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MicroRNA93 regulates proliferation and differentiation of normal and malignant breast stem cells.

Suling Liu | Shivani H Patel | Christophe Ginestier | Ingrid Ibarra | Rachel Martin-Trevino | Shoumin Bai | Sean P McDermott | Li Shang | Jia Ke | Sing J Ou | Amber Heath | Kevin J Zhang | Hasan Korkaya | Shawn G Clouthier | Emmanuelle Charafe-Jauffret | Daniel Birnbaum | Gregory J Hannon | Max S Wicha
PLoS genetics | 2012

MicroRNAs (miRNAs) play important roles in normal cellular differentiation and oncogenesis. microRNA93 (mir-93), a member of the mir106b-25 cluster, located in intron 13 of the MCM7 gene, although frequently overexpressed in human malignancies may also function as a tumor suppressor gene. Using a series of breast cancer cell lines representing different stages of differentiation and mouse xenograft models, we demonstrate that mir-93 modulates the fate of breast cancer stem cells (BCSCs) by regulating their proliferation and differentiation states. In "claudin(low)" SUM159 cells, expression of mir-93 induces Mesenchymal-Epithelial Transition (MET) associated with downregulation of TGFβ signaling and downregulates multiple stem cell regulatory genes, including JAK1, STAT3, AKT3, SOX4, EZH1, and HMGA2, resulting in cancer stem cell (CSC) depletion. Enforced expression of mir-93 completely blocks tumor development in mammary fat pads and development of metastases following intracardiac injection in mouse xenografts. The effect of mir-93 on the CSC population is dependent on the cellular differentiation state, with mir-93 expression increasing the CSC population in MCF7 cells that display a more differentiated "luminal" phenotype. mir-93 also regulates the proliferation and differentiation of normal breast stem cells isolated from reduction mammoplasties. These studies demonstrate that miRNAs can regulate the states and fates of normal and malignant mammary stem cells, findings which have important biological and clinical implications.

Pubmed ID: 22685420

Research resources used in this publication

None found

Antibodies used in this publication

None found

Associated grants

  • Agency: NCI NIH HHS, United States
    Id: CA66233
  • Agency: NCI NIH HHS, United States
    Id: R01 CA101860
  • Agency: NCI NIH HHS, United States
    Id: P30 CA045508
  • Agency: NCI NIH HHS, United States
    Id: CA101860
  • Agency: NCI NIH HHS, United States
    Id: 5 P 30 CA46592

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RRID:SCR_007817

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RRID:SCR_010703

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