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Published on: January 18, 2017
Sulforaphane, a dietary component of broccoli/broccoli sprouts, inhibits breast cancer stem cells
Yanyan Li1, Tao Zhang, Hasan Korkaya
1Department of Pharmaceutical Sciences, College of Pharmacy, University of Michigan, Ann Arbor, MI 48109, USA.
Purpose:
The existence of cancer stem cells (CSCs) in breast cancer has profound implications for cancer prevention. In this study, we evaluated sulforaphane, a natural compound derived from broccoli/broccoli sprouts, for its efficacy to inhibit breast CSCs and its potential mechanism.
Experimental Design:
Aldefluor assay and mammosphere formation assay were used to evaluate the effect of sulforaphane on breast CSCs in vitro. A nonobese diabetic/severe combined immunodeficient xenograft model was used to determine whether sulforaphane could target breast CSCs in vivo, as assessed by Aldefluor assay, and tumor growth upon cell reimplantation in secondary mice. The potential mechanism was investigated using Western blotting analysis and beta-catenin reporter assay.
Results:
Sulforaphane (1-5 micromol/L) decreased aldehyde dehydrogenase-positive cell population by 65% to 80% in human breast cancer cells (P < 0.01) and reduced the size and number of primary mammospheres by 8- to 125-fold and 45% to 75% (P < 0.01), respectively. Daily injection with 50 mg/kg sulforaphane for 2 weeks reduced aldehyde dehydrogenase-positive cells by >50% in nonobese diabetic/severe combined immunodeficient xenograft tumors (P = 0.003). Sulforaphane eliminated breast CSCs in vivo, thereby abrogating tumor growth after the reimplantation of primary tumor cells into the secondary mice (P < 0.01). Western blotting analysis and beta-catenin reporter assay showed that sulforaphane downregulated the Wnt/beta-catenin self-renewal pathway.
Conclusions:
Sulforaphane inhibits breast CSCs and downregulates the Wnt/beta-catenin self-renewal pathway. These findings support the use of sulforaphane for the chemoprevention of breast cancer stem cells and warrant further clinical evaluation.
Insights
Sulforaphane, a broccoli compound, effectively inhibits breast cancer stem cells (CSCs) by targeting the Wnt/beta-catenin pathway. This natural agent shows promise for breast cancer prevention and warrants further clinical investigation.
Area of Science:
- Oncology
- Natural Product Chemistry
- Cancer Stem Cell Biology
Background:
- Cancer stem cells (CSCs) are implicated in breast cancer initiation, progression, and treatment resistance.
- Targeting CSCs is crucial for effective breast cancer prevention and therapy.
- Sulforaphane, a natural compound from broccoli, is being investigated for its anti-cancer properties.
Purpose of the Study:
- To evaluate the efficacy of sulforaphane in inhibiting breast CSCs.
- To elucidate the mechanism by which sulforaphane affects breast CSCs.
- To assess sulforaphane's potential for breast cancer chemoprevention.
Main Methods:
- In vitro assays: Aldefluor and mammosphere formation assays to assess CSC activity.
- In vivo xenograft model: Nonobese diabetic/severe combined immunodeficient mice to evaluate sulforaphane's effect on CSCs and tumor growth.
- Mechanism investigation: Western blotting and beta-catenin reporter assay to analyze pathway modulation.
Main Results:
- Sulforaphane significantly reduced aldehyde dehydrogenase-positive CSC populations (65-80%) and mammosphere formation in vitro.
- In vivo, sulforaphane administration decreased CSCs in xenograft tumors and abrogated tumor growth upon secondary implantation.
- Sulforaphane was found to downregulate the Wnt/beta-catenin self-renewal pathway.
Conclusions:
- Sulforaphane demonstrates potent inhibition of breast CSCs both in vitro and in vivo.
- The Wnt/beta-catenin pathway is a key target for sulforaphane's CSC-inhibitory effects.
- Sulforaphane holds potential as a chemopreventive agent against breast cancer stem cells, meriting clinical trials.
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