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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2018-01-01
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Series: | International Journal of Breast Cancer |
Online Access: | http://dx.doi.org/10.1155/2018/7835095 |
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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 |
work_keys_str_mv |
AT troybschedin overcomingtherapeuticresistanceoftriplepositivebreastcancerwithcdk46inhibition AT virginiafborges overcomingtherapeuticresistanceoftriplepositivebreastcancerwithcdk46inhibition AT elenashagisultanova overcomingtherapeuticresistanceoftriplepositivebreastcancerwithcdk46inhibition |
_version_ |
1725912223940870144 |