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Updated: Oct 13, 2025

Studying Triple Negative Breast Cancer Using Orthotopic Breast Cancer Model
Published on: March 20, 2020
Targeted Therapeutic Strategies for Triple-Negative Breast Cancer
Ying Li1,2, Zhijun Zhan1,2, Xuemin Yin1,2
1Key Laboratory of Model Animals and Stem Cell Biology in Hunan Province, Department of Pathophysiology, Hunan Normal University School of Medicine, Changsha, China.
Abstract:
Triple-negative breast cancer (TNBC) is the most aggressive subtype of breast cancer, which is characterized by the absence of estrogen receptor (ER) and progesterone receptor (PR) expression and the absence of human epidermal growth factor receptor 2 (HER2) expression/amplification. Conventional chemotherapy is the mainstay of systemic treatment for TNBC. However, lack of molecular targeted therapies and poor prognosis of TNBC patients have prompted a great effort to discover effective targets for improving the clinical outcomes. For now, poly (ADP-ribose) polymerase (PARP) inhibitors (PARPi's) and immune checkpoint inhibitors have been approved for the treatment of TNBC. Moreover, agents that target signal transduction, angiogenesis, epigenetic modifications, and cell cycle are under active preclinical or clinical investigations. In this review, we highlight the current major developments in targeted therapies of TNBC, with some descriptions about their (dis)advantages and future perspectives.
Insights
Triple-negative breast cancer (TNBC) treatment is advancing with targeted therapies. Approved options include poly (ADP-ribose) polymerase inhibitors and immune checkpoint inhibitors, offering new hope for patients.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Triple-negative breast cancer (TNBC) is an aggressive subtype lacking ER, PR, and HER2 expression.
- Conventional chemotherapy is the primary treatment, but TNBC has a poor prognosis.
- There is a critical need for effective molecular targeted therapies for TNBC.
Purpose of the Study:
- To review current major developments in targeted therapies for TNBC.
- To discuss the advantages and disadvantages of these emerging treatments.
- To provide insights into future perspectives for TNBC targeted therapy.
Main Methods:
- Literature review of preclinical and clinical investigations.
- Analysis of approved and investigational targeted agents.
- Synthesis of information on signal transduction, angiogenesis, epigenetic modifications, and cell cycle targets.
Main Results:
- Poly (ADP-ribose) polymerase (PARP) inhibitors are approved for TNBC treatment.
- Immune checkpoint inhibitors have also been approved for TNBC.
- Various agents targeting signal transduction, angiogenesis, epigenetics, and cell cycle are under investigation.
Conclusions:
- Targeted therapies represent a significant advancement in TNBC treatment.
- PARP inhibitors and immune checkpoint inhibitors offer new therapeutic avenues.
- Ongoing research into novel targets holds promise for improving clinical outcomes in TNBC.
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