Valeria Amata, Emanuele Dichiara, Maria Calabrese, Loredana Vanella, Luca Sorrenti, Valeria Grosso, Salvo D’Amico, Agata Grazia D’Agata, Velia Intagliata, Sebastiano Salerno, Loredana |
author_facet | Romeo, Giuseppe Ciaffaglione, Valeria Amata, Emanuele Dichiara, Maria Calabrese, Loredana Vanella, Luca Sorrenti, Valeria Grosso, Salvo D’Amico, Agata Grazia D’Agata, Velia Intagliata, Sebastiano Salerno, Loredana |
author_sort | Romeo, Giuseppe |
collection | PubMed |
description | Cancer is a multifactorial disease that may be tackled by targeting different signaling pathways. Heme oxygenase-1 (HO-1) and sigma receptors (σRs) are both overexpressed in different human cancers, including prostate and brain, contributing to the cancer spreading. In the present study, we investigated whether HO-1 inhibitors and σR ligands, as well a combination of the two, may influence DU145 human prostate and U87MG human glioblastoma cancer cells proliferation. In addition, we synthesized, characterized, and tested a small series of novel hybrid compounds (HO-1/σRs) 1–4 containing the chemical features needed for HO-1 inhibition and σR modulation. Herein, we report for the first time that targeting simultaneously HO-1 and σR proteins may be a good strategy to achieve increased antiproliferative activity against DU145 and U87MG cells, with respect to the mono administration of the parent compounds. The obtained outcomes provide an initial proof of concept useful to further optimize the structure of HO-1/σRs hybrids to develop novel potential anticancer agents. |
format | Online Article Text |
id | pubmed-8270315 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-82703152021-07-10 Combination of Heme Oxygenase-1 Inhibition and Sigma Receptor Modulation for Anticancer Activity Romeo, Giuseppe Ciaffaglione, Valeria Amata, Emanuele Dichiara, Maria Calabrese, Loredana Vanella, Luca Sorrenti, Valeria Grosso, Salvo D’Amico, Agata Grazia D’Agata, Velia Intagliata, Sebastiano Salerno, Loredana Molecules Communication Cancer is a multifactorial disease that may be tackled by targeting different signaling pathways. Heme oxygenase-1 (HO-1) and sigma receptors (σRs) are both overexpressed in different human cancers, including prostate and brain, contributing to the cancer spreading. In the present study, we investigated whether HO-1 inhibitors and σR ligands, as well a combination of the two, may influence DU145 human prostate and U87MG human glioblastoma cancer cells proliferation. In addition, we synthesized, characterized, and tested a small series of novel hybrid compounds (HO-1/σRs) 1–4 containing the chemical features needed for HO-1 inhibition and σR modulation. Herein, we report for the first time that targeting simultaneously HO-1 and σR proteins may be a good strategy to achieve increased antiproliferative activity against DU145 and U87MG cells, with respect to the mono administration of the parent compounds. The obtained outcomes provide an initial proof of concept useful to further optimize the structure of HO-1/σRs hybrids to develop novel potential anticancer agents. MDPI 2021-06-24 /pmc/articles/PMC8270315/ /pubmed/34202711 http://dx.doi.org/10.3390/molecules26133860 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Romeo, Giuseppe Ciaffaglione, Valeria Amata, Emanuele Dichiara, Maria Calabrese, Loredana Vanella, Luca Sorrenti, Valeria Grosso, Salvo D’Amico, Agata Grazia D’Agata, Velia Intagliata, Sebastiano Salerno, Loredana Combination of Heme Oxygenase-1 Inhibition and Sigma Receptor Modulation for Anticancer Activity |
title | Combination of Heme Oxygenase-1 Inhibition and Sigma Receptor Modulation for Anticancer Activity |
title_full | Combination of Heme Oxygenase-1 Inhibition and Sigma Receptor Modulation for Anticancer Activity |
title_fullStr | Combination of Heme Oxygenase-1 Inhibition and Sigma Receptor Modulation for Anticancer Activity |
title_full_unstemmed | Combination of Heme Oxygenase-1 Inhibition and Sigma Receptor Modulation for Anticancer Activity |
title_short | Combination of Heme Oxygenase-1 Inhibition and Sigma Receptor Modulation for Anticancer Activity |
title_sort | combination of heme oxygenase-1 inhibition and sigma receptor modulation for anticancer activity |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8270315/ https://www.ncbi.nlm.nih.gov/pubmed/34202711 http://dx.doi.org/10.3390/molecules26133860 |
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