Beta-adrenergic blocking drugs in breast cancer: a perspective review

The purpose of this review is to present the preclinical, epidemiological and clinical data relevant to the association between β-blockers and breast cancer progression. Preclinical studies have shown that β-adrenergic receptor (β-AR) signalling can inhibit multiple cellular processes involved in br...

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Main Authors: Thomas I. Barron, Linda Sharp, Kala Visvanathan
Format: Article
Language:English
Published: SAGE Publishing 2012-05-01
Series:Therapeutic Advances in Medical Oncology
Online Access:https://doi.org/10.1177/1758834012439738
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spelling doaj-26a03cde7f194ccc9ab4947fd53379bf2020-11-25T03:34:45ZengSAGE PublishingTherapeutic Advances in Medical Oncology1758-83401758-83592012-05-01410.1177/1758834012439738Beta-adrenergic blocking drugs in breast cancer: a perspective reviewThomas I. BarronLinda SharpKala VisvanathanThe purpose of this review is to present the preclinical, epidemiological and clinical data relevant to the association between β-blockers and breast cancer progression. Preclinical studies have shown that β-adrenergic receptor (β-AR) signalling can inhibit multiple cellular processes involved in breast cancer progression and metastasis, including extracellular matrix invasion, expression of inflammatory and chemotactic cytokines, angiogenesis and tumour immune responses. This has led to the hypothesis that the commonly prescribed class of β-AR antagonist drugs (β-blockers) may favourably impact cancer progression. A number of recent pharmacoepidemiological studies have examined the association between β-blocker exposure and breast cancer progression. The results from these studies have suggested a potential role for targeting the β-AR pathway in breast cancer patients. Larger observational studies are, however, required to confirm these results. Questions regarding the type of β-blocker, predictive biomarkers or tumour characteristics, appropriate treatment paradigms and, most importantly, efficacy must also be answered in randomized clinical studies before β-blockers can be considered a therapeutic option for patients with breast cancer.https://doi.org/10.1177/1758834012439738
collection DOAJ
language English
format Article
sources DOAJ
author Thomas I. Barron
Linda Sharp
Kala Visvanathan
spellingShingle Thomas I. Barron
Linda Sharp
Kala Visvanathan
Beta-adrenergic blocking drugs in breast cancer: a perspective review
Therapeutic Advances in Medical Oncology
author_facet Thomas I. Barron
Linda Sharp
Kala Visvanathan
author_sort Thomas I. Barron
title Beta-adrenergic blocking drugs in breast cancer: a perspective review
title_short Beta-adrenergic blocking drugs in breast cancer: a perspective review
title_full Beta-adrenergic blocking drugs in breast cancer: a perspective review
title_fullStr Beta-adrenergic blocking drugs in breast cancer: a perspective review
title_full_unstemmed Beta-adrenergic blocking drugs in breast cancer: a perspective review
title_sort beta-adrenergic blocking drugs in breast cancer: a perspective review
publisher SAGE Publishing
series Therapeutic Advances in Medical Oncology
issn 1758-8340
1758-8359
publishDate 2012-05-01
description The purpose of this review is to present the preclinical, epidemiological and clinical data relevant to the association between β-blockers and breast cancer progression. Preclinical studies have shown that β-adrenergic receptor (β-AR) signalling can inhibit multiple cellular processes involved in breast cancer progression and metastasis, including extracellular matrix invasion, expression of inflammatory and chemotactic cytokines, angiogenesis and tumour immune responses. This has led to the hypothesis that the commonly prescribed class of β-AR antagonist drugs (β-blockers) may favourably impact cancer progression. A number of recent pharmacoepidemiological studies have examined the association between β-blocker exposure and breast cancer progression. The results from these studies have suggested a potential role for targeting the β-AR pathway in breast cancer patients. Larger observational studies are, however, required to confirm these results. Questions regarding the type of β-blocker, predictive biomarkers or tumour characteristics, appropriate treatment paradigms and, most importantly, efficacy must also be answered in randomized clinical studies before β-blockers can be considered a therapeutic option for patients with breast cancer.
url https://doi.org/10.1177/1758834012439738
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