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Updated: Jun 15, 2026

Isolation and Functional Assessment of Human Breast Cancer Stem Cells from Cell and Tissue Samples
Published on: October 2, 2020
Molecular biology of breast cancer stem cells: potential clinical applications
Nam P Nguyen1, Fabio S Almeida, Alex Chi
1Department of Radiation Oncology, University of Arizona, N. Campbell Ave, Tucson, AZ 85724-5081, USA. NamPhong.Nguyen@yahoo.com
Abstract:
Breast cancer stem cells (CSC) have been postulated recently as responsible for failure of breast cancer treatment. The purpose of this study is to review breast CSCs molecular biology with respect to their mechanism of resistance to conventional therapy, and to develop treatment strategies that may improve survival of breast cancer patients. A literature search has identified in vitro and in vivo studies of breast CSCs. Breast CSCs overexpress breast cancer resistance protein (BCRP) which allows cancer cells to transport actively chemotherapy agents out of the cells. Radioresistance is modulated through activation of Wnt signaling pathway and overexpression of genes coding for glutathione. Lapatinib can selectively target HER-2 positive breast CSCs and improves disease-free survival in these patients. Metformin may target basal type breast CSCs. Parthenolide and oncolytic viruses are promising targeting agents for breast CSCs. Future clinical trials for breast cancer should include anti-cancer stem cells targeting agents in addition to conventional chemotherapy. Hypofractionation radiotherapy may be indicated for residual disease post chemotherapy.
Insights
Breast cancer stem cells (CSCs) resist conventional therapy via mechanisms like BCRP overexpression. Targeting CSCs with agents like lapatinib or metformin may improve breast cancer patient survival.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Stem Cell Research
Background:
- Breast cancer stem cells (CSCs) are implicated in treatment failure.
- Understanding CSC resistance mechanisms is crucial for improving patient outcomes.
Purpose of the Study:
- To review the molecular biology of breast CSCs and their resistance mechanisms.
- To explore novel therapeutic strategies targeting breast CSCs for improved survival.
Main Methods:
- Literature search of in vitro and in vivo studies on breast CSCs.
- Analysis of CSC molecular characteristics, including BCRP overexpression and radioresistance pathways.
Main Results:
- Breast CSCs exhibit resistance through BCRP overexpression, actively exporting chemotherapy agents.
- Wnt signaling pathway activation and glutathione gene overexpression contribute to radioresistance.
- Lapatinib shows efficacy against HER-2 positive breast CSCs, improving disease-free survival.
- Metformin, parthenolide, and oncolytic viruses are potential agents for targeting CSCs.
Conclusions:
- Targeting breast CSCs with novel agents alongside conventional chemotherapy is recommended for future clinical trials.
- Hypofractionation radiotherapy may be beneficial for residual disease post-chemotherapy.
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