Mapping of EGFR treatment effects and uncovering DNA repair mechanisms using quantitative proteomics

de Boer, H. R., 2017, [Groningen]: Rijksuniversiteit Groningen. 180 p.

Research output: ThesisThesis fully internal (DIV)Academic

Copy link to clipboard


  • Title and contents

    Final publisher's version, 164 KB, PDF-document

  • Chapter 1

    Final publisher's version, 252 KB, PDF-document

  • Chapter 2

    Final publisher's version, 4 MB, PDF-document

  • Chapter 3

    Final publisher's version, 22 MB, PDF-document

  • Chapter 4

    Final publisher's version, 3 MB, PDF-document

  • Chapter 5

    Final publisher's version, 1 MB, PDF-document

  • Chapter 6

    Final publisher's version, 5 MB, PDF-document

  • Chapter 7

    Final publisher's version, 5 MB, PDF-document

  • Chapter 8

    Final publisher's version, 740 KB, PDF-document

  • Complete thesis

    Final publisher's version, 38 MB, PDF-document

  • Propositions

    Final publisher's version, 267 KB, PDF-document

In this thesis, we aimed to determine at the proteomic level how cancer cells deal with therapeutic targeting of cancer-inducing pathways or supporting non-cancerous pathways. To this end, we combined quantitative proteomics, the study of all proteins in cells, with a range of cell biological and genetic techniques to uncover mechanisms and markers of treatment efficacy. In these proteomics studies we made a number of discoveries.
First off, we found that cells start to produce the protein Mucin-1 (MUC1) after they are treated with an inhibitor of EGFR, a growth factor receptor. We could also measure this increase in MUC1 in the blood plasma of tumor-bearing mice after they were treated with the EGFR inhibitor. We hope that in the future this can be used in cancer patients to determine if treatment with EGFR inhibitors is successful.
In a second proteomics analysis we searched for proteins that would be degraded by the protein complex APC/C-Cdh1 after cells have finished dividing. Here we found that the protein CtIP, which is part of DNA repair processes, was degraded by the APC/C-Cdh1 after cell division, but also when DNA was damaged by irradiation.
As a final result we found a new role of the protein Rif1. We found that this protein was required during cell divisions to process intertwined or non-replicated DNA. This processing is required to make sure that cell division are finished without damage to the DNA.
Original languageEnglish
QualificationDoctor of Philosophy
Awarding Institution
Award date13-Dec-2017
Place of Publication[Groningen]
Print ISBNs978-94-034-0298-7
Electronic ISBNs978-94-034-0297-0
Publication statusPublished - 2017

View graph of relations

Download statistics

No data available

ID: 51420906