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β‐Adrenergic signaling in skin cancer

Activation of the sympathetic nervous system releases catecholamines that can interact with β‐adrenergic receptors on tumor cells. Preclinical models have shown that the signaling processes initiated by activation of β‐adrenergic receptors increase tumorigenesis, stimulate cell proliferation, and in...

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Autores principales: Batalla‐Covello, Jennifer, Ali, Shahrukh, Xie, Tongxin, Amit, Moran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8984090/
https://www.ncbi.nlm.nih.gov/pubmed/35415461
http://dx.doi.org/10.1096/fba.2021-00097
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author Batalla‐Covello, Jennifer
Ali, Shahrukh
Xie, Tongxin
Amit, Moran
author_facet Batalla‐Covello, Jennifer
Ali, Shahrukh
Xie, Tongxin
Amit, Moran
author_sort Batalla‐Covello, Jennifer
collection PubMed
description Activation of the sympathetic nervous system releases catecholamines that can interact with β‐adrenergic receptors on tumor cells. Preclinical models have shown that the signaling processes initiated by activation of β‐adrenergic receptors increase tumorigenesis, stimulate cell proliferation, and inhibit apoptosis. Indeed, preclinical studies have also shown that β‐adrenergic blockade can decrease tumor burden. Researchers have been studying the effects of β‐adrenergic receptor blockers on tumor cells and how they may slow the progression of melanoma, basal cell carcinoma, and squamous cell carcinoma. Moreover, clinical data have shown improved prognosis in patients with skin cancer who take β‐blockers. This review discusses the mechanisms of β‐adrenergic signaling in cancer and immune cells, details preclinical models of sympathetic blockade, and considers clinical evidence of the effects of β‐adrenergic blockade in skin cancers.
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spelling pubmed-89840902022-04-11 β‐Adrenergic signaling in skin cancer Batalla‐Covello, Jennifer Ali, Shahrukh Xie, Tongxin Amit, Moran FASEB Bioadv Review Activation of the sympathetic nervous system releases catecholamines that can interact with β‐adrenergic receptors on tumor cells. Preclinical models have shown that the signaling processes initiated by activation of β‐adrenergic receptors increase tumorigenesis, stimulate cell proliferation, and inhibit apoptosis. Indeed, preclinical studies have also shown that β‐adrenergic blockade can decrease tumor burden. Researchers have been studying the effects of β‐adrenergic receptor blockers on tumor cells and how they may slow the progression of melanoma, basal cell carcinoma, and squamous cell carcinoma. Moreover, clinical data have shown improved prognosis in patients with skin cancer who take β‐blockers. This review discusses the mechanisms of β‐adrenergic signaling in cancer and immune cells, details preclinical models of sympathetic blockade, and considers clinical evidence of the effects of β‐adrenergic blockade in skin cancers. John Wiley and Sons Inc. 2022-01-06 /pmc/articles/PMC8984090/ /pubmed/35415461 http://dx.doi.org/10.1096/fba.2021-00097 Text en © 2021 The Authors. FASEB BioAdvances published by Wiley Periodicals LLC on behalf of The Federation of American Societies for Experimental Biology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Review
Batalla‐Covello, Jennifer
Ali, Shahrukh
Xie, Tongxin
Amit, Moran
β‐Adrenergic signaling in skin cancer
title β‐Adrenergic signaling in skin cancer
title_full β‐Adrenergic signaling in skin cancer
title_fullStr β‐Adrenergic signaling in skin cancer
title_full_unstemmed β‐Adrenergic signaling in skin cancer
title_short β‐Adrenergic signaling in skin cancer
title_sort β‐adrenergic signaling in skin cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8984090/
https://www.ncbi.nlm.nih.gov/pubmed/35415461
http://dx.doi.org/10.1096/fba.2021-00097
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