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Slug and Sox9 Cooperatively Determine the Mammary Stem Cell State
Author(s) -
Wenjun Guo,
Zuzana Keckesova,
Joana Liu Donaher,
Tsukasa Shibue,
Verena Tischler,
Ferenc Reinhardt,
Shalev Itzkovitz,
Aurelia Noske,
Ursina ZürrerHärdi,
George W. Bell,
Wai Leong Tam,
Sendurai A. Mani,
Alexander van Oudenaarden,
Robert A. Weinberg
Publication year - 2012
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.2012.02.008
Subject(s) - biology , slug , sox9 , stem cell , microbiology and biotechnology , state (computer science) , computational biology , genetics , evolutionary biology , transcription factor , gene , ecology , algorithm , computer science
Regulatory networks orchestrated by key transcription factors (TFs) have been proposed to play a central role in the determination of stem cell states. However, the master transcriptional regulators of adult stem cells are poorly understood. We have identified two TFs, Slug and Sox9, that act cooperatively to determine the mammary stem cell (MaSC) state. Inhibition of either Slug or Sox9 blocks MaSC activity in primary mammary epithelial cells. Conversely, transient coexpression of exogenous Slug and Sox9 suffices to convert differentiated luminal cells into MaSCs with long-term mammary gland-reconstituting ability. Slug and Sox9 induce MaSCs by activating distinct autoregulatory gene expression programs. We also show that coexpression of Slug and Sox9 promotes the tumorigenic and metastasis-seeding abilities of human breast cancer cells and is associated with poor patient survival, providing direct evidence that human breast cancer stem cells are controlled by key regulators similar to those operating in normal murine MaSCs.

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