An investigation into the role of Rab-Coupling Protein and EphA2 during cancer cell migration

Gundry, Christine (2015) An investigation into the role of Rab-Coupling Protein and EphA2 during cancer cell migration. PhD thesis, University of Glasgow.

Due to Embargo and/or Third Party Copyright restrictions, this thesis is not available in this service.

Abstract

The gene encoding Rab-Coupling Protein (RCP), a Rab11 GTPase effector, is found on a chromosomal locus that is frequently amplified in cancer. We have previously shown that RCP drives alpha5beta1-integrin and EGFR recycling to the plasma membrane, thus contributing to the invasive migration of tumour cells. Using MALDI-TOF mass spectrometry, I have identified EphA2 and two Rab GTPases, Rab6 and Rab14, as novel RCP-associated proteins. Immunoprecipitation-based studies confirm these associations using several different cancer cell lines. EphA2 is a receptor tyrosine kinase (RTK) that is required for contact inhibition of locomotion (CIL), and this process is thought to contribute to cancer cell invasion. To determine whether the EphA2-RCP association has functional significance, I tested whether RCP, Rab GTPases and other Rab11 effector proteins are required for CIL. siRNA knockdown of either RCP or Rab14 prevented efficient CIL, but depletion of Rab11 or Fip2 expression was ineffective in this regard. Likewise, HGF-induced scattering of cell colonies was opposed by suppression of EphA2, RCP or Rab14 expression. Since RCP and Rab14 are involved in RTK trafficking, EphA2 internalisation kinetics were investigated. HGF increased EphA2 trafficking in an RCP- and Rab14-dependent fashion. Live cell imaging demonstrated that EphA2 is delivered to an RCP and Rab14 positive compartment upon HGF treatment. Furthermore, HGF drove phosphorylation of RCP on Serine435, which enhanced the association between EphA2, RCP and Rab14. Indeed, mutating the phosphor-acceptor site on RCP (RCPS435A) reduced its association with EphA2 and Rab14, and blocked HGF-driven cell scattering. EphA2 is frequently overexpressed in human pancreatic cancer and this is associated with poor patient prognosis. The role of EphA2 and RCP in metastasis was investigated in an autochthonous model of pancreatic ductal adenocarcinoma (PDAC) by crossing EphA2-/- and RCPfl/fl mice into the KPC (Pdx1-Cre, KrasG12D/+, p53R172H/+) PDAC model. Indeed, ablation of EphA2 or RCP expression in the mouse pancreas reduced the formation of liver metastases. Furthermore, PDAC lines from KPC EphA2-/- and KPC RCPfl/fl mice had a less scattered phenotype and were less invasive in vitro thus corroborating the observations indicating that EphA2 and RCP have an important role in cell-cell repulsion.

Item Type: Thesis (PhD)
Qualification Level: Doctoral
Keywords: EphA2, RCP, Rab14, contact inhibition of locomotion, cell-cell repulsion
Subjects: Q Science > QH Natural history > QH301 Biology
Colleges/Schools: College of Medical Veterinary and Life Sciences > Institute of Cancer Sciences > Beatson Institute of Cancer Research
Funder's Name: UNSPECIFIED
Supervisor's Name: Norman, Professor Jim
Date of Award: 2015
Embargo Date: 24 March 2018
Depositing User: Mrs Christine Gundry
Unique ID: glathesis:2015-6217
Copyright: Copyright of this thesis is held by the author.
Date Deposited: 01 Apr 2015 09:00
Last Modified: 07 Apr 2015 15:20
URI: http://theses.gla.ac.uk/id/eprint/6217

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