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dc.contributor.authorZhu, W
dc.contributor.authorGliddon, BL
dc.contributor.authorJarman, KE
dc.contributor.authorMoretti, PAB
dc.contributor.authorTin, T
dc.contributor.authorParise, LV
dc.contributor.authorWoodcock, JM
dc.contributor.authorPowell, JA
dc.contributor.authorRuszkiewicz, A
dc.contributor.authorPitman, MR
dc.contributor.authorPitson, SM
dc.date.accessioned2021-04-26T01:43:52Z
dc.date.available2021-04-26T01:43:52Z
dc.date.issued2017-05-04
dc.identifierpii: onc2016428
dc.identifier.citationZhu, W., Gliddon, B. L., Jarman, K. E., Moretti, P. A. B., Tin, T., Parise, L. V., Woodcock, J. M., Powell, J. A., Ruszkiewicz, A., Pitman, M. R. & Pitson, S. M. (2017). CIB1 contributes to oncogenic signalling by Ras via modulating the subcellular localisation of sphingosine kinase 1.. Oncogene, 36 (18), pp.2619-2627. https://doi.org/10.1038/onc.2016.428.
dc.identifier.issn0950-9232
dc.identifier.urihttp://hdl.handle.net/11343/269753
dc.description.abstractCIB1 (calcium and integrin binding protein 1) is a small intracellular protein with numerous interacting partners, and hence has been implicated in various cellular functions. Recent studies have revealed emerging roles of CIB1 in regulating cancer cell survival and angiogenesis, although the mechanisms involved have remained largely undefined. In investigating the oncogenic function of CIB1, we initially found that CIB1 is widely up-regulated across a diverse range of cancers, with this upregulation frequently correlating with oncogenic mutations of KRas. Consistent with this, we found that ectopic expression of oncogenic KRas and HRas in cells resulted in elevated CIB1 expression. We previously described the Ca2+-myristoyl switch function of CIB1, and its ability to facilitate agonist-induced plasma membrane localisation of sphingosine kinase 1 (SK1), a location where SK1 is known to elicit oncogenic signalling. Thus, we examined the role this may play in oncogenesis. Consistent with these findings, we demonstrated here that over-expression of CIB1 by itself is sufficient to drive localisation of SK1 to the plasma membrane and enhance the membrane-associated enzymatic activity of SK1, as well as its oncogenic signalling. We subsequently demonstrated that elevated levels of CIB1 resulted in full neoplastic transformation, in a manner dependent on SK1. In agreement with our previous findings that SK1 is a downstream mediator of oncogenic signalling by Ras, we found that targeting CIB1 also inhibited neoplastic growth of cells induced by oncogenic Ras, suggesting an important pro-tumorigenic role for CIB1. Thus, we have demonstrated for the first time a role for CIB1 in neoplastic transformation, and revealed a novel mechanism facilitating oncogenic signalling by Ras and SK1.
dc.languageeng
dc.publisherSpringer Science and Business Media LLC
dc.titleCIB1 contributes to oncogenic signalling by Ras via modulating the subcellular localisation of sphingosine kinase 1.
dc.typeJournal Article
dc.identifier.doi10.1038/onc.2016.428
melbourne.affiliation.departmentMedical Biology (W.E.H.I.)
melbourne.affiliation.departmentCentre for Cancer Research
melbourne.affiliation.facultyMedicine, Dentistry & Health Sciences
melbourne.source.titleOncogene
melbourne.source.volume36
melbourne.source.issue18
melbourne.source.pages2619-2627
melbourne.elementsid1320519
melbourne.openaccess.urlhttps://europepmc.org/articles/PMC5418080?pdf=render
melbourne.openaccess.pmchttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC5418080
melbourne.openaccess.statusPublished version
melbourne.contributor.authorJarman, Kate
melbourne.contributor.authorZhu, Wenying
dc.identifier.eissn1476-5594
melbourne.accessrightsAccess this item via the Open Access location


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