Abstract
Twist is a key transcription factor for Epithelial-mesenchymal transition (EMT), which is a cellular de-differentiation program that promotes invasion and metastasis, confers tumor cells with cancer stem cell (CSC)-like characteristics, and increases therapeutic resistance. However, the mechanisms that facilitate the functions of Twist remain unclear. Here we report that Twist overexpression increased expression of PAR1, an upstream regulator of the Hippo pathway; PAR1 promotes invasion, migration, and CSC-like properties in breast cancer by activating the transcriptional co-activator TAZ. Our study indicates that Hippo pathway inhibition is required for the increased migratory and invasiveness ability of breast cancer cells in Twist-mediated EMT.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, Non-P.H.S.
MeSH terms
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Apoptosis / genetics
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Breast Neoplasms / genetics
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Breast Neoplasms / metabolism*
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Breast Neoplasms / pathology*
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Cell Line, Tumor
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Cell Movement / genetics
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Cell Survival / genetics
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Epithelial-Mesenchymal Transition* / genetics
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Female
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Gene Expression
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Gene Knockdown Techniques
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Hippo Signaling Pathway
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Humans
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Neoplasm Invasiveness
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Protein Serine-Threonine Kinases / metabolism*
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Signal Transduction*
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Snail Family Transcription Factors / genetics
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Snail Family Transcription Factors / metabolism
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Twist Transcription Factors / genetics
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Twist Transcription Factors / metabolism
Substances
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Snail Family Transcription Factors
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Twist Transcription Factors
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Protein Serine-Threonine Kinases