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7-epi-Clusianone, a Multi-Targeting Natural Product with Potential Chemotherapeutic, Immune-Modulating, and Anti-Angiogenic Properties

Targeted therapies have changed the treatment of cancer, giving new hope to many patients in recent years. The shortcomings of targeted therapies including acquired resistance, limited susceptible patients, high cost, and high toxicities, have led to the necessity of combining these therapies with o...

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Autores principales: Taylor, Wesley F., Yanez, Maria, Moghadam, Sara E., Moridi Farimani, Mahdi, Soroury, Sara, Ebrahimi, Samad N., Tabefam, Marzieh, Jabbarzadeh, Ehsan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6930650/
https://www.ncbi.nlm.nih.gov/pubmed/31816878
http://dx.doi.org/10.3390/molecules24234415
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author Taylor, Wesley F.
Yanez, Maria
Moghadam, Sara E.
Moridi Farimani, Mahdi
Soroury, Sara
Ebrahimi, Samad N.
Tabefam, Marzieh
Jabbarzadeh, Ehsan
author_facet Taylor, Wesley F.
Yanez, Maria
Moghadam, Sara E.
Moridi Farimani, Mahdi
Soroury, Sara
Ebrahimi, Samad N.
Tabefam, Marzieh
Jabbarzadeh, Ehsan
author_sort Taylor, Wesley F.
collection PubMed
description Targeted therapies have changed the treatment of cancer, giving new hope to many patients in recent years. The shortcomings of targeted therapies including acquired resistance, limited susceptible patients, high cost, and high toxicities, have led to the necessity of combining these therapies with other targeted or chemotherapeutic treatments. Natural products are uniquely capable of synergizing with targeted and non-targeted anticancer regimens due to their ability to affect multiple cellular pathways simultaneously. Compounds which provide an additive effect to the often combined immune therapies and cytotoxic chemotherapies, are exceedingly rare. These compounds would however provide a strengthening bridge between the two treatment modalities, increasing their effectiveness and improving patient prognoses. In this study, 7-epi-clusianone was investigated for its anticancer properties. While previous studies have suggested clusianone and its conformational isomers, including 7-epi-clusianone, are chemotherapeutic, few cancer types have been demonstrated to exhibit sensitivity to these compounds and little is known about the mechanism. In this study, 7-epi-clusianone was shown to inhibit the growth of 60 cancer cell types and induce significant cell death in 25 cancer cell lines, while simultaneously modulating the immune system, inhibiting angiogenesis, and inhibiting cancer cell invasion, making it a promising lead compound for cancer drug discovery.
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spelling pubmed-69306502019-12-26 7-epi-Clusianone, a Multi-Targeting Natural Product with Potential Chemotherapeutic, Immune-Modulating, and Anti-Angiogenic Properties Taylor, Wesley F. Yanez, Maria Moghadam, Sara E. Moridi Farimani, Mahdi Soroury, Sara Ebrahimi, Samad N. Tabefam, Marzieh Jabbarzadeh, Ehsan Molecules Article Targeted therapies have changed the treatment of cancer, giving new hope to many patients in recent years. The shortcomings of targeted therapies including acquired resistance, limited susceptible patients, high cost, and high toxicities, have led to the necessity of combining these therapies with other targeted or chemotherapeutic treatments. Natural products are uniquely capable of synergizing with targeted and non-targeted anticancer regimens due to their ability to affect multiple cellular pathways simultaneously. Compounds which provide an additive effect to the often combined immune therapies and cytotoxic chemotherapies, are exceedingly rare. These compounds would however provide a strengthening bridge between the two treatment modalities, increasing their effectiveness and improving patient prognoses. In this study, 7-epi-clusianone was investigated for its anticancer properties. While previous studies have suggested clusianone and its conformational isomers, including 7-epi-clusianone, are chemotherapeutic, few cancer types have been demonstrated to exhibit sensitivity to these compounds and little is known about the mechanism. In this study, 7-epi-clusianone was shown to inhibit the growth of 60 cancer cell types and induce significant cell death in 25 cancer cell lines, while simultaneously modulating the immune system, inhibiting angiogenesis, and inhibiting cancer cell invasion, making it a promising lead compound for cancer drug discovery. MDPI 2019-12-03 /pmc/articles/PMC6930650/ /pubmed/31816878 http://dx.doi.org/10.3390/molecules24234415 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Taylor, Wesley F.
Yanez, Maria
Moghadam, Sara E.
Moridi Farimani, Mahdi
Soroury, Sara
Ebrahimi, Samad N.
Tabefam, Marzieh
Jabbarzadeh, Ehsan
7-epi-Clusianone, a Multi-Targeting Natural Product with Potential Chemotherapeutic, Immune-Modulating, and Anti-Angiogenic Properties
title 7-epi-Clusianone, a Multi-Targeting Natural Product with Potential Chemotherapeutic, Immune-Modulating, and Anti-Angiogenic Properties
title_full 7-epi-Clusianone, a Multi-Targeting Natural Product with Potential Chemotherapeutic, Immune-Modulating, and Anti-Angiogenic Properties
title_fullStr 7-epi-Clusianone, a Multi-Targeting Natural Product with Potential Chemotherapeutic, Immune-Modulating, and Anti-Angiogenic Properties
title_full_unstemmed 7-epi-Clusianone, a Multi-Targeting Natural Product with Potential Chemotherapeutic, Immune-Modulating, and Anti-Angiogenic Properties
title_short 7-epi-Clusianone, a Multi-Targeting Natural Product with Potential Chemotherapeutic, Immune-Modulating, and Anti-Angiogenic Properties
title_sort 7-epi-clusianone, a multi-targeting natural product with potential chemotherapeutic, immune-modulating, and anti-angiogenic properties
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6930650/
https://www.ncbi.nlm.nih.gov/pubmed/31816878
http://dx.doi.org/10.3390/molecules24234415
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