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Cannabidiol Inhibits the Proliferation and Invasiveness of Prostate Cancer Cells
[Image: see text] Prostate cancer is the fifth leading cause of cancer death in men, responsible for over 375,000 deaths in 2020. Novel therapeutic strategies are needed to improve outcomes. Cannabinoids, chemical components of the cannabis plant, are a possible solution. Preclinical evidence demons...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society and American Society of Pharmacognosy
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10521019/ https://www.ncbi.nlm.nih.gov/pubmed/37703852 http://dx.doi.org/10.1021/acs.jnatprod.3c00363 |
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author | O’Reilly, Eve Khalifa, Karima Cosgrave, Joanne Azam, Haleema Prencipe, Maria Simpson, Jeremy C. Gallagher, William M. Perry, Antoinette S. |
author_facet | O’Reilly, Eve Khalifa, Karima Cosgrave, Joanne Azam, Haleema Prencipe, Maria Simpson, Jeremy C. Gallagher, William M. Perry, Antoinette S. |
author_sort | O’Reilly, Eve |
collection | PubMed |
description | [Image: see text] Prostate cancer is the fifth leading cause of cancer death in men, responsible for over 375,000 deaths in 2020. Novel therapeutic strategies are needed to improve outcomes. Cannabinoids, chemical components of the cannabis plant, are a possible solution. Preclinical evidence demonstrates that cannabinoids can modulate several cancer hallmarks of many tumor types. However, the therapeutic potential of cannabinoids in prostate cancer has not yet been fully explored. The aim of this study was to investigate the antiproliferative and anti-invasive properties of cannabidiol (CBD) in prostate cancer cells in vitro. CBD inhibited cell viability and proliferation, accompanied by reduced expression of key cell cycle proteins, specifically cyclin D3 and cyclin-dependent kinases CDK2, CDK4, and CDK1, and inhibition of AKT phosphorylation. The effects of CBD on cell viability were not blocked by cannabinoid receptor antagonists, a transient receptor potential vanilloid 1 (TRPV1) channel blocker, or an agonist of the G-protein-coupled receptor GPR55, suggesting that CBD acts independently of these targets in prostate cancer cells. Furthermore, CBD reduced the invasiveness of highly metastatic PC-3 cells and increased protein expression of E-cadherin. The ability of CBD to inhibit prostate cancer cell proliferation and invasiveness suggests that CBD may have potential as a future chemotherapeutic agent. |
format | Online Article Text |
id | pubmed-10521019 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society and American Society of Pharmacognosy |
record_format | MEDLINE/PubMed |
spelling | pubmed-105210192023-09-27 Cannabidiol Inhibits the Proliferation and Invasiveness of Prostate Cancer Cells O’Reilly, Eve Khalifa, Karima Cosgrave, Joanne Azam, Haleema Prencipe, Maria Simpson, Jeremy C. Gallagher, William M. Perry, Antoinette S. J Nat Prod [Image: see text] Prostate cancer is the fifth leading cause of cancer death in men, responsible for over 375,000 deaths in 2020. Novel therapeutic strategies are needed to improve outcomes. Cannabinoids, chemical components of the cannabis plant, are a possible solution. Preclinical evidence demonstrates that cannabinoids can modulate several cancer hallmarks of many tumor types. However, the therapeutic potential of cannabinoids in prostate cancer has not yet been fully explored. The aim of this study was to investigate the antiproliferative and anti-invasive properties of cannabidiol (CBD) in prostate cancer cells in vitro. CBD inhibited cell viability and proliferation, accompanied by reduced expression of key cell cycle proteins, specifically cyclin D3 and cyclin-dependent kinases CDK2, CDK4, and CDK1, and inhibition of AKT phosphorylation. The effects of CBD on cell viability were not blocked by cannabinoid receptor antagonists, a transient receptor potential vanilloid 1 (TRPV1) channel blocker, or an agonist of the G-protein-coupled receptor GPR55, suggesting that CBD acts independently of these targets in prostate cancer cells. Furthermore, CBD reduced the invasiveness of highly metastatic PC-3 cells and increased protein expression of E-cadherin. The ability of CBD to inhibit prostate cancer cell proliferation and invasiveness suggests that CBD may have potential as a future chemotherapeutic agent. American Chemical Society and American Society of Pharmacognosy 2023-09-13 /pmc/articles/PMC10521019/ /pubmed/37703852 http://dx.doi.org/10.1021/acs.jnatprod.3c00363 Text en © 2023 The Authors. Published by American Chemical Society and American Society of Pharmacognosy https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | O’Reilly, Eve Khalifa, Karima Cosgrave, Joanne Azam, Haleema Prencipe, Maria Simpson, Jeremy C. Gallagher, William M. Perry, Antoinette S. Cannabidiol Inhibits the Proliferation and Invasiveness of Prostate Cancer Cells |
title | Cannabidiol
Inhibits the Proliferation and Invasiveness
of Prostate Cancer Cells |
title_full | Cannabidiol
Inhibits the Proliferation and Invasiveness
of Prostate Cancer Cells |
title_fullStr | Cannabidiol
Inhibits the Proliferation and Invasiveness
of Prostate Cancer Cells |
title_full_unstemmed | Cannabidiol
Inhibits the Proliferation and Invasiveness
of Prostate Cancer Cells |
title_short | Cannabidiol
Inhibits the Proliferation and Invasiveness
of Prostate Cancer Cells |
title_sort | cannabidiol
inhibits the proliferation and invasiveness
of prostate cancer cells |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10521019/ https://www.ncbi.nlm.nih.gov/pubmed/37703852 http://dx.doi.org/10.1021/acs.jnatprod.3c00363 |
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