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dc.creatorMorcavallo, Alaide
dc.creatorBuraschi, Simone
dc.creatorXu, Shi-Qiong
dc.creatorBelfiore, Antonino
dc.creatorSchaefer, Liliana
dc.creatorIozzo, Renato V.
dc.creatorMorrione, Andrea
dc.date.accessioned2021-11-09T15:40:34Z
dc.date.available2021-11-09T15:40:34Z
dc.date.issued2014-01-02
dc.identifier.citationAlaide Morcavallo, Simone Buraschi, Shi-Qiong Xu, Antonino Belfiore, Liliana Schaefer, Renato V. Iozzo, Andrea Morrione, Decorin differentially modulates the activity of insulin receptor isoform A ligands, Matrix Biology, Volume 35, 2014,Pages 82-90, ISSN 0945-053X, https://doi.org/10.1016/j.matbio.2013.12.010.
dc.identifier.issn0945-053X
dc.identifier.doihttp://dx.doi.org/10.34944/dspace/7070
dc.identifier.urihttp://hdl.handle.net/20.500.12613/7090
dc.description.abstractThe proteoglycan decorin, a key component of the tumor stroma, regulates the action of several tyrosine-kinase receptors, including the EGFR, Met and the IGF-IR. Notably, the action of decorin in regulating the IGF-I system differs between normal and transformed cells. In normal cells, decorin binds with high affinity to both the natural ligand IGF-I and the IGF-I receptor (IGF-IR) and positively regulates IGF-IR activation and downstream signaling. In contrast, in transformed cells, decorin negatively regulates ligand-induced IGF-IR activation, downstream signaling and IGF-IR-dependent biological responses. Whether decorin may bind another member of the IGF-I system, the insulin receptor A isoform (IR-A) and its cognate ligands, insulin, IGF-II and proinsulin, have not been established. Here we show that decorin bound with high affinity insulin and IGF-II and, to a lesser extent, proinsulin and IR-A. We utilized as a cell model system mouse embryonic fibroblasts homozygous for a targeted disruption of the Igf1r gene (designated R− cells) which were stably transfected with a human construct harboring the IR-A isoform of the receptor. Using these R−/IR-A cells, we demonstrate that decorin did not affect ligand-induced phosphorylation of the IR-A but enhanced IR-A downregulation after prolonged IGF-II stimulation without affecting insulin and proinsulin-dependent effects on IR-A stability. In addition, decorin significantly inhibited IGF-II-mediated activation of the Akt pathways, without affecting insulin and proinsulin-dependent signaling. Notably, decorin significantly inhibited IGF-II-mediated cell proliferation of R−/IR-A cells but affected neither insulin- nor proinsulin-dependent mitogenesis. Collectively, these results suggest that decorin differentially regulates the action of IR-A ligands. Decorin preferentially inhibits IGF-II-mediated biological responses but does not affect insulin- or proinsulin-dependent signaling. Thus, decorin loss may contribute to tumor initiation and progression in malignant neoplasms which depend on an IGF-II/IR-A autocrine loop.
dc.format.extent9 pages
dc.languageEnglish
dc.language.isoeng
dc.relation.ispartofFaculty/ Researcher Works
dc.relation.haspartMatrix Biology, Vol. 35
dc.relation.isreferencedbyElsevier
dc.rightsAttribution-NonCommercial-NoDerivs CC BY-NC-ND
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectDecorin
dc.subjectIR-A
dc.subjectSignaling
dc.subjectProliferation
dc.titleDecorin differentially modulates the activity of insulin receptor isoform A ligands
dc.typeText
dc.type.genreJournal article
dc.description.departmentBiology
dc.relation.doihttps://doi.org/10.1016/j.matbio.2013.12.010
dc.ada.noteFor Americans with Disabilities Act (ADA) accommodation, including help with reading this content, please contact scholarshare@temple.edu
dc.description.schoolcollegeTemple University. College of Science and Technology
dc.creator.orcidMorrione|0000-0002-2319-7884
dc.temple.creatorMorrione, Andrea
refterms.dateFOA2021-11-09T15:40:34Z


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