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Updated: May 11, 2026

Isolation and Functional Assessment of Human Breast Cancer Stem Cells from Cell and Tissue Samples
Published on: October 2, 2020
Broussoflavonol B restricts growth of ER-negative breast cancer stem-like cells
Mingxi Guo1, Molin Wang, Xintian Zhang
1Department of Medical Microbiology and Immunology, Creighton University Medical School, Criss III, Room 352, 2500 California Plaza, Omaha, NE 68178, USA.
Abstract:
Accumulating experimental and clinical evidence has indicated that tumor-initiating or cancer stem-like cells are a sub-population of tumor cells capable of initiating and driving tumor growth, and cancer stem-like cells are resistant to most current cancer therapies, including chemo- and radiation therapy. More effective targeted-therapeutic approaches are urgently needed to eliminate cancer stem-like cells. Here, we report that broussoflavonol B, a chemical purified from the bark of the Paper Mulberry tree (broussonetia papyrifera), exhibited potent growth inhibitory activity towards estrogen receptor (ER)-negative breast cancer SK-BR-3 cells at sub-micromolar concentrations. Broussoflavonol B more potently inhibited growth and induced differentiation of stem-like SK-BR-3 cells-compared to the anti-estrogen tamoxifen. In addition, broussoflavonol B treatment also reduced the steady, state levels of the Human epidermal growth factor receptor-2 (HER2) and ER-α36, a variant of ER-α. Our results, thus, indicate that broussoflavonol B is a potent growth inhibitor of ER-negative breast cancer stem-like cells and provide a rationale for pre-clinical and clinical evaluation of broussoflavonol B for breast cancer therapy.
Insights
Broussoflavonol B, derived from Paper Mulberry, effectively inhibits estrogen receptor-negative breast cancer stem-like cells. This compound shows promise as a targeted therapy, outperforming tamoxifen in growth inhibition and differentiation induction.
Area of Science:
- Oncology
- Pharmacology
- Natural Products Chemistry
Background:
- Cancer stem-like cells drive tumor growth and therapy resistance.
- Estrogen receptor (ER)-negative breast cancer, particularly HER2-positive subtypes, requires novel therapeutic strategies.
- Targeting cancer stem-like cells is crucial for effective breast cancer treatment.
Purpose of the Study:
- To investigate the anti-cancer effects of broussoflavonol B on ER-negative breast cancer stem-like cells.
- To compare the efficacy of broussoflavonol B with tamoxifen in inhibiting cancer stem-like cell growth and inducing differentiation.
- To explore the molecular targets of broussoflavonol B in breast cancer cells.
Main Methods:
- In vitro cell culture of SK-BR-3 cells, a model for ER-negative breast cancer.
- Treatment with broussoflavonol B and tamoxifen at sub-micromolar concentrations.
- Assessment of cell growth inhibition and differentiation induction.
- Analysis of Human epidermal growth factor receptor-2 (HER2) and ER-α36 protein levels via Western blotting or similar techniques.
Main Results:
- Broussoflavonol B demonstrated potent growth inhibitory activity against ER-negative breast cancer SK-BR-3 cells.
- Broussoflavonol B was more effective than tamoxifen in inhibiting growth and inducing differentiation of stem-like SK-BR-3 cells.
- Treatment with broussoflavonol B led to reduced levels of HER2 and ER-α36.
Conclusions:
- Broussoflavonol B is a potent inhibitor of ER-negative breast cancer stem-like cells.
- Broussoflavonol B exhibits therapeutic potential by targeting key pathways involved in breast cancer stemness and proliferation.
- Further pre-clinical and clinical evaluation of broussoflavonol B is warranted for breast cancer therapy.
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