User profiles for Olaf van Tellingen

Olaf van Tellingen

Netherlands Cancer Institute
Verified email at nki.nl
Cited by 24503

[HTML][HTML] Knockout of cytochrome P450 3A yields new mouse models for understanding xenobiotic metabolism

…, MA van der Valk, O van Tellingen… - The Journal of …, 2007 - Am Soc Clin Investig
Cytochrome P450 3A (CYP3A) enzymes constitute an important detoxification system that
contributes to primary metabolism of more than half of all prescribed medications. To …

Modulation of the blood–brain barrier in oncology: therapeutic opportunities for the treatment of brain tumours?

…, W Boogerd, I Thuis, JH Beijnen, O van Tellingen - Cancer treatment …, 2004 - Elsevier
Systemically administered chemotherapy is not very effective in the treatment of primary or
metastatic brain tumours. An important reason for this low efficacy is insufficient drug delivery …

[HTML][HTML] Concerns about anti-angiogenic treatment in patients with glioblastoma multiforme

JJC Verhoeff, O Van Tellingen, A Claes, LJA Stalpers… - BMC cancer, 2009 - Springer
Background The relevance of angiogenesis inhibition in the treatment of glioblastoma
multiforme (GBM) should be considered in the unique context of malignant brain tumours. …

Rapid esterase-sensitive breakdown of polysorbate 80 and its impact on the plasma pharmacokinetics of docetaxel and metabolites in mice

O Tellingen, JH Beijnen, J Verweij… - Clinical cancer …, 1999 - AACR
We have developed and validated an analytical methodology for the quantification of
docetaxel and its four major human oxidation metabolites in mouse plasma. We have used this …

Glycosylated extracellular vesicles released by glioblastoma cells are decorated by CCL18 allowing for cellular uptake via chemokine receptor CCR8

…, J van Rheenen, DM Pegtel, O Tellingen… - Journal of …, 2018 - Taylor & Francis
Cancer cells release extracellular vesicles (EVs) that contain functional biomolecules such
as RNA and proteins. EVs are transferred to recipient cancer cells and can promote tumour …

Normal viability and altered pharmacokinetics in mice lacking mdr1-type (drug-transporting) P-glycoproteins

…, H Spits, O Van Tellingen… - Proceedings of the …, 1997 - National Acad Sciences
The mdr1-type P-glycoproteins (P-gps) confer multidrug resistance to cancer cells by active
extrusion of a wide range of drugs from the cell. To study their physiological roles, we have …

Limited oral bioavailability and active epithelial excretion of paclitaxel (Taxol) caused by P-glycoprotein in the intestine

…, JH Beijnen, O Van Tellingen - Proceedings of the …, 1997 - National Acad Sciences
In mice, the mdr1a and mdr1b genes encode drug-transporting proteins that can cause
multidrug resistance in tumor cells by lowering intracellular drug levels. These P-glycoproteins …

Potent and Specific Inhibition of the Breast Cancer Resistance Protein Multidrug Transporter in Vitro and in Mouse Intestine by a Novel Analogue of Fumitremorgin C

…, JM Lakhai, M Van Der Valk, O Van Tellingen… - Molecular cancer …, 2002 - AACR
Inhibitors of the breast cancer resistance protein (BCRP/ABCG2) multidrug transporter are of
interest as chemosensitizers for clinical drug resistance, for improving the pharmacokinetics …

Role of glutathione in the export of compounds from cells by the multidrug-resistance-associated protein.

…, J Lankelma, O vAN Tellingen… - Proceedings of the …, 1995 - National Acad Sciences
Multidrug-resistance-associated protein (MRP) is a plasma membrane glycoprotein that can
confer multidrug resistance (MDR) by lowering intracellular drug concentration. Here we …

The Effect of Bcrp1 (Abcg2) on the In vivo Pharmacokinetics and Brain Penetration of Imatinib Mesylate (Gleevec): Implications for the Use of Breast Cancer …

…, D Pluim, G Cipriani, P Wielinga, O van Tellingen… - Cancer research, 2005 - AACR
Imatinib mesylate (signal transduction inhibitor 571, Gleevec) is a potent and selective
tyrosine kinase inhibitor, which was shown to effectively inhibit platelet-derived growth factor–…