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Breast cancer: Muscarinic receptors as new targets for tumor therapy
The development of breast cancer is a complex process that involves the participation of different factors. Several authors have demonstrated the overexpression of muscarinic acetylcholine receptors (mAChRs) in different tumor tissues and their role in the modulation of tumor biology, positioning th...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8223712/ https://www.ncbi.nlm.nih.gov/pubmed/34189066 http://dx.doi.org/10.5306/wjco.v12.i6.404 |
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author | Español, Alejandro Salem, Agustina Sanchez, Yamila Sales, María Elena |
author_facet | Español, Alejandro Salem, Agustina Sanchez, Yamila Sales, María Elena |
author_sort | Español, Alejandro |
collection | PubMed |
description | The development of breast cancer is a complex process that involves the participation of different factors. Several authors have demonstrated the overexpression of muscarinic acetylcholine receptors (mAChRs) in different tumor tissues and their role in the modulation of tumor biology, positioning them as therapeutic targets in cancer. The conventional treatment for breast cancer involves surgery, radiotherapy, and/or chemotherapy. The latter presents disadvantages such as limited specificity, the appearance of resistance to treatment and other side effects. To prevent these side effects, several schedules of drug administration, like metronomic therapy, have been developed. Metronomic therapy is a type of chemotherapy in which one or more drugs are administered at low concentrations repetitively. Recently, two chemotherapeutic agents usually used to treat breast cancer have been considered able to activate mAChRs. The combination of low concentrations of these chemotherapeutic agents with muscarinic agonists could be a useful option to be applied in breast cancer treatment, since this combination not only reduces tumor cell survival without affecting normal cells, but also decreases pathological neo-angiogenesis, the expression of drug extrusion proteins and the cancer stem cell fraction. In this review, we focus on the previous evidences that have positioned mAChRs as relevant therapeutic targets in breast cancer and analyze the effects of administering muscarinic agonists in combination with conventional chemotherapeutic agents in a metronomic schedule. |
format | Online Article Text |
id | pubmed-8223712 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-82237122021-06-28 Breast cancer: Muscarinic receptors as new targets for tumor therapy Español, Alejandro Salem, Agustina Sanchez, Yamila Sales, María Elena World J Clin Oncol Review The development of breast cancer is a complex process that involves the participation of different factors. Several authors have demonstrated the overexpression of muscarinic acetylcholine receptors (mAChRs) in different tumor tissues and their role in the modulation of tumor biology, positioning them as therapeutic targets in cancer. The conventional treatment for breast cancer involves surgery, radiotherapy, and/or chemotherapy. The latter presents disadvantages such as limited specificity, the appearance of resistance to treatment and other side effects. To prevent these side effects, several schedules of drug administration, like metronomic therapy, have been developed. Metronomic therapy is a type of chemotherapy in which one or more drugs are administered at low concentrations repetitively. Recently, two chemotherapeutic agents usually used to treat breast cancer have been considered able to activate mAChRs. The combination of low concentrations of these chemotherapeutic agents with muscarinic agonists could be a useful option to be applied in breast cancer treatment, since this combination not only reduces tumor cell survival without affecting normal cells, but also decreases pathological neo-angiogenesis, the expression of drug extrusion proteins and the cancer stem cell fraction. In this review, we focus on the previous evidences that have positioned mAChRs as relevant therapeutic targets in breast cancer and analyze the effects of administering muscarinic agonists in combination with conventional chemotherapeutic agents in a metronomic schedule. Baishideng Publishing Group Inc 2021-06-24 2021-06-24 /pmc/articles/PMC8223712/ /pubmed/34189066 http://dx.doi.org/10.5306/wjco.v12.i6.404 Text en ©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/Licenses/by-nc/4.0/ |
spellingShingle | Review Español, Alejandro Salem, Agustina Sanchez, Yamila Sales, María Elena Breast cancer: Muscarinic receptors as new targets for tumor therapy |
title | Breast cancer: Muscarinic receptors as new targets for tumor therapy |
title_full | Breast cancer: Muscarinic receptors as new targets for tumor therapy |
title_fullStr | Breast cancer: Muscarinic receptors as new targets for tumor therapy |
title_full_unstemmed | Breast cancer: Muscarinic receptors as new targets for tumor therapy |
title_short | Breast cancer: Muscarinic receptors as new targets for tumor therapy |
title_sort | breast cancer: muscarinic receptors as new targets for tumor therapy |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8223712/ https://www.ncbi.nlm.nih.gov/pubmed/34189066 http://dx.doi.org/10.5306/wjco.v12.i6.404 |
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