Unknown

Dataset Information

0

Normal and cancerous mammary stem cells evade interferon-induced constraint through the miR-199a-LCOR axis.


ABSTRACT: Tumour-initiating cells, or cancer stem cells (CSCs), possess stem-cell-like properties observed in normal adult tissue stem cells. Normal and cancerous stem cells may therefore share regulatory mechanisms for maintaining self-renewing capacity and resisting differentiation elicited by cell-intrinsic or microenvironmental cues. Here, we show that miR-199a promotes stem cell properties in mammary stem cells and breast CSCs by directly repressing nuclear receptor corepressor LCOR, which primes interferon (IFN) responses. Elevated miR-199a expression in stem-cell-enriched populations protects normal and malignant stem-like cells from differentiation and senescence induced by IFNs that are produced by epithelial and immune cells in the mammary gland. Importantly, the miR-199a-LCOR-IFN axis is activated in poorly differentiated ER- breast tumours, functionally promotes tumour initiation and metastasis, and is associated with poor clinical outcome. Our study therefore reveals a common mechanism shared by normal and malignant stem cells to protect them from suppressive immune cytokine signalling.

SUBMITTER: Celia-Terrassa T 

PROVIDER: S-EPMC5481166 | biostudies-literature | 2017 Jun

REPOSITORIES: biostudies-literature

altmetric image

Publications


Tumour-initiating cells, or cancer stem cells (CSCs), possess stem-cell-like properties observed in normal adult tissue stem cells. Normal and cancerous stem cells may therefore share regulatory mechanisms for maintaining self-renewing capacity and resisting differentiation elicited by cell-intrinsic or microenvironmental cues. Here, we show that miR-199a promotes stem cell properties in mammary stem cells and breast CSCs by directly repressing nuclear receptor corepressor LCOR, which primes int  ...[more]

Similar Datasets

2017-05-05 | GSE85808 | GEO
| PRJNA339441 | ENA
| S-EPMC6819876 | biostudies-literature
2017-05-05 | GSE85629 | GEO
| S-EPMC55532 | biostudies-literature
| S-EPMC9695915 | biostudies-literature
| S-EPMC8018440 | biostudies-literature
| S-EPMC8824889 | biostudies-literature
| S-EPMC7228945 | biostudies-literature
| S-EPMC5619986 | biostudies-literature