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Updated: Jul 17, 2025

Studying Triple Negative Breast Cancer Using Orthotopic Breast Cancer Model
Published on: March 20, 2020
Recent advances in targeted strategies for triple-negative breast cancer
Shuangli Zhu1, Yuze Wu1, Bin Song2
1Department of Oncology, Tongji Hospital of Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
Abstract:
Triple-negative breast cancer (TNBC), a highly aggressive subtype of breast cancer, negatively expresses estrogen receptor, progesterone receptor, and the human epidermal growth factor receptor 2 (HER2). Although chemotherapy is the main form of treatment for patients with TNBC, the effectiveness of chemotherapy for TNBC is still limited. The search for more effective therapies is urgent. Multiple targeted therapeutic strategies have emerged according to the specific molecules and signaling pathways expressed in TNBC. These include PI3K/AKT/mTOR inhibitors, epidermal growth factor receptor inhibitors, Notch inhibitors, poly ADP-ribose polymerase inhibitors, and antibody-drug conjugates. Moreover, immune checkpoint inhibitors, for example, pembrolizumab, atezolizumab, and durvalumab, are widely explored in the clinic. We summarize recent advances in targeted therapy and immunotherapy in TNBC, with the aim of serving as a reference for the development of individualized treatment of patients with TNBC in the future.
Insights
Triple-negative breast cancer (TNBC) treatments are limited. New targeted therapies and immunotherapies show promise for improving outcomes in this aggressive cancer subtype.
Area of Science:
- Oncology
- Medical Research
Background:
- Triple-negative breast cancer (TNBC) is an aggressive breast cancer subtype lacking estrogen receptor, progesterone receptor, and HER2 expression.
- Current chemotherapy options for TNBC have limited effectiveness, necessitating urgent development of novel therapeutic strategies.
Purpose of the Study:
- To summarize recent advances in targeted therapy and immunotherapy for TNBC.
- To provide a reference for future development of individualized treatment approaches for TNBC patients.
Main Methods:
- Review of emerging targeted therapeutic strategies including PI3K/AKT/mTOR inhibitors, EGFR inhibitors, Notch inhibitors, PARP inhibitors, and antibody-drug conjugates.
- Exploration of immune checkpoint inhibitors (e.g., pembrolizumab, atezolizumab, durvalumab) in clinical settings for TNBC.
Main Results:
- Multiple targeted therapies are being developed based on specific TNBC molecular pathways.
- Immunotherapies, particularly immune checkpoint inhibitors, are under extensive clinical investigation for TNBC treatment.
Conclusions:
- Significant progress has been made in developing targeted therapies and immunotherapies for TNBC.
- These advancements offer potential for more personalized and effective treatment strategies for patients with triple-negative breast cancer.
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