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Beta-adrenergic receptors are expressed across diverse cancers
Based largely on retrospective analyses and a handful of prospective case reports, pharmacological inhibition of the beta adrenergic receptors using beta blockers has shown clinical anti-cancer efficacy in reproductive cancers, as well as angiosarcoma and multiple myeloma. Because of the potential p...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5616202/ https://www.ncbi.nlm.nih.gov/pubmed/28966942 http://dx.doi.org/10.18632/oncoscience.357 |
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author | Rains, Steven L. Amaya, Clarissa N. Bryan, Brad A. |
author_facet | Rains, Steven L. Amaya, Clarissa N. Bryan, Brad A. |
author_sort | Rains, Steven L. |
collection | PubMed |
description | Based largely on retrospective analyses and a handful of prospective case reports, pharmacological inhibition of the beta adrenergic receptors using beta blockers has shown clinical anti-cancer efficacy in reproductive cancers, as well as angiosarcoma and multiple myeloma. Because of the potential promise of beta blockers as an adjunct to standard anti-cancer therapy, it is imperative to identify other tumor types expressing beta adrenergic (β-AR) receptors so future preclinical and clinical studies can be directed at the most promising tumor targets. We performed immunohistochemical detection of β1-AR, β2-AR, and β3-AR across 29 of the most common human cancer types (389 tissues total) and 19 matching non-diseased controls (100 tissues total). Our analysis revealed all three β-AR receptors were expressed most strongly in melanoma relative to other cancer types. Other malignancies that revealed relatively higher levels of β-AR receptors were esophagus, pancreas, kidney, and lung cancers. Moreover, particular β-AR receptors exhibited significant overexpression in tumor tissue relative to their matching normal tissue in urogenital/reproductive malignancies including breast, endometrium, ovarian, and urothelial cancer, as well as colon, lung, and thyroid cancer. This study identifies several cancer types expressing the β-AR receptors which should be evaluated in future studies for susceptibility to beta blockade. |
format | Online Article Text |
id | pubmed-5616202 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-56162022017-09-29 Beta-adrenergic receptors are expressed across diverse cancers Rains, Steven L. Amaya, Clarissa N. Bryan, Brad A. Oncoscience Research Paper Based largely on retrospective analyses and a handful of prospective case reports, pharmacological inhibition of the beta adrenergic receptors using beta blockers has shown clinical anti-cancer efficacy in reproductive cancers, as well as angiosarcoma and multiple myeloma. Because of the potential promise of beta blockers as an adjunct to standard anti-cancer therapy, it is imperative to identify other tumor types expressing beta adrenergic (β-AR) receptors so future preclinical and clinical studies can be directed at the most promising tumor targets. We performed immunohistochemical detection of β1-AR, β2-AR, and β3-AR across 29 of the most common human cancer types (389 tissues total) and 19 matching non-diseased controls (100 tissues total). Our analysis revealed all three β-AR receptors were expressed most strongly in melanoma relative to other cancer types. Other malignancies that revealed relatively higher levels of β-AR receptors were esophagus, pancreas, kidney, and lung cancers. Moreover, particular β-AR receptors exhibited significant overexpression in tumor tissue relative to their matching normal tissue in urogenital/reproductive malignancies including breast, endometrium, ovarian, and urothelial cancer, as well as colon, lung, and thyroid cancer. This study identifies several cancer types expressing the β-AR receptors which should be evaluated in future studies for susceptibility to beta blockade. Impact Journals LLC 2017-08-23 /pmc/articles/PMC5616202/ /pubmed/28966942 http://dx.doi.org/10.18632/oncoscience.357 Text en Copyright: © 2017 Rains et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Research Paper Rains, Steven L. Amaya, Clarissa N. Bryan, Brad A. Beta-adrenergic receptors are expressed across diverse cancers |
title | Beta-adrenergic receptors are expressed across diverse cancers |
title_full | Beta-adrenergic receptors are expressed across diverse cancers |
title_fullStr | Beta-adrenergic receptors are expressed across diverse cancers |
title_full_unstemmed | Beta-adrenergic receptors are expressed across diverse cancers |
title_short | Beta-adrenergic receptors are expressed across diverse cancers |
title_sort | beta-adrenergic receptors are expressed across diverse cancers |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5616202/ https://www.ncbi.nlm.nih.gov/pubmed/28966942 http://dx.doi.org/10.18632/oncoscience.357 |
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