Phosphorylation of a splice variant of collapsin response mediator protein 2 in the nucleus of tumour cells links cyclin dependent kinase-5 to oncogenesis

BMC Cancer

Research Article

Nicholas A. Morrice¹  Francis A. Carey²  Yvonne L. Woods²  Susan E. Bray³  Philip J. Coates³  Calum Sutherland⁴  Nicola J. Grant⁴  C. James Hastie⁵  Douglas J. Lamont⁶ 

[1] Beatson Cancer Institute, Glasgow, UK;Department of Pathology, Ninewells Hospital, NHS Tayside, Dundee, UK;Division of Cancer, University of Dundee, Dundee, UK;Division of Cardiovascular and Diabetes Medicine, University of Dundee, Ninewells Medical School, DD1 9SY, Dundee, UK;Division of Signal Transduction and Therapy, University of Dundee, Dundee, UK;FingerPrints Proteomics Facility, University of Dundee, Dundee, UK;

关键词: Phosphorylation;    Lung cancer;    Breast cancer;    Lymphoma;    Biomarker;   

DOI  :  10.1186/s12885-015-1691-1

 received in 2015-05-25, accepted in 2015-10-07,  发布年份 2015

来源: Springer

【 摘 要 】

BackgroundCyclin-dependent protein kinase-5 (CDK5) is an unusual member of the CDK family as it is not cell cycle regulated. However many of its substrates have roles in cell growth and oncogenesis, raising the possibility that CDK5 modulation could have therapeutic benefit. In order to establish whether changes in CDK5 activity are associated with oncogenesis one could quantify phosphorylation of CDK5 targets in disease tissue in comparison to appropriate controls. However the identity of physiological and pathophysiological CDK5 substrates remains the subject of debate, making the choice of CDK5 activity biomarkers difficult.MethodsHere we use in vitro and in cell phosphorylation assays to identify novel features of CDK5 target sequence determinants that confer enhanced CDK5 selectivity, providing means to select substrate biomarkers of CDK5 activity with more confidence. We then characterize tools for the best CDK5 substrate we identified to monitor its phosphorylation in human tissue and use these to interrogate human tumour arrays.ResultsThe close proximity of Arg/Lys amino acids and a proline two residues N-terminal to the phosphorylated residue both improve recognition of the substrate by CDK5. In contrast the presence of a proline two residues C-terminal to the target residue dramatically reduces phosphorylation rate. Serine-522 of Collapsin Response Mediator-2 (CRMP2) is a validated CDK5 substrate with many of these structural criteria. We generate and characterise phosphospecific antibodies to Ser522 and show that phosphorylation appears in human tumours (lung, breast, and lymphoma) in stark contrast to surrounding non-neoplastic tissue. In lung cancer the anti-phospho-Ser522 signal is positive in squamous cell carcinoma more frequently than adenocarcinoma. Finally we demonstrate that it is a specific and unusual splice variant of CRMP2 (CRMP2A) that is phosphorylated in tumour cells.ConclusionsFor the first time this data associates altered CDK5 substrate phosphorylation with oncogenesis in some but not all tumour types, implicating altered CDK5 activity in aspects of pathogenesis. These data identify a novel oncogenic mechanism where CDK5 activation induces CRMP2A phosphorylation in the nuclei of tumour cells.

【 授权许可】

CC BY   
© Grant et al. 2015