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Synthetic Cannabinoid Activity Against Colorectal Cancer Cells
Introduction: Colorectal cancer (CRC) is a leading cause of cancer-related deaths worldwide, and new therapeutic strategies are still required. Here we screened a synthetic cannabinoid library to identify compounds that uniformly reduce the viability of seven CRC cell lines. Material and Methods: Se...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mary Ann Liebert, Inc., publishers
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6340378/ https://www.ncbi.nlm.nih.gov/pubmed/30671539 http://dx.doi.org/10.1089/can.2018.0065 |
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author | Raup-Konsavage, Wesley M. Johnson, Megan Legare, Christopher A. Yochum, Gregory S. Morgan, Daniel J. Vrana, Kent E. |
author_facet | Raup-Konsavage, Wesley M. Johnson, Megan Legare, Christopher A. Yochum, Gregory S. Morgan, Daniel J. Vrana, Kent E. |
author_sort | Raup-Konsavage, Wesley M. |
collection | PubMed |
description | Introduction: Colorectal cancer (CRC) is a leading cause of cancer-related deaths worldwide, and new therapeutic strategies are still required. Here we screened a synthetic cannabinoid library to identify compounds that uniformly reduce the viability of seven CRC cell lines. Material and Methods: Seven distinct CRC cell lines were treated with 10 μM cannabinoid compounds (from a library of 370 molecules) for 48 h, and cell viability was subsequently measured with MTS assay. Dose–response curves were conducted for compounds that were found to reproducibly reduce cell viability of one or more cell lines. Results: We identified 10 compounds from the library that were able to reduce cell viability of CRC cell lines (with an IC(50) ≤ 30 μM). Of these compounds, seven were specific for CRC cells, and six were effective in all CRC cell lines tested. Treatment with traditional phytocannabinoids (THC or CBD) was either ineffective or much less potent and only partially efficacious. Treatment with antagonists for the known cannabinoid receptors (alone or in combination) failed to block the activity of the most potent of identified compounds. Conclusion: We identified three families of cannabinoid compounds that reduce CRC cell viability through a noncanonical receptor mechanism. Future modification of these compounds may lead to the development of novel therapies to treat this disease. |
format | Online Article Text |
id | pubmed-6340378 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Mary Ann Liebert, Inc., publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-63403782019-01-22 Synthetic Cannabinoid Activity Against Colorectal Cancer Cells Raup-Konsavage, Wesley M. Johnson, Megan Legare, Christopher A. Yochum, Gregory S. Morgan, Daniel J. Vrana, Kent E. Cannabis Cannabinoid Res Original Research Introduction: Colorectal cancer (CRC) is a leading cause of cancer-related deaths worldwide, and new therapeutic strategies are still required. Here we screened a synthetic cannabinoid library to identify compounds that uniformly reduce the viability of seven CRC cell lines. Material and Methods: Seven distinct CRC cell lines were treated with 10 μM cannabinoid compounds (from a library of 370 molecules) for 48 h, and cell viability was subsequently measured with MTS assay. Dose–response curves were conducted for compounds that were found to reproducibly reduce cell viability of one or more cell lines. Results: We identified 10 compounds from the library that were able to reduce cell viability of CRC cell lines (with an IC(50) ≤ 30 μM). Of these compounds, seven were specific for CRC cells, and six were effective in all CRC cell lines tested. Treatment with traditional phytocannabinoids (THC or CBD) was either ineffective or much less potent and only partially efficacious. Treatment with antagonists for the known cannabinoid receptors (alone or in combination) failed to block the activity of the most potent of identified compounds. Conclusion: We identified three families of cannabinoid compounds that reduce CRC cell viability through a noncanonical receptor mechanism. Future modification of these compounds may lead to the development of novel therapies to treat this disease. Mary Ann Liebert, Inc., publishers 2018-12-21 /pmc/articles/PMC6340378/ /pubmed/30671539 http://dx.doi.org/10.1089/can.2018.0065 Text en © Wesley M. Raup-Konsavage et al. 2018; Published by Mary Ann Liebert, Inc. This Open Access article is distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Raup-Konsavage, Wesley M. Johnson, Megan Legare, Christopher A. Yochum, Gregory S. Morgan, Daniel J. Vrana, Kent E. Synthetic Cannabinoid Activity Against Colorectal Cancer Cells |
title | Synthetic Cannabinoid Activity Against Colorectal Cancer Cells |
title_full | Synthetic Cannabinoid Activity Against Colorectal Cancer Cells |
title_fullStr | Synthetic Cannabinoid Activity Against Colorectal Cancer Cells |
title_full_unstemmed | Synthetic Cannabinoid Activity Against Colorectal Cancer Cells |
title_short | Synthetic Cannabinoid Activity Against Colorectal Cancer Cells |
title_sort | synthetic cannabinoid activity against colorectal cancer cells |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6340378/ https://www.ncbi.nlm.nih.gov/pubmed/30671539 http://dx.doi.org/10.1089/can.2018.0065 |
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