Open Access
Open access
Oncotarget, volume 9, issue 45, pages 27773-27788

Activating HER3 mutations in breast cancer

MISHRA ROSALIN 1
Alanazi Samar 1
Yuan Long 1
Solomon Thomas C. 1
Thaker Tarjani M. 2
Jura Natalia 2
Garrett Joan T. 1
1
 
James L. Winkle College of Pharmacy, University of Ohio, Cincinnati, Ohio, USA
2
 
Department of Cellular and Molecular Pharmacology, Cardiovascular Research Institute, University of California, San Francisco, California, USA
Publication typeJournal Article
Publication date2018-06-11
Journal: Oncotarget
Quartile SCImago
Q2
Quartile WOS
Impact factor
ISSN19492553
Oncology
Abstract
Recent studies have highlighted a role of HER3 in ER and HER2-driven breast cancers. We sought to investigate the role of patient-derived HER3 mutations in ER+ and HER2+ breast cancer cells using ectopic expression of HER3 mutants. We found that HER3T355I mutant is activating with increased cell proliferation in ER+ T47D and MCF-7 breast cancer cells lacking HER2 over-expression. Immunoblotting and receptor tyrosine kinase array results indicated that T47D and MCF-7 cells expressing HER3T355I had increased p-HER4 and p-HER1 expression. Our data showed that HER3T355I induced cell proliferation is via HER4/HER1-dependent ERK1/2 and cyclinD1 mediated pathways in ER+ cells. ERα expression is upregulated in ER+ cells expressing HER3T355I mutant. We noted crosstalk between ERα and HER3 in T47D cells. Several HER3 mutants (F94L, G284R, D297Y, T355I, and E1261A) acquired a gain-of-function phenotype in MCF10AHER2 cells and were resistant to lapatinib. These mutants increased HER2-HER3 heterodimerization. Knocking down HER3 from ovarian and colorectal cancers with endogenous HER3 mutations abrogated cancer cell proliferation. Overall, this study provides the first systematic assessment of how mutations in HER3 affect response of ER+ and HER2+ breast cancers to clinically relevant inhibitors and finds that HER3 mutations can be activating independent of HER2 over-expression.

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GOST |
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GOST Copy
MISHRA R. et al. Activating HER3 mutations in breast cancer // Oncotarget. 2018. Vol. 9. No. 45. pp. 27773-27788.
GOST all authors (up to 50) Copy
MISHRA R., Alanazi S., Yuan L., Solomon T. C., Thaker T. M., Jura N., Garrett J. T. Activating HER3 mutations in breast cancer // Oncotarget. 2018. Vol. 9. No. 45. pp. 27773-27788.
RIS |
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RIS Copy
TY - JOUR
DO - 10.18632/oncotarget.25576
UR - https://doi.org/10.18632%2Foncotarget.25576
TI - Activating HER3 mutations in breast cancer
T2 - Oncotarget
AU - MISHRA, ROSALIN
AU - Alanazi, Samar
AU - Yuan, Long
AU - Solomon, Thomas C.
AU - Thaker, Tarjani M.
AU - Jura, Natalia
AU - Garrett, Joan T.
PY - 2018
DA - 2018/06/11 00:00:00
PB - Impact Journals
SP - 27773-27788
IS - 45
VL - 9
PMID - 29963236
SN - 1949-2553
ER -
BibTex |
Cite this
BibTex Copy
@article{2018_MISHRA,
author = {ROSALIN MISHRA and Samar Alanazi and Long Yuan and Thomas C. Solomon and Tarjani M. Thaker and Natalia Jura and Joan T. Garrett},
title = {Activating HER3 mutations in breast cancer},
journal = {Oncotarget},
year = {2018},
volume = {9},
publisher = {Impact Journals},
month = {jun},
url = {https://doi.org/10.18632%2Foncotarget.25576},
number = {45},
pages = {27773--27788},
doi = {10.18632/oncotarget.25576}
}
MLA
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MLA Copy
MISHRA, ROSALIN, et al. “Activating HER3 mutations in breast cancer.” Oncotarget, vol. 9, no. 45, Jun. 2018, pp. 27773-27788. https://doi.org/10.18632%2Foncotarget.25576.
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