Search Results - "Meijerman, I."
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Keeping pace in the age of innovation: The perspective of Dutch pharmaceutical science students on the position of machine learning training in an undergraduate curriculum
Published in Currents in pharmacy teaching and learning (01-02-2025)“…Over the years, approaches of the pharmaceutical industry to discover and develop drugs have changed rapidly due to new scientific trends. Among others, they…”
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The role of nuclear receptors in pharmacokinetic drug–drug interactions in oncology
Published in Cancer treatment reviews (01-06-2007)“…Summary Drug–drug interactions can have a major impact on treatment outcome in cancer patients. These patients are at high risk of such interactions, because…”
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Effect of Chinese herbs on CYP3A4 activity and expression in vitro
Published in Journal of ethnopharmacology (16-09-2013)“…Traditional Chinese Medicine (TCM) has become more popular among cancer patients in the Western world, who often use Chinese herbs as adjuvant therapy to…”
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Nuclear receptor mediated induction of cytochrome P450 3A4 by anticancer drugs: a key role for the pregnane X receptor
Published in Cancer chemotherapy and pharmacology (01-06-2009)“…Purpose Induction of cytochrome P450 (CYP) 3A4, an enzyme that is involved in the biotransformation of more than 50% of all drugs, by xenobiotics is an…”
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PXR-mediated P-glycoprotein induction by small molecule tyrosine kinase inhibitors
Published in European journal of pharmaceutical sciences (12-03-2013)“…In this paper, we demonstrate that pregnane X receptor (PXR)-mediated induction of P-glycoprotein (PGP) is an important mechanism by which tyrosine kinase…”
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Germline TYMS genotype is highly predictive in patients with metastatic gastrointestinal malignancies receiving capecitabine-based chemotherapy
Published in Cancer chemotherapy and pharmacology (01-04-2015)“…Purpose This work was initiated to extend data on the effect of pharmacogenetics and chemotherapy pharmacokinetics (PK) on clinical outcome in patients with…”
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PXR-mediated induction of P-glycoprotein by anticancer drugs in a human colon adenocarcinoma-derived cell line
Published in Cancer chemotherapy and pharmacology (01-09-2010)“…Purpose The development of multidrug resistance (MDR) is one of the major limitations in the treatment of cancer. Induction of P-glycoprotein (Pgp) has been…”
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Comparison of Two Immortalized Human Cell Lines to Study Nuclear Receptor-Mediated CYP3A4 Induction
Published in Drug metabolism and disposition (01-06-2008)“…Since CYP3A4 is responsible for the biotransformation of over 50% of all clinically used drugs, induction results in an increased clearance of many…”
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Development and validation of a LC-MS/MS method for the in vitro analysis of 1-hydroxymidazolam in human liver microsomes: application for determining CYP3A4 inhibition in complex matrix mixtures
Published in Biomedical chromatography (01-09-2013)“…ABSTRACT Complementary and alternative medicines (CAM) can affect the pharmacokinetics of anticancer drugs by interacting with the metabolizing enzyme…”
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Effects of cytochrome P450 2C9 polymorphisms on phenprocoumon anticoagulation status
Published in Clinical pharmacology and therapeutics (01-11-2004)“…Objective Our objective was to assess whether there is an association between the presence of allelic variants of the gene for cytochrome P450 (CYP) 2C9 and…”
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Lethal toxicity of uracil/tegafur in the treatment of sigmoid carcinoma
Published in Annals of oncology (01-03-2007)Get full text
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Pharmacogenetic screening for polymorphisms in drug-metabolizing enzymes and drug transporters in a Dutch population
Published in Molecular diagnosis & therapy (01-01-2006)“…A possible explanation for the wide interindividual variability in toxicity and efficacy of drug therapy is variation in genes encoding drug-metabolizing…”
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An update on in vitro test methods in human hepatic drug biotransformation research: pros and cons
Published in Toxicology and applied pharmacology (15-06-2003)“…The liver is the predominant organ in which biotransformation of foreign compounds takes place, although other organs may also be involved in drug…”
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1577PGERMLINE TYMS GENOTYPE IS HIGHLY PREDICTIVE IN PATIENTS WITH ADVANCED COLORECTAL AND GASTROESOPHAGEAL CANCER INDEPENDENT OF FLUOROPYRIMIDINE PHARMACOLOGY: RESULTS FROM TWO PROSPECTIVE TRANSLATIONAL STUDIES
Published in Annals of oncology (01-09-2014)“…Abstract Aim: Germline gene polymorphisms may impact clinical outcome in patients with gastrointestinal malignancies, but there are no data on the interaction…”
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Validation of in vitro cell models used in drug metabolism and transport studies; genotyping of cytochrome P450, phase II enzymes and drug transporter polymorphisms in the human hepatoma (HepG2), ovarian carcinoma (IGROV-1) and colon carcinoma (CaCo-2, LS180) cell lines
Published in Toxicology and applied pharmacology (15-02-2006)“…Human cell lines are often used for in vitro biotransformation and transport studies of drugs. In vivo, genetic polymorphisms have been identified in…”
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MDMA (drug)–drug interactions influence CYP3A4 expression via PXR-mediator
Published in Toxicology letters (17-07-2010)Get full text
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Screening for polymorphisms in the PXR gene in a Dutch population
Published in European journal of clinical pharmacology (01-05-2006)“…Cytochrome P450 3A4 (CYP3A4) is involved in the metabolism of over 50% of all drugs currently in use. However, CYP3A4 expression shows a large inter-individual…”
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In-vitro cytotoxicity of ET-743 (Trabectedin, Yondelis), a marine anti-cancer drug, in the Hep G2 cell line: influence of cytochrome P450 and phase II inhibition, and cytochrome P450 induction
Published in Anti-cancer drugs (01-10-2005)“…ET-743 is a marine anti-cancer drug and is currently in phase I trials in which the effect of combination therapies will be investigated. Its dose-limiting…”
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Prevention of cycloheximide-induced apoptosis in hepatocytes by adenosine and by caspase inhibitors
Published in Biochemical pharmacology (15-12-1999)“…The mechanism by which cycloheximide induces apoptosis in isolated rat hepatocytes was studied. Cycloheximide (1–300 μM) induced apoptosis within 3–4 hr in the…”
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