Overcoming Therapeutic Resistance of Triple Positive Breast Cancer with CDK4/6 Inhibition

Triple positive breast cancers overexpress both the human epidermal growth factor receptor 2 (HER2) oncogene and the hormonal receptors (HR) to estrogen and progesterone. These cancers represent a unique therapeutic challenge because of a bidirectional cross-talk between the estrogen receptor alpha...

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Main Authors: Troy B. Schedin, Virginia F. Borges, Elena Shagisultanova
Format: Article
Language:English
Published: Hindawi Limited 2018-01-01
Series:International Journal of Breast Cancer
Online Access:http://dx.doi.org/10.1155/2018/7835095
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spelling doaj-2887162eaf5b4c3999d19a13c739b2cd2020-11-24T21:43:45ZengHindawi LimitedInternational Journal of Breast Cancer2090-31702090-31892018-01-01201810.1155/2018/78350957835095Overcoming Therapeutic Resistance of Triple Positive Breast Cancer with CDK4/6 InhibitionTroy B. Schedin0Virginia F. Borges1Elena Shagisultanova2Young Women’s Breast Cancer Translational Program, University of Colorado Denver, 13001 E 17th Pl, Aurora, CO 80045, USAYoung Women’s Breast Cancer Translational Program, University of Colorado Denver, 13001 E 17th Pl, Aurora, CO 80045, USAYoung Women’s Breast Cancer Translational Program, University of Colorado Denver, 13001 E 17th Pl, Aurora, CO 80045, USATriple positive breast cancers overexpress both the human epidermal growth factor receptor 2 (HER2) oncogene and the hormonal receptors (HR) to estrogen and progesterone. These cancers represent a unique therapeutic challenge because of a bidirectional cross-talk between the estrogen receptor alpha (ERα) and HER2 pathways leading to tumor progression and resistance to targeted therapy. Attempts to combine standard of care HER2-targeted drugs with antihormonal agents for the treatment of HR+/HER2+ breast cancer yielded encouraging results in preclinical experiments but did improve overall survival in clinical trial. In this review, we dissect multiple mechanisms of therapeutic resistance typical of HR+/HER2+ breast cancer, summarize prior clinical trials of targeted agents, and describe novel rational drug combinations that include antihormonal agents, HER2-targeted drugs, and CDK4/6 inhibitors for treatment of the HR+/HER2+ breast cancer subtype.http://dx.doi.org/10.1155/2018/7835095
collection DOAJ
language English
format Article
sources DOAJ
author Troy B. Schedin
Virginia F. Borges
Elena Shagisultanova
spellingShingle Troy B. Schedin
Virginia F. Borges
Elena Shagisultanova
Overcoming Therapeutic Resistance of Triple Positive Breast Cancer with CDK4/6 Inhibition
International Journal of Breast Cancer
author_facet Troy B. Schedin
Virginia F. Borges
Elena Shagisultanova
author_sort Troy B. Schedin
title Overcoming Therapeutic Resistance of Triple Positive Breast Cancer with CDK4/6 Inhibition
title_short Overcoming Therapeutic Resistance of Triple Positive Breast Cancer with CDK4/6 Inhibition
title_full Overcoming Therapeutic Resistance of Triple Positive Breast Cancer with CDK4/6 Inhibition
title_fullStr Overcoming Therapeutic Resistance of Triple Positive Breast Cancer with CDK4/6 Inhibition
title_full_unstemmed Overcoming Therapeutic Resistance of Triple Positive Breast Cancer with CDK4/6 Inhibition
title_sort overcoming therapeutic resistance of triple positive breast cancer with cdk4/6 inhibition
publisher Hindawi Limited
series International Journal of Breast Cancer
issn 2090-3170
2090-3189
publishDate 2018-01-01
description Triple positive breast cancers overexpress both the human epidermal growth factor receptor 2 (HER2) oncogene and the hormonal receptors (HR) to estrogen and progesterone. These cancers represent a unique therapeutic challenge because of a bidirectional cross-talk between the estrogen receptor alpha (ERα) and HER2 pathways leading to tumor progression and resistance to targeted therapy. Attempts to combine standard of care HER2-targeted drugs with antihormonal agents for the treatment of HR+/HER2+ breast cancer yielded encouraging results in preclinical experiments but did improve overall survival in clinical trial. In this review, we dissect multiple mechanisms of therapeutic resistance typical of HR+/HER2+ breast cancer, summarize prior clinical trials of targeted agents, and describe novel rational drug combinations that include antihormonal agents, HER2-targeted drugs, and CDK4/6 inhibitors for treatment of the HR+/HER2+ breast cancer subtype.
url http://dx.doi.org/10.1155/2018/7835095
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AT elenashagisultanova overcomingtherapeuticresistanceoftriplepositivebreastcancerwithcdk46inhibition
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