Publication
Role of VEGFA, CXCR4 and VHL mutation in tumour behaviour
Kruizinga, R., 2014, [S.l.]: s.n.. 147 p.Research output: Thesis › Thesis fully internal (DIV)

Documents
- Title and contents
Final publisher's version, 227 KB, PDF document
- Chapter 1
Final publisher's version, 579 KB, PDF document
- Chapter 2
Final publisher's version, 544 KB, PDF document
- Chapter 3
Final publisher's version, 607 KB, PDF document
- Chapter 4
Final publisher's version, 316 KB, PDF document
- Chapter 5
Final publisher's version, 1.26 MB, PDF document
- Chapter 6
Final publisher's version, 431 KB, PDF document
- Chapter 7
Final publisher's version, 296 KB, PDF document
- Summary, Discussion and Future perspectives
Final publisher's version, 217 KB, PDF document
- Nederlandse samenvatting, dankwoord, Lijst van publicaties
Final publisher's version, 240 KB, PDF document
- Complete dissertation
Final publisher's version, 3.03 MB, PDF document
Von Hippel Lindau (VHL) disease is rare cancer syndrome. VHL disease patients develop both benign and malignant vascularised tumours. A loss-of-function of the VHL protein in VHL-disease causes increased transcription of vascular endothelial growth factor (VEGF-A), and chemokine receptor 4 (CXCR4). The aim of this thesis was to elucidate clinical features and shed more light on the behaviour of VHL-disease. In addition, the role of CXCR4 in VHL-disease and VEGFA in AML, acute myeloid leukaemia, was studied. The most important results of our research were the ability to calculate when patients will develop their first tumour by using statistical models and that intensified surveillance in pregnancy was needed. We performed a literature search that indicated the important role of CXCR4 in the interaction with the cancer micro-environment in addition to the role in metastasis. By interaction with the microenvironment cancer cells might become insensitive to standard chemotherapy. In paediatric AML we found that the measured levels of the mRNA VEGFA isoforms had no prognostic value. In addition, we found that CXCR4 and VEGFA have a higher expression in haemangioblastoma tissue compared to normal brain tissue. Moreover, CXCR4 was not expressed in normal brain tissue. These results encourage future research on treatment opportunities with drugs specifically targeting CXCR4 and VEGFA in VHL-related tumours.
Translated title of the contribution | Rol van VEGFA, CXCR4 en VHL mutatie in tumor karakter |
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Original language | English |
Qualification | Doctor of Philosophy |
Awarding Institution | |
Supervisors/Advisors |
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Award date | 28-Apr-2014 |
Place of Publication | [S.l.] |
Publisher | |
Print ISBNs | 978-90-367-6876-4 |
Electronic ISBNs | 978-90-367-6875-7 |
Publication status | Published - 2014 |
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