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Updated: Jul 2, 2025

Studying Triple Negative Breast Cancer Using Orthotopic Breast Cancer Model
Published on: March 20, 2020
Targeting Receptor Tyrosine Kinases as a Novel Strategy for the Treatment of Triple-Negative Breast Cancer
Sara K Jaradat1, Nehad M Ayoub1, Ahmed H Al Sharie2
1Department of Clinical Pharmacy, Faculty of Pharmacy, Jordan University of Science and Technology (JUST), Irbid, Jordan.
Abstract:
Triple-negative breast cancer (TNBC) comprises a group of aggressive and heterogeneous breast carcinoma. Chemotherapy is the mainstay for the treatment of triple-negative tumors. Nevertheless, the success of chemotherapeutic treatments is limited by their toxicity and development of acquired resistance leading to therapeutic failure and tumor relapse. Hence, there is an urgent need to explore novel targeted therapies for TNBC. Receptor tyrosine kinases (RTKs) are a family of transmembrane receptors that are key regulators of intracellular signaling pathways controlling cell proliferation, differentiation, survival, and motility. Aberrant activity and/or expression of several types of RTKs have been strongly connected to tumorigenesis. RTKs are frequently overexpressed and/or deregulated in triple-negative breast tumors and are further associated with tumor progression and reduced survival in patients. Therefore, targeting RTKs could be an appealing therapeutic strategy for the treatment of TNBC. This review summarizes the current evidence regarding the antitumor activity of RTK inhibitors in preclinical models of TNBC. The review also provides insights into the clinical trials evaluating the use of RTK inhibitors for the treatment of patients with TNBC.
Insights
Targeting receptor tyrosine kinases (RTKs) offers a promising avenue for treating aggressive triple-negative breast cancer (TNBC). This review explores RTK inhibitors
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Triple-negative breast cancer (TNBC) is an aggressive, heterogeneous cancer with limited treatment options.
- Current chemotherapy for TNBC faces challenges due to toxicity and acquired resistance, necessitating novel therapeutic strategies.
- Receptor tyrosine kinases (RTKs) play crucial roles in cell signaling and are often dysregulated in TNBC, correlating with tumor progression and poor patient outcomes.
Purpose of the Study:
- To review the antitumor activity of RTK inhibitors in preclinical TNBC models.
- To provide insights into ongoing clinical trials evaluating RTK inhibitors for TNBC treatment.
Main Methods:
- Literature review of preclinical studies on RTK inhibitors in TNBC.
- Analysis of clinical trial data for RTK inhibitors in TNBC patients.
Main Results:
- RTK overexpression and deregulation are common in TNBC, linked to adverse prognostic factors.
- Preclinical data suggest significant antitumor effects of various RTK inhibitors against TNBC models.
- Clinical trials are investigating the efficacy and safety of RTK inhibitors in TNBC patients.
Conclusions:
- Targeting RTKs represents a rational and potentially effective therapeutic strategy for TNBC.
- Further research and clinical evaluation of RTK inhibitors are warranted to improve TNBC patient outcomes.
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