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Anti-proliferative and cytotoxic effect of cannabidiol on human cancer cell lines in presence of serum
OBJECTIVE: Cannabinoids are able to reduce tumor growth in xenograft models, but their therapeutic potential as anti-cancer drugs in humans is unclear yet. In vitro studies of the effect of cannabinoids on cancer cells are often carried out in absence of serum or in low serum concentration (i.e. 0.5...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7441616/ https://www.ncbi.nlm.nih.gov/pubmed/32819436 http://dx.doi.org/10.1186/s13104-020-05229-5 |
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author | Sainz-Cort, Alberto Müller-Sánchez, Claudia Espel, Enric |
author_facet | Sainz-Cort, Alberto Müller-Sánchez, Claudia Espel, Enric |
author_sort | Sainz-Cort, Alberto |
collection | PubMed |
description | OBJECTIVE: Cannabinoids are able to reduce tumor growth in xenograft models, but their therapeutic potential as anti-cancer drugs in humans is unclear yet. In vitro studies of the effect of cannabinoids on cancer cells are often carried out in absence of serum or in low serum concentration (i.e. 0.5% serum), conditions that limit cellular growth and therefore can increase the response of cells to additional challenges such as the presence of cannabinoids. However, the tumor microenvironment can be teaming with growth factors. In this study we assessed the viability and proliferation of cancer cells treated with cannabidiol in presence of a serum concentration that commonly sustains cell growth (10% serum). RESULTS: The results show that cannabidiol exerts a markedly different effect on the viability of the human HT-29 cancer cell line when cultured in presence of 0.5% serum in comparison to 10% serum, displaying a cytotoxic effect only in the former situation. In presence of 10% serum, no inhibitory effect of cannabidiol on DNA replication of HT-29 cells was detected, and a weak inhibition was observed for other cancer cell lines. These results indicate that the effect of cannabidiol is cell context-dependent being modulated by the presence of growth factors. |
format | Online Article Text |
id | pubmed-7441616 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-74416162020-08-24 Anti-proliferative and cytotoxic effect of cannabidiol on human cancer cell lines in presence of serum Sainz-Cort, Alberto Müller-Sánchez, Claudia Espel, Enric BMC Res Notes Research Note OBJECTIVE: Cannabinoids are able to reduce tumor growth in xenograft models, but their therapeutic potential as anti-cancer drugs in humans is unclear yet. In vitro studies of the effect of cannabinoids on cancer cells are often carried out in absence of serum or in low serum concentration (i.e. 0.5% serum), conditions that limit cellular growth and therefore can increase the response of cells to additional challenges such as the presence of cannabinoids. However, the tumor microenvironment can be teaming with growth factors. In this study we assessed the viability and proliferation of cancer cells treated with cannabidiol in presence of a serum concentration that commonly sustains cell growth (10% serum). RESULTS: The results show that cannabidiol exerts a markedly different effect on the viability of the human HT-29 cancer cell line when cultured in presence of 0.5% serum in comparison to 10% serum, displaying a cytotoxic effect only in the former situation. In presence of 10% serum, no inhibitory effect of cannabidiol on DNA replication of HT-29 cells was detected, and a weak inhibition was observed for other cancer cell lines. These results indicate that the effect of cannabidiol is cell context-dependent being modulated by the presence of growth factors. BioMed Central 2020-08-20 /pmc/articles/PMC7441616/ /pubmed/32819436 http://dx.doi.org/10.1186/s13104-020-05229-5 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Note Sainz-Cort, Alberto Müller-Sánchez, Claudia Espel, Enric Anti-proliferative and cytotoxic effect of cannabidiol on human cancer cell lines in presence of serum |
title | Anti-proliferative and cytotoxic effect of cannabidiol on human cancer cell lines in presence of serum |
title_full | Anti-proliferative and cytotoxic effect of cannabidiol on human cancer cell lines in presence of serum |
title_fullStr | Anti-proliferative and cytotoxic effect of cannabidiol on human cancer cell lines in presence of serum |
title_full_unstemmed | Anti-proliferative and cytotoxic effect of cannabidiol on human cancer cell lines in presence of serum |
title_short | Anti-proliferative and cytotoxic effect of cannabidiol on human cancer cell lines in presence of serum |
title_sort | anti-proliferative and cytotoxic effect of cannabidiol on human cancer cell lines in presence of serum |
topic | Research Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7441616/ https://www.ncbi.nlm.nih.gov/pubmed/32819436 http://dx.doi.org/10.1186/s13104-020-05229-5 |
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