Downregulation of miRNA-200c Links Breast Cancer Stem Cells with Normal Stem Cells
Author(s) -
Yohei Shimono,
Maider Zabala,
Robert W. Cho,
Neethan A. Lobo,
Piero Dalerba,
Dalong Qian,
Maximilian Diehn,
Huiping Liu,
Sarita Panula,
Eric Chiao,
Frederick M. Dirbas,
George Somlo,
Renee A. Reijo Pera,
Kaiqin Lao,
Michael F. Clarke
Publication year - 2009
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2009.07.011
Subject(s) - biology , downregulation and upregulation , stem cell , microrna , cancer stem cell , cancer research , microbiology and biotechnology , genetics , gene
Human breast tumors contain a breast cancer stem cell (BCSC) population with properties reminiscent of normal stem cells. We found 37 microRNAs that were differentially expressed between human BCSCs and nontumorigenic cancer cells. Three clusters, miR-200c-141, miR-200b-200a-429, and miR-183-96-182 were downregulated in human BCSCs, normal human and murine mammary stem/progenitor cells, and embryonal carcinoma cells. Expression of BMI1, a known regulator of stem cell self-renewal, was modulated by miR-200c. miR-200c inhibited the clonal expansion of breast cancer cells and suppressed the growth of embryonal carcinoma cells in vitro. Most importantly, miR-200c strongly suppressed the ability of normal mammary stem cells to form mammary ducts and tumor formation driven by human BCSCs in vivo. The coordinated downregulation of three microRNA clusters and the similar functional regulation of clonal expansion by miR-200c provide a molecular link that connects BCSCs with normal stem cells.
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