Abstract Title:

Quercetin suppresses breast cancer stem cells (CD44+/CD24-) by inhibiting the PI3K/Akt/mTOR-signaling pathway.

Abstract Source:

Life Sci. 2018 Jan 16. Epub 2018 Jan 16. PMID: 29355544

Abstract Author(s):

Xiuli Li, Na Zhou, Jin Wang, Zhijie Liu, Xiaohui Wang, Qin Zhang, Qingyan Liu, Lifeng Gao, Rong Wang

Article Affiliation:

Xiuli Li


AIMS: Cancer stem cells (CSCs) are considered the prime source of cancer recurrence, metastasis, and progression and represent important targets for developing novel anticancer agents and therapeutic strategies. The aim of this study was to investigate the effect of treating breast CSCs with the anticancer flavonoid, quercetin.

MAIN METHODS: We examined changes in the cluster of differentiation CD44+/CD24-CSC population and behavior using the breast cancer cell line MCF-7.

KEY FINDINGS: Our results indicated that cell viability, clone formation, mammosphere generation, and nude mice tumor metastasis were inhibited in the CD44+/CD24- population and that MCF-7 cells exhibited G1-phase arrest after quercetin treatment. Additionally, CyclinD1 and B cell lymphoma-2 expression were suppressed and Bcl-2-like protein-4 expression was enhanced after quercetin treatment. We also observed that estrogen receptorα and phosphatidylinositol-3-kinase (PI3K)/Akt/mammalian target of rapamycin (mTOR) signaling were downregulated concurrently with the inhibition of CD44+/CD24- viability and clone formation. Our findings suggested that quercetin treatment promoted weaker malignant activity associated with CSCs relative to that observed in normal cancer cells through its inhibition of the PI3K/Akt/mTOR-signaling pathway.

SIGNIFICANCE: These results indicated that CSCs are potential therapeutic targets for quercetin treatment of breast cancer.

Study Type : In Vitro Study

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Sayer Ji
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