Cross-talk and modulation of signaling between somatostatin and growth factor receptors
- PMID: 21870170
- DOI: 10.1007/s12020-011-9524-8
Cross-talk and modulation of signaling between somatostatin and growth factor receptors
Abstract
The process of homo- and/or heterodimerization of G-protein coupled receptors (GPCRs) and receptor tyrosine kinase (RTK) families are crucial for implicating the fundamental properties of receptor proteins including receptor expression, trafficking, and desensitization as well as signal transduction. The members of GPCR and RTK family constitute largest cell surface receptor proteins and regulate physiological functions of cells in response to external and internal stimuli. Notably, GPCRs and RTKs play major role in regulation of several key cellular functions which are associated with several pathological conditions including cancer biology, neurodegenerative and cardiovascular diseases. The focus of this review is to highlight the recent findings on the possible cross-talk between somatostatin receptors (members of GPCR family) and growth factor receptors like epidermal growth factor receptors (members of RTK family). Furthermore, functional consequences of such an interaction in modulation of signaling pathways linked to pathological conditions specifically in cancer are discussed.
Similar articles
-
Signal transduction pathways of G protein-coupled receptors and their cross-talk with receptor tyrosine kinases: lessons from bradykinin signaling.Curr Med Chem. 2000 Sep;7(9):911-43. doi: 10.2174/0929867003374589. Curr Med Chem. 2000. PMID: 10911023 Review.
-
Somatostatin receptors 1 and 5 heterodimerize with epidermal growth factor receptor: agonist-dependent modulation of the downstream MAPK signalling pathway in breast cancer cells.Cell Signal. 2009 Mar;21(3):428-39. doi: 10.1016/j.cellsig.2008.11.012. Epub 2008 Dec 3. Cell Signal. 2009. PMID: 19070659
-
Somatostatin receptor 5 is a prominent regulator of signaling pathways in cells with coexpression of Cannabinoid receptors 1.Neuroscience. 2017 Jan 6;340:218-231. doi: 10.1016/j.neuroscience.2016.10.056. Epub 2016 Oct 29. Neuroscience. 2017. PMID: 27984180
-
Microbead arrays for the analysis of ErbB receptor tyrosine kinase activation and dimerization in breast cancer cells.Assay Drug Dev Technol. 2010 Feb;8(1):27-36. doi: 10.1089/adt.2009.0208. Assay Drug Dev Technol. 2010. PMID: 20035613 Free PMC article.
-
Cell-surface receptors transactivation mediated by g protein-coupled receptors.Int J Mol Sci. 2014 Oct 29;15(11):19700-28. doi: 10.3390/ijms151119700. Int J Mol Sci. 2014. PMID: 25356505 Free PMC article. Review.
Cited by
-
Crosstalk between the renin-angiotensin system and the advance glycation end product axis in the heart: role of the cardiac fibroblast.J Cardiovasc Transl Res. 2012 Dec;5(6):805-13. doi: 10.1007/s12265-012-9405-4. Epub 2012 Sep 29. J Cardiovasc Transl Res. 2012. PMID: 23054657 Review.
-
International Union of Basic and Clinical Pharmacology. CV. Somatostatin Receptors: Structure, Function, Ligands, and New Nomenclature.Pharmacol Rev. 2018 Oct;70(4):763-835. doi: 10.1124/pr.117.015388. Pharmacol Rev. 2018. PMID: 30232095 Free PMC article. Review.
-
Pathophysiology of GPCR Homo- and Heterodimerization: Special Emphasis on Somatostatin Receptors.Pharmaceuticals (Basel). 2012 Apr 27;5(5):417-46. doi: 10.3390/ph5050417. Pharmaceuticals (Basel). 2012. PMID: 24281555 Free PMC article.
-
Exploiting cancer's phenotypic guise against itself: targeting ectopically expressed peptide G-protein coupled receptors for lung cancer therapy.Oncotarget. 2017 Jun 7;8(61):104615-104637. doi: 10.18632/oncotarget.18403. eCollection 2017 Nov 28. Oncotarget. 2017. PMID: 29262666 Free PMC article. Review.
-
Interrogating tumor metabolism and tumor microenvironments using molecular positron emission tomography imaging. Theranostic approaches to improve therapeutics.Pharmacol Rev. 2013 Sep 24;65(4):1214-56. doi: 10.1124/pr.113.007625. Print 2013. Pharmacol Rev. 2013. PMID: 24064460 Free PMC article. Review.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources