Journal article

Selective CREB-dependent cyclin expression mediated by the PI3K and MAPK pathways supports glioma cell proliferation

P Daniel, G Filiz, DV Brown, F Hollande, M Gonzales, G D'Abaco, N Papalexis, WA Phillips, J Malaterre, RG Ramsay, T Mantamadiotis

Oncogenesis | Published : 2014

Abstract

The cyclic-AMP response element binding (CREB) protein has been shown to have a pivotal role in cell survival and cell proliferation. Transgenic rodent models have revealed a role for CREB in higher-order brain functions, such as memory and drug addiction behaviors. CREB overexpression in transgenic animals imparts oncogenic properties on cells in various tissues, and aberrant CREB expression is associated with tumours. It is the central position of CREB, downstream from key developmental and growth signalling pathways, which gives CREB this ability to influence a spectrum of cellular activities, such as cell survival, growth and differentiation, in both normal and cancer cells. We show that..

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Grants

Awarded by National Health and Medical Research Council


Funding Acknowledgements

We thank the members of the Department of Pathology, TheUniversityofMelbourne, Parkville, Victoria, Australia for the use of equipment and reagents, especially Dr Genevieve Evin, Dr Vicki Lawson, Laura Ellett and Janine James. We also thank Professor Paul Waring for financial support for PD, GF and DVB and the Cell Signaling Laboratory. Part of this work was also supported by an EU-FP7-PEOPLE Marie Curie IRG (Neurogencreb 231032) grant to TM. WAP, RGR and JM were supported, in part, by project grants from the National Health and Medical Research Council of Australia.