
Faculty, Staff and Student Publications
Publication Date
4-1-2022
Journal
FASEB BioAdvances
Abstract
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.
Keywords
adrenergic system, basal cell carcinoma, melanoma, skin cancer, squamous cell carcinoma, sympathetic nervous system, β‐adrenergic, β‐adrenergic signaling, β‐blockers
DOI
10.1096/fba.2021-00097
PMID
35415461
PMCID
PMC8984090
PubMedCentral® Posted Date
1-6-2022
PubMedCentral® Full Text Version
Post-print
Published Open-Access
yes
Included in
Bioinformatics Commons, Biomedical Informatics Commons, Medical Sciences Commons, Oncology Commons