Linking CREB function with altered metabolism in murine fibroblast-based model cell lines.
Ontology highlight
ABSTRACT: The cAMP-responsive element binding protein CREB is frequently overexpressed and activated in tumors of distinct histology, leading to enhanced proliferation, migration, invasion and angiogenesis as well as reduced apoptosis. The de-regulated expression of CREB might be linked with transcriptional as well as post-transcriptional regulation mechanisms. We show here that altered CREB expression levels and function are associated with changes in the cellular metabolism. Using comparative proteome-based analysis an altered expression pattern of proteins involved in the cellular metabolism in particular in glycolysis was found upon CREB down-regulation in HER-2/neu-transfected cell lines. This was associated with diminished expression levels of the glucose transporter 1, reduced glucose uptake
SUBMITTER: Steven A
PROVIDER: S-EPMC5722575 | biostudies-literature | 2017 Nov
REPOSITORIES: biostudies-literature
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