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• W2130854580 startingPage "203" @default.
• W2130854580 abstract "Recent discoveries suggest that several protein kinases are rapidly activated in response to ligand binding to cytoplasmic steroid hormone receptors (SRs), including progesterone receptors (PRs). Thus, PRs act as ligand-activated transcription factor sensors for growth factor-initiated signaling pathways in hormonally regulated tissues, such as the breast. Induction of rapid signaling upon progestin binding to PR-B provides a means to ensure that receptors and co-regulators are appropriately phosphorylated as part of optimal transcription complexes. Alternatively, PR-B activated kinase cascades provide additional avenues for progestin-regulated gene expression independent of PR nuclear action. Herein, an overview of progesterone/PR and signaling cross-talk in breast cancer models is provided. Kinases are emerging as key mediators of PR action. Cross-talk between SR and membrane-initiated signaling events suggests a mechanism for coordinate regulation of gene subsets by mitogenic stimuli in hormonally responsive normal tissues, and is suspected to contribute to cancer biology." @default.
• W2130854580 created "2016-06-24" @default.
• W2130854580 creator A5051915371 @default.
• W2130854580 date "2008-02-01" @default.
• W2130854580 modified "2023-09-25" @default.
• W2130854580 title "Integration of progesterone receptor action with rapid signaling events in breast cancer models" @default.
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• W2130854580 doi "https://doi.org/10.1016/j.jsbmb.2007.09.019" @default.
• W2130854580 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2330263" @default.
• W2130854580 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/17964138" @default.
• W2130854580 hasPublicationYear "2008" @default.
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