Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/106818
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Type: Journal article
Title: CIB1 contributes to oncogenic signalling by Ras via modulating the subcellular localisation of sphingosine kinase 1
Author: Zhu, W.
Gliddon, B.
Jarman, K.
Moretti, P.
Tin, T.
Parise, L.
Woodcock, J.
Powell, J.
Ruszkiewicz, A.
Pitman, M.
Pitson, S.
Citation: Oncogene, 2017; 36(18):2619-2627
Publisher: Nature Publishing Group
Issue Date: 2017
ISSN: 0950-9232
1476-5594
Statement of
Responsibility: 
W Zhu, BL Gliddon, KE Jarman, PAB Moretti, T Tin, LV Parise, JM Woodcock, JA Powell, A Ruszkiewicz, MR Pitman, and SM Pitson
Abstract: CIB1 (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.
Keywords: Cell Line, Tumor; Cell Membrane; Humans; Neoplasms; Calcium; Phosphotransferases (Alcohol Group Acceptor); Calcium-Binding Proteins; Cell Survival; Gene Expression Regulation, Neoplastic; Proto-Oncogene Proteins p21(ras); Carcinogenesis
Rights: © 2017 Macmillan Publishers Limited, part of Springer Nature. All rights reserved
RMID: 0030059893
DOI: 10.1038/onc.2016.428
Grant ID: http://purl.org/au-research/grants/nhmrc/508098
http://purl.org/au-research/grants/nhmrc/1042589
Appears in Collections:Medicine publications

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