Abstract
Targeting of estrogen receptor is commonly used as a first-line treatment for hormone-positive breast cancer patients, and is considered as a keystone of systemic cancer therapy. Likewise, HER2-targeted therapy significantly improved the survival of HER2-positive breast cancer patients, indicating that targeted therapy is a powerful therapeutic strategy for breast cancer. However, for triple-negative breast cancer (TNBC), an aggressive breast cancer subtype, there are no clinically approved targeted therapies, and thus, an urgent need to identify potent, highly effective therapeutic targets. In this mini-review, we describe general strategies to inhibit tumor growth by targeted therapies and briefly discuss emerging resistance mechanisms. Particularly, we focus on therapeutic targets for TNBC and discuss combination therapies targeting the epidermal growth factor receptor (EGFR) and associated resistance mechanisms.
| Original language | English GB |
|---|---|
| Pages (from-to) | 657-665 |
| Number of pages | 9 |
| Journal | Biochemical Society Transactions |
| Volume | 48 |
| Issue number | 2 |
| Early online date | 20 Apr 2020 |
| DOIs | |
| State | Published - 29 Apr 2020 |
ASJC Scopus subject areas
- Biochemistry
Fingerprint
Dive into the research topics of 'Targeted therapy and drug resistance in triple-negative breast cancer: the EGFR axis'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver