Role of microRNA221 in regulating normal mammary epithelial hierarchy and breast cancer stem-like cells

Jia Ke, Zhiju Zhao, Su Hyung Hong, Shoumin Bai, Zhen He, Fayaz Malik, Jiahui Xu, Lei Zhou, Weilong Chen, Rachel Martin-Trevino, Xiaojian Wu, Ping Lan, Yongju Yi, Christophe Ginestier, Ingrid Ibarra, Li Shang, Sean McDermott, Tahra Luther, Shawn G. Clouthier, Max S. WichaSuling Liu

Research output: Contribution to journalArticlepeer-review

52 Scopus citations

Abstract

Increasing evidence suggests that lineage specific subpopulations and stem-like cells exist in normal and malignant breast tissues. Epigenetic mechanisms maintaining this hierarchical homeostasis remain to be investigated. In this study, we found the level of microRNA221 (miR-221) was higher in stem-like and myoepithelial cells than in luminal cells isolated from normal and malignant breast tissue. In normal breast cells, over-expression of miR-221 generated more myoepithelial cells whereas knockdown of miR-221 increased luminal cells. Over-expression of miR-221 stimulated stem-like cells in luminal type of cancer and the miR-221 level was correlated with clinical outcome in breast cancer patients. Epithelial-mesenchymal transition (EMT) was induced by overexpression of miR-221 in normal and breast cancer cells. The EMT related gene ATXN1 was found to be a miR-221 target gene regulating breast cell hierarchy. In conclusion, we propose that miR-221 contributes to lineage homeostasis of normal and malignant breast epithelium.

Original languageEnglish
Pages (from-to)3709-3721
Number of pages13
JournalOncotarget
Volume6
Issue number6
DOIs
StatePublished - 2015

Keywords

  • Breast stem-like cells
  • Differentiation
  • Hierarchy
  • miR-221

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