miR-600 Acts as a Bimodal Switch that Regulates Breast Cancer Stem Cell Fate through WNT Signaling

authors

• El Helou Rita
• Pinna Guillaume
• Cabaud Olivier
• Wicinski Julien
• Bhajun Ricky
• Guyon Laurent
• Rioualen Claire
• Finetti Pascal
• Gros Abigaelle
• Mari Bernard
• Barbry Pascal
• Bertucci François
• Bidaut Ghislain
• Harel-Bellan Annick
• Birnbaum Daniel
• Charafe-Jauffret Emmanuelle
• Ginestier Christophe

abstract

Breast cancer stem cells (bCSCs) have been implicated in tumor progression and therapeutic resistance; however, the molecular mechanisms that define this state are unclear. We have performed two microRNA (miRNA) gain- and loss-of-function screens to identify miRNAs that regulate the choice between bCSC self-renewal and differentiation. We find that micro-RNA (miR)-600 silencing results in bCSC expansion, while its overexpression reduces bCSC self-renewal, leading to decreased in vivo tumorigenicity. miR-600 targets stearoyl desaturase 1 (SCD1), an enzyme required to produce active, lipid-modified WNT proteins. In the absence of miR-600, WNT signaling is active and promotes self-renewal, whereas overexpression of miR-600 inhibits the production of active WNT and promotes bCSC differentiation. In a series of 120 breast tumors, we found that a low level of miR-600 is correlated with active WNT signaling and a poor prognosis. These findings highlight a miR-600-centered signaling network that governs bCSC-fate decisions and influences tumor progression

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