Stratification of Tamoxifen Synergistic Combinations for the Treatment of ER+ Breast Cancer

Author:

Zboril Emily K.12,Grible Jacqueline M.1,Boyd David C.13,Hairr Nicole S.1ORCID,Leftwich Tess J.1,Esquivel Madelyn F.1ORCID,Duong Alex K.1ORCID,Turner Scott A.1,Ferreira-Gonzalez Andrea1,Olex Amy L.4ORCID,Sartorius Carol A.5,Dozmorov Mikhail G.6ORCID,Harrell J. Chuck178ORCID

Affiliation:

1. Department of Pathology, Virginia Commonwealth University, Richmond, VA 23298, USA

2. Department of Biochemistry and Molecular Biology, Virginia Commonwealth University, Richmond, VA 23298, USA

3. Integrative Life Sciences Program, Virginia Commonwealth University, Richmond, VA 23298, USA

4. C. Kenneth and Dianne Wright Center for Clinical and Translational Research, Virginia Commonwealth University, Richmond, VA 23298, USA

5. Department of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA

6. Department of Biostatistics, Virginia Commonwealth University, Richmond, VA 23298, USA

7. Massey Cancer Center, Virginia Commonwealth University, Richmond, VA 23298, USA

8. Center for Pharmaceutical Engineering, Virginia Commonwealth University, Richmond, VA 23298, USA

Abstract

Breast cancer alone accounts for the majority of cancer deaths among women, with the most commonly diagnosed subtype being estrogen receptor positive (ER+). Survival has greatly improved for patients with ER+ breast cancer, due in part to the development of antiestrogen compounds, such as tamoxifen. While treatment of the primary disease is often successful, as many as 30% of patients will experience recurrence and metastasis, mainly due to developed endocrine therapy resistance. In this study, we discovered two tamoxifen combination therapies, with simeprevir and VX-680, that reduce the tumor burden in animal models of ER+ breast cancer more than either compound or tamoxifen alone. Additionally, these tamoxifen combinations reduced the expression of HER2, a hallmark of tamoxifen treatment, which can facilitate acquisition of a treatment-resistant phenotype. These combinations could provide clinical benefit by potentiating tamoxifen treatment in ER+ breast cancer.

Funder

National Institutes of Health/National Cancer Institute

Susan G. Komen Foundation

Massey Cancer Center

VCU Health under the Value and Efficiency Teaching and Research (VETAR) program

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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