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Updated: Jun 21, 2026

Studying Triple Negative Breast Cancer Using Orthotopic Breast Cancer Model
Published on: March 20, 2020
Triple-negative breast cancer: novel therapies and new directions
Sumanta Kumar Pal1, Joanne Mortimer
1Division of Genitourinary Malignancies, Department of Medical Oncology & Experimental Therapeutics, City of Hope Comprehensive Cancer Center, Duarte, CA 91010, USA. spal@coh.org
Abstract:
Triple-negative breast cancer (TNBC) accounts for approximately 15% of breast cancer diagnoses, and exhibits substantial overlap with basal-type and BRCA1-positive breast cancer. In recent years, a greater understanding of the biology of this disease has led to the development of numerous and varied therapeutic approaches. Neoadjuvant trials using conventional cytotoxic agents such as cisplatin have demonstrated TNBC to be a relatively chemo-sensitive disease. In the current review, focus is directed towards novel targeted strategies for TNBC. Recent trials have shown the poly(ADP-ribosyl)ation polymerase (PARP) inhibitors BSI-201 and olaparib to be highly effective in TNBC and BRCA1/2-positive disease, respectively. Efforts to assess the role of antiangiogenic agents such as bevacizumab and sunitinib in TNBC are ongoing. Finally, preclinical studies provide a signal of potential activity with use of heat shock protein 90 (Hsp90) and Src inhibitors in this breast cancer subtype.
Insights
Novel targeted therapies show promise for triple-negative breast cancer (TNBC). Poly(ADP-ribosyl)ation polymerase (PARP) inhibitors and other agents are being investigated for improved treatment outcomes in this aggressive subtype.
Area of Science:
- Oncology
- Translational Medicine
- Genetics
Background:
- Triple-negative breast cancer (TNBC) represents about 15% of breast cancer cases.
- TNBC shares characteristics with basal-type and BRCA1-positive breast cancer.
- Conventional cytotoxic agents show TNBC is chemo-sensitive.
Purpose of the Study:
- To review novel targeted therapeutic strategies for triple-negative breast cancer.
- To highlight recent advancements and ongoing research in TNBC treatment.
Main Methods:
- Review of recent clinical trials and preclinical studies.
- Focus on targeted agents beyond conventional chemotherapy.
Main Results:
- Poly(ADP-ribosyl)ation polymerase (PARP) inhibitors (BSI-201, olaparib) show high efficacy in TNBC and BRCA1/2-positive disease.
- Antiangiogenic agents (bevacizumab, sunitinib) are under investigation.
- Preclinical data suggest potential activity for heat shock protein 90 (Hsp90) and Src inhibitors.
Conclusions:
- Targeted therapies, including PARP inhibitors, offer new avenues for TNBC treatment.
- Ongoing research into antiangiogenic, Hsp90, and Src inhibitors may yield future therapeutic options.
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