Abstract
Glioma-initiating cells (GICs) are responsible for the initiation and recurrence of gliomas. Here, we identify a molecular mechanism that regulates the self-renewal capacity of patient-derived GICs. We show that TGF-beta and LIF induce the self-renewal capacity and prevent the differentiation of GICs. TGF-beta induces the self-renewal capacity of GICs, but not of normal human neuroprogenitors, through the Smad-dependent induction of LIF and the subsequent activation of the JAK-STAT pathway. The effect of TGF-beta and LIF on GICs promotes oncogenesis in vivo. Some human gliomas express high levels of LIF that correlate with high expression of TGF-beta2 and neuroprogenitor cell markers. Our results show that TGF-beta and LIF have an essential role in the regulation of GICs in human glioblastoma.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Brain Neoplasms / genetics
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Brain Neoplasms / metabolism
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Brain Neoplasms / pathology
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Cell Differentiation*
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Cells, Cultured
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Glioblastoma / genetics
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Glioblastoma / metabolism*
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Glioblastoma / pathology
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Humans
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Janus Kinase 1 / genetics
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Janus Kinase 1 / metabolism
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Leukemia Inhibitory Factor / genetics
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Leukemia Inhibitory Factor / metabolism*
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Mice
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Mice, Inbred NOD
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Mice, SCID
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Neurons / cytology*
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Neurons / metabolism
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Promoter Regions, Genetic
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STAT Transcription Factors / genetics
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STAT Transcription Factors / metabolism
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Signal Transduction
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Smad3 Protein / genetics
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Smad3 Protein / metabolism
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Stem Cells / metabolism
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Transforming Growth Factor beta / genetics
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Transforming Growth Factor beta / metabolism*
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Transforming Growth Factor beta2 / genetics
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Transforming Growth Factor beta2 / metabolism
Substances
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LIF protein, human
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Leukemia Inhibitory Factor
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STAT Transcription Factors
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Smad3 Protein
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Transforming Growth Factor beta
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Transforming Growth Factor beta2
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JAK1 protein, human
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Janus Kinase 1