Targeting the EphB4 receptor tyrosine kinase sensitizes HER2-positive breast cancer cells to Lapatinib
- PMID: 32006616
- DOI: 10.1016/j.canlet.2020.01.032
Targeting the EphB4 receptor tyrosine kinase sensitizes HER2-positive breast cancer cells to Lapatinib
Abstract
Clinical data analysis reveals that the expression of the EphB4 receptor tyrosine kinase is significantly elevated in HER2-positive breast cancer and high levels of EphB4 strongly correlate with poor disease prognosis. However, the impact of EphB4 activation on HER2-positive breast cancer cells and the potential of EphB4 as a therapeutic target remain to be explored. Here, we show that EphB4 overexpression confers gain-of-function activities to HER2-positive breast cancer cells, rendering resistance to a HER2/EGFR inhibitor Lapatinib. Furthermore, using integrated transcriptomic and tyrosine phosphoproteomic analyses, followed by biochemical confirmation, we establish that EphB4 activation engages the SHP2/GAB1-MEK signaling cascade and downstream c-MYC activation, and thereby limits the overall drug responses to Lapatinib. Finally, we demonstrate that, in HER2-positive breast tumors, inhibition of EphB4 combined with Lapatinib is more effective than either alone. These findings provide new insights into the signaling networks dictating therapeutic response to Lapatinib as well as a rationale for co-targeting EphB4 in HER2-positive breast cancer.
Keywords: Breast cancer; Drug response; EphB4; HER2; Lapatinib.
Copyright © 2020 The Authors. Published by Elsevier B.V. All rights reserved.
Conflict of interest statement
Declaration of competing interest The authors declare that they have no conflict of interest.
Similar articles
-
A novel treatment strategy for lapatinib resistance in a subset of HER2-amplified gastric cancer.BMC Cancer. 2021 Aug 16;21(1):923. doi: 10.1186/s12885-021-08283-9. BMC Cancer. 2021. PMID: 34399705 Free PMC article.
-
Novel Hsp90 inhibitor FW-04-806 displays potent antitumor effects in HER2-positive breast cancer cells as a single agent or in combination with lapatinib.Cancer Lett. 2015 Jan 28;356(2 Pt B):862-71. doi: 10.1016/j.canlet.2014.10.040. Epub 2014 Nov 4. Cancer Lett. 2015. PMID: 25449780
-
CDK12 inhibition enhances sensitivity of HER2+ breast cancers to HER2-tyrosine kinase inhibitor via suppressing PI3K/AKT.Eur J Cancer. 2021 Mar;145:92-108. doi: 10.1016/j.ejca.2020.11.045. Epub 2021 Jan 9. Eur J Cancer. 2021. PMID: 33429148
-
Mechanisms of lapatinib resistance in HER2-driven breast cancer.Cancer Treat Rev. 2015 Dec;41(10):877-83. doi: 10.1016/j.ctrv.2015.08.001. Epub 2015 Aug 8. Cancer Treat Rev. 2015. PMID: 26276735 Review.
-
Lapatinib.Recent Results Cancer Res. 2018;211:19-44. doi: 10.1007/978-3-319-91442-8_2. Recent Results Cancer Res. 2018. PMID: 30069757 Review.
Cited by
-
Homoharringtonine suppresses tumor proliferation and migration by regulating EphB4-mediated β-catenin loss in hepatocellular carcinoma.Cell Death Dis. 2020 Aug 14;11(8):632. doi: 10.1038/s41419-020-02902-2. Cell Death Dis. 2020. PMID: 32801343 Free PMC article.
-
The role of EphA7 in different tumors.Clin Transl Oncol. 2022 Jul;24(7):1274-1289. doi: 10.1007/s12094-022-02783-1. Epub 2022 Feb 2. Clin Transl Oncol. 2022. PMID: 35112312 Review.
-
Targeted dual degradation of HER2 and EGFR obliterates oncogenic signaling, overcomes therapy resistance, and inhibits metastatic lesions in HER2-positive breast cancer models.Drug Resist Updat. 2024 May;74:101078. doi: 10.1016/j.drup.2024.101078. Epub 2024 Mar 13. Drug Resist Updat. 2024. PMID: 38503142
-
Preclinical and Basic Research Strategies for Overcoming Resistance to Targeted Therapies in HER2-Positive Breast Cancer.Cancers (Basel). 2023 Apr 30;15(9):2568. doi: 10.3390/cancers15092568. Cancers (Basel). 2023. PMID: 37174034 Free PMC article. Review.
-
Tyrosine Kinase Inhibitors in the Combination Therapy of HER2 Positive Breast Cancer.Technol Cancer Res Treat. 2020 Jan-Dec;19:1533033820962140. doi: 10.1177/1533033820962140. Technol Cancer Res Treat. 2020. PMID: 33034269 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials
Miscellaneous