Abstract
Pancreatic adenocarcinoma is one of the most aggressive human cancers. It displays many different chromosomal abnormalities and mutations. To design new therapeutic strategies, it is important to identify the signaling pathways and gene networks within this apparent complexity that are predominantly altered. The TGFβ signaling pathway and associated transcription network emerges as a central actor of pancreatic oncogenesis. Its tumor suppressor function in this tissue can be affected by several alterations.
Publication types
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Research Support, Non-U.S. Gov't
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Review
MeSH terms
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DNA-Binding Proteins
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GATA6 Transcription Factor / genetics
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GATA6 Transcription Factor / metabolism
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Humans
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Models, Biological
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Nuclear Proteins / genetics
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Nuclear Proteins / metabolism
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Pancreatic Neoplasms / genetics
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Pancreatic Neoplasms / metabolism*
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Signal Transduction / genetics
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Signal Transduction / physiology
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Transcription Factors / genetics
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Transcription Factors / metabolism
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Transforming Growth Factor beta / genetics
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Transforming Growth Factor beta / metabolism*
Substances
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ARID1A protein, human
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DNA-Binding Proteins
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GATA6 Transcription Factor
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GATA6 protein, human
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Nuclear Proteins
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Transcription Factors
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Transforming Growth Factor beta