Search Results - "Zanger, Ulrich M"
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Pharmacogenetics of cytochrome P450 2B6 (CYP2B6): advances on polymorphisms, mechanisms, and clinical relevance
Published in Frontiers in genetics (2013)“…Cytochrome P450 2B6 (CYP2B6) belongs to the minor drug metabolizing P450s in human liver. Expression is highly variable both between individuals and within…”
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MiR-155 and other microRNAs downregulate drug metabolizing cytochromes P450 in inflammation
Published in Biochemical pharmacology (01-01-2020)“…[Display omitted] In conditions of acute and chronic inflammation hepatic detoxification capacity is severely impaired due to coordinated downregulation of…”
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Pharmacogenomics of Cytochrome P450 3A4: Recent Progress Toward the "Missing Heritability" Problem
Published in Frontiers in genetics (2013)“…CYP3A4 is the most important drug metabolizing enzyme in adult humans because of its prominent expression in liver and gut and because of its broad substrate…”
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Functional pharmacogenetics/genomics of human cytochromes P450 involved in drug biotransformation
Published in Analytical and bioanalytical chemistry (01-11-2008)“…We investigated the elimination routes for the 200 drugs that are sold most often by prescription count in the United States. The majority (78%) of the…”
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Tri‐Allelic Haplotypes Determine and Differentiate Functionally Normal Allele CYP2D62 and Impaired Allele CYP2D641
Published in Clinical pharmacology and therapeutics (01-05-2021)“…CYP2D6 metabolizes 20–25% of all clinically used drugs and its complex genetic polymorphism is a major determinant of drug safety and efficacy. We investigated…”
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Breast Cancer Treatment Outcome With Adjuvant Tamoxifen Relative to Patient CYP2D6 and CYP2C19 Genotypes
Published in Journal of clinical oncology (20-11-2007)“…The clinical outcome of tamoxifen-treated breast cancer patients may be influenced by the activity of cytochrome P450 enzymes that catalyze the formation of…”
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Expression of organic cation transporters OCT1 (SLC22A1) and OCT3 (SLC22A3) is affected by genetic factors and cholestasis in human liver
Published in Hepatology (Baltimore, Md.) (01-10-2009)“…An important function of hepatocytes is the biotransformation and elimination of various drugs, many of which are organic cations and are taken up by organic…”
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A systematic comparison of the impact of inflammatory signaling on absorption, distribution, metabolism, and excretion gene expression and activity in primary human hepatocytes and HepaRG cells
Published in Drug metabolism and disposition (01-02-2015)“…Inflammatory processes are associated with compromised metabolism and elimination of drugs in the liver, largely mediated by proinflammatory cytokines, such as…”
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Inflammation-associated microRNA-130b down-regulates cytochrome P450 activities and directly targets CYP2C9
Published in Drug metabolism and disposition (01-06-2015)“…Expression of genes involved in absorption, distribution, metabolism, and excretion (ADME) of drugs is impaired in pathophysiologic conditions such as…”
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Progesterone receptor membrane component 1 regulates lipid homeostasis and drives oncogenic signaling resulting in breast cancer progression
Published in Breast cancer research : BCR (13-07-2020)“…PGRMC1 (progesterone receptor membrane component 1) is a highly conserved heme binding protein, which is overexpressed especially in hormone receptor-positive…”
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Role of Genetic and Nongenetic Factors for Fluorouracil Treatment-Related Severe Toxicity: A Prospective Clinical Trial by the German 5-FU Toxicity Study Group
Published in Journal of clinical oncology (01-05-2008)“…To assess the predictive value of polymorphisms in dihydropyrimidine dehydrogenase (DPYD ), thymidylate synthase (TYMS ), and methylene tetrahydrofolate…”
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Differential effects on human cytochromes P450 by CRISPR/Cas9-induced genetic knockout of cytochrome P450 reductase and cytochrome b5 in HepaRG cells
Published in Scientific reports (13-01-2021)“…HepaRG cells are increasingly accepted as model for human drug metabolism and other hepatic functions. We used lentiviral transduction of undifferentiated…”
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Polycyclic Aromatic Hydrocarbons Activate the Aryl Hydrocarbon Receptor and the Constitutive Androstane Receptor to Regulate Xenobiotic Metabolism in Human Liver Cells
Published in International journal of molecular sciences (31-12-2020)“…Polycyclic aromatic hydrocarbons (PAHs) are environmental pollutants produced by incomplete combustion of organic matter. They induce their own metabolism by…”
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Transcriptional profiling of human liver identifies sex-biased genes associated with polygenic dyslipidemia and coronary artery disease
Published in PloS one (12-08-2011)“…Sex-differences in human liver gene expression were characterized on a genome-wide scale using a large liver sample collection, allowing for detection of small…”
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Cytochrome P450 2D6: overview and update on pharmacology, genetics, biochemistry
Published in Naunyn-Schmiedeberg's archives of pharmacology (01-01-2004)“…Of about one dozen human P450 s that catalyze biotransformations of xenobiotics, CYP2D6 is one of the more important ones based on the number of its drug…”
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Role of ABC Transporters in Fluoropyrimidine-Based Chemotherapy Response
Published in ABC Transporters and Cancer (2015)“…Since over 50 years, 5-fluorouracil (5-FU) is in use as backbone of chemotherapy treatment regimens for a wide range of cancers including colon, breast, and…”
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Cytochrome P450 enzymes in drug metabolism: Regulation of gene expression, enzyme activities, and impact of genetic variation
Published in Pharmacology & therapeutics (Oxford) (01-04-2013)“…Cytochromes P450 (CYP) are a major source of variability in drug pharmacokinetics and response. Of 57 putatively functional human CYPs only about a dozen…”
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18
Model-Based Characterization of Inflammatory Gene Expression Patterns of Activated Macrophages
Published in PLoS computational biology (01-07-2016)“…Macrophages are cells with remarkable plasticity. They integrate signals from their microenvironment leading to context-dependent polarization into classically…”
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Aberrant splicing caused by single nucleotide polymorphism c.516G>T [Q172H], a marker of CYP2B66, is responsible for decreased expression and activity of CYP2B6 in liver
Published in The Journal of pharmacology and experimental therapeutics (01-04-2008)“…CYP2B6 is a polymorphic human drug metabolizing cytochrome P450 with clinical relevance for several drug substrates including cyclophosphamide, bupropion, and…”
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Direct transcriptional regulation of human hepatic cytochrome P450 3A4 (CYP3A4) by peroxisome proliferator-activated receptor alpha (PPARα)
Published in Molecular pharmacology (01-03-2013)“…The nuclear receptor peroxisome proliferator-activated receptor (PPAR)α is known primarily as a regulator of fatty acid metabolism, energy balance, and…”
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