Cargando…

Future Aspects for Cannabinoids in Breast Cancer Therapy

Cannabinoids (CBs) from Cannabis sativa provide relief for tumor-associated symptoms (including nausea, anorexia, and neuropathic pain) in the palliative treatment of cancer patients. Additionally, they may decelerate tumor progression in breast cancer patients. Indeed, the psychoactive delta-9-tetr...

Descripción completa

Detalles Bibliográficos
Autores principales: Kisková, Terézia, Mungenast, Felicitas, Suváková, Mária, Jäger, Walter, Thalhammer, Theresia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6479799/
https://www.ncbi.nlm.nih.gov/pubmed/30987191
http://dx.doi.org/10.3390/ijms20071673
_version_ 1783413428496367616
author Kisková, Terézia
Mungenast, Felicitas
Suváková, Mária
Jäger, Walter
Thalhammer, Theresia
author_facet Kisková, Terézia
Mungenast, Felicitas
Suváková, Mária
Jäger, Walter
Thalhammer, Theresia
author_sort Kisková, Terézia
collection PubMed
description Cannabinoids (CBs) from Cannabis sativa provide relief for tumor-associated symptoms (including nausea, anorexia, and neuropathic pain) in the palliative treatment of cancer patients. Additionally, they may decelerate tumor progression in breast cancer patients. Indeed, the psychoactive delta-9-tetrahydrocannabinol (THC), non-psychoactive cannabidiol (CBD) and other CBs inhibited disease progression in breast cancer models. The effects of CBs on signaling pathways in cancer cells are conferred via G-protein coupled CB-receptors (CB-Rs), CB1-R and CB2-R, but also via other receptors, and in a receptor-independent way. THC is a partial agonist for CB1-R and CB2-R; CBD is an inverse agonist for both. In breast cancer, CB1-R expression is moderate, but CB2-R expression is high, which is related to tumor aggressiveness. CBs block cell cycle progression and cell growth and induce cancer cell apoptosis by inhibiting constitutive active pro-oncogenic signaling pathways, such as the extracellular-signal-regulated kinase pathway. They reduce angiogenesis and tumor metastasis in animal breast cancer models. CBs are not only active against estrogen receptor-positive, but also against estrogen-resistant breast cancer cells. In human epidermal growth factor receptor 2-positive and triple-negative breast cancer cells, blocking protein kinase B- and cyclooxygenase-2 signaling via CB2-R prevents tumor progression and metastasis. Furthermore, selective estrogen receptor modulators (SERMs), including tamoxifen, bind to CB-Rs; this process may contribute to the growth inhibitory effect of SERMs in cancer cells lacking the estrogen receptor. In summary, CBs are already administered to breast cancer patients at advanced stages of the disease, but they might also be effective at earlier stages to decelerate tumor progression.
format Online
Article
Text
id pubmed-6479799
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-64797992019-04-29 Future Aspects for Cannabinoids in Breast Cancer Therapy Kisková, Terézia Mungenast, Felicitas Suváková, Mária Jäger, Walter Thalhammer, Theresia Int J Mol Sci Review Cannabinoids (CBs) from Cannabis sativa provide relief for tumor-associated symptoms (including nausea, anorexia, and neuropathic pain) in the palliative treatment of cancer patients. Additionally, they may decelerate tumor progression in breast cancer patients. Indeed, the psychoactive delta-9-tetrahydrocannabinol (THC), non-psychoactive cannabidiol (CBD) and other CBs inhibited disease progression in breast cancer models. The effects of CBs on signaling pathways in cancer cells are conferred via G-protein coupled CB-receptors (CB-Rs), CB1-R and CB2-R, but also via other receptors, and in a receptor-independent way. THC is a partial agonist for CB1-R and CB2-R; CBD is an inverse agonist for both. In breast cancer, CB1-R expression is moderate, but CB2-R expression is high, which is related to tumor aggressiveness. CBs block cell cycle progression and cell growth and induce cancer cell apoptosis by inhibiting constitutive active pro-oncogenic signaling pathways, such as the extracellular-signal-regulated kinase pathway. They reduce angiogenesis and tumor metastasis in animal breast cancer models. CBs are not only active against estrogen receptor-positive, but also against estrogen-resistant breast cancer cells. In human epidermal growth factor receptor 2-positive and triple-negative breast cancer cells, blocking protein kinase B- and cyclooxygenase-2 signaling via CB2-R prevents tumor progression and metastasis. Furthermore, selective estrogen receptor modulators (SERMs), including tamoxifen, bind to CB-Rs; this process may contribute to the growth inhibitory effect of SERMs in cancer cells lacking the estrogen receptor. In summary, CBs are already administered to breast cancer patients at advanced stages of the disease, but they might also be effective at earlier stages to decelerate tumor progression. MDPI 2019-04-03 /pmc/articles/PMC6479799/ /pubmed/30987191 http://dx.doi.org/10.3390/ijms20071673 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 Review
Kisková, Terézia
Mungenast, Felicitas
Suváková, Mária
Jäger, Walter
Thalhammer, Theresia
Future Aspects for Cannabinoids in Breast Cancer Therapy
title Future Aspects for Cannabinoids in Breast Cancer Therapy
title_full Future Aspects for Cannabinoids in Breast Cancer Therapy
title_fullStr Future Aspects for Cannabinoids in Breast Cancer Therapy
title_full_unstemmed Future Aspects for Cannabinoids in Breast Cancer Therapy
title_short Future Aspects for Cannabinoids in Breast Cancer Therapy
title_sort future aspects for cannabinoids in breast cancer therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6479799/
https://www.ncbi.nlm.nih.gov/pubmed/30987191
http://dx.doi.org/10.3390/ijms20071673
work_keys_str_mv AT kiskovaterezia futureaspectsforcannabinoidsinbreastcancertherapy
AT mungenastfelicitas futureaspectsforcannabinoidsinbreastcancertherapy
AT suvakovamaria futureaspectsforcannabinoidsinbreastcancertherapy
AT jagerwalter futureaspectsforcannabinoidsinbreastcancertherapy
AT thalhammertheresia futureaspectsforcannabinoidsinbreastcancertherapy