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.

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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