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Updated: Dec 21, 2025

Studying Triple Negative Breast Cancer Using Orthotopic Breast Cancer Model
Published on: March 20, 2020
Molecular subtypes and precision treatment of triple-negative breast cancer
Shen Zhao1, Wen-Jia Zuo1, Zhi-Ming Shao1
1Department of Breast Surgery, Fudan University Shanghai Cancer Center, Shanghai 200032, China.
Abstract:
Triple-negative breast cancer (TNBC) is the most aggressive breast cancer subtype. Despite the progress made in precision treatment of cancer patients, targeted treatment is still at its early stage in TNBC, and chemotherapy remains the standard treatment. With the advances in next generation sequencing technology, genomic and transcriptomic analyses have provided deeper insight into the inter-tumoral heterogeneity of TNBC. Much effort has been made to classify TNBCs into different molecular subtypes according to genetic aberrations and expression signatures and to uncover novel treatment targets. In this review, we summarized the current knowledge regarding the molecular classification of TNBC and explore the future paradigm for using molecular classification to guide the development of precision treatment and clinical practice.
Insights
Triple-negative breast cancer (TNBC) is aggressive, lacking targeted therapies. Molecular classification using genomic data offers a path toward precision medicine for TNBC patients.
Area of Science:
- Oncology
- Genomics
- Molecular Biology
Background:
- Triple-negative breast cancer (TNBC) is the most aggressive subtype, with chemotherapy as the primary treatment.
- Targeted therapies for TNBC are limited, despite advances in precision medicine for other cancers.
- Inter-tumoral heterogeneity in TNBC necessitates novel classification strategies.
Purpose of the Study:
- To review current knowledge on TNBC molecular classification.
- To explore how molecular subtypes can guide precision treatment development.
- To discuss the future clinical application of molecular classification in TNBC.
Main Methods:
- Genomic and transcriptomic analyses using next-generation sequencing.
- Review of existing literature on TNBC molecular subtypes.
- Analysis of genetic aberrations and expression signatures.
Main Results:
- TNBC exhibits significant inter-tumoral heterogeneity.
- Molecular classification efforts aim to define distinct TNBC subtypes.
- Identification of potential novel therapeutic targets based on molecular profiles.
Conclusions:
- Molecular classification is crucial for understanding TNBC heterogeneity.
- Developing precision treatments for TNBC requires robust molecular subtyping.
- Future clinical practice may integrate molecular classification for personalized TNBC therapy.
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