4.2 Article

Silibinin exhibits anti- tumor effects in a breast cancer stem cell model by targeting stemness and induction of differentiation and apoptosis

Journal

BIOIMPACTS
Volume -, Issue -, Pages -

Publisher

TABRIZ UNIV MEDICAL SCIENCES & HEALTH SERVICES
DOI: 10.34172/bi.2022.23336

Keywords

Breast cancer stem cells; Silibinin; Mammospheres; Epithelial to mesenchymal; transition

Funding

  1. Iran National Science Foundation [90003728]
  2. Iranian Council of Stem Cell Research and Technology [REP191]

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This study found that silibinin could target breast cancer stem cells, reducing tumor formation and metastasis. It may be a potential adjuvant for the treatment of breast cancer.
Introduction: Malignant breast cancer (BC) frequently contains a rare population of cells called cancer stem cells which underlie tumor relapse and metastasis, and targeting these cells may improve treatment options and outcomes for patients with BC. The aim of the present study was to determine the effect of silibinin on the selfrenewal capacity, tumorgenicity, and metastatic potential of mammospheres. Methods: The effect of silibinin on viability and proliferation of MCF-7, MDA-MB-231 mammospheres, and MDA-MB-468 cell aggregation was determined after 72-120 hours of treatment. Colony and sphere formation ability, and the expression of stemness, differentiation, and epithelial-mesenchymal-transition (EMT)-associated genes were assessed by reverse transcription-quantitative polymerase chain reaction (qRT-PCR) in mammospheres treated with an IC 50 dose of silibinin. Additionally, the antitumor capacity of silibinin was assessed in vivo, in mice. Results: The results of the present study showed that silibinin decreased the viability of all mammospheres derived from MCF-7, MDA-MB-231, and MDA-MB-468 cell aggregation in a dose-dependent manner. Colony and sphere-forming ability, as well as the expression of genes associated with EMT were reduced in mammospheres treated with silibinin. Additionally, the expression of genes associated with stemness and metastasis was also decreased and the expression of genes associated with differentiation were increased. Intra-tumoral injection of 2 mg/kg silibinin decreased tumor volumes in mice by 2.8 fold. Conclusion: The present study demonstrated that silibinin may have exerted its anti-tumor effects in BC by targeting the BC stem cells, reducing the tumorgenicity and metastasis. Therefore, silibinin may be a potential adjuvant for treatment of BC.

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