نتایج جستجو برای: cyp3a4 promoter

تعداد نتایج: 92660  

Journal: :Biological & pharmaceutical bulletin 2013
Miwa Uesugi Mio Hosokawa Haruka Shinke Emina Hashimoto Tamotsu Takahashi Tomoki Kawai Kazuo Matsubara Kohei Ogawa Yasuhiro Fujimoto Shinya Okamoto Toshimi Kaido Shinji Uemoto Satohiro Masuda

Association between cytochrome P450 (CYP) 3A4*1G genotype of donors (n=412) and/or recipients (n=410), and the pharmacokinetics of tacrolimus and the risk of acute cellular rejection was examined in Japanese living-donor liver transplant patients between 2004 and 2011. The concentration/dose (C/D) ratio of tacrolimus in patients carrying graft liver with CYP3A4*1/*1 was significantly higher dur...

Journal: :Molecular cancer therapeutics 2016
Meiyan Sun Qunshu Zhang Xiaoyu Yang Steven Y Qian Bin Guo

Cytochrome P450 enzyme CYP3A4 is an important drug-metabolizing enzyme, and high levels of tumoral expression of CYP3A4 are linked to drug resistance. We investigated the function of vitamin D-regulated miR-627 in intratumoral CYP3A4 suppression and its role in enhancing the efficacy of chemotherapy. We found that miR-627 targets CYP3A4 and suppresses CYP3A4 expression in colon cancer cell line...

2014
Joseph P. Kitzmiller Jasmine A. Luzum Damiano Baldassarre Ronald M. Krauss Marisa W. Medina

OBJECTIVE Simvastatin is primarily metabolized by CYP3A4. A combined CYP3A4/5 genotype classification, combining the decrease-of-function CYP3A4*22 and the loss-of-function CYP3A5*3, has recently been reported. We aim to determine whether CYP3A4*22 and CYP3A5*3 alleles are associated with increased plasma concentrations of simvastatin lactone (SV) and simvastatin acid (SVA). This is the first r...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2005
Antonius E van Herwaarden Johan W Smit Rolf W Sparidans Els Wagenaar Cornelia M M van der Kruijssen Jan H M Schellens Jos H Beijnen Alfred H Schinkel

Cytochrome P450 3A4 (CYP3A4) is a major determinant of the metabolism of many drugs, including important anticancer drugs, with sometimes profound impact on therapeutic efficacy and toxic side effects. To study in vivo CYP3A(4) functions, we have generated and characterized transgenic mice with functional expression of human CYP3A4 cDNA in the liver. Two transgenic lines displayed substantial, ...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2009
Gry Vibeke Bakken Ida Rudberg Hege Christensen Espen Molden Helge Refsum Monica Hermann

The antipsychotic drug quetiapine is extensively metabolized by CYP3A4, but little is known about the possible influence of the polymorphic enzyme CYP3A5. This in vitro study investigated the relative importance of CYP3A4 and CYP3A5 in the metabolism of quetiapine and compared the metabolic pattern by the two enzymes, in the presence or absence of cytochrome b(5). Intrinsic clearance (CL(int)) ...

Journal: :The Biochemical journal 2010
Yassar Farooq Gordon C K Roberts

We have incorporated CYP3A4 (cytochrome P450 3A4) and CPR (NADPH-cytochrome P450 reductase) into liposomes with a high lipid/protein ratio by an improved method. In the purified proteoliposomes, CYP3A4 binds testosterone with Kd (app)=36±6 μM and Hill coefficient=1.5±0.3, and 75±4% of the CYP3A4 can be reduced by NADPH in the presence of testosterone. Transfer of the first electron from CPR to ...

2016
Kun Liu Shuo Gu Xuzhong Liu Qing Sun Yunyan Wang Junsong Meng Zongyuan Xu

Purpose: The mutation frequency of the CYP3A4 *18B genetic polymorphism is relatively high in Asian populations. The influence of this polymorphism on the pharmacokinetics of cyclosporine A (CsA) is controversial. We investigated the association between the CYP3A4 *18B polymorphism and CsA pharmacokinetics in Chinese renaltransplant recipients. Methods: A literature search was conducted in PubM...

Journal: :Current topics in medicinal chemistry 2014
Irina F Sevrioukova Thomas L Poulos

Inactivation of human drug-metabolizing cytochrome P450 3A4 (CYP3A4) could lead to serious adverse events such as drug-drug interactions and toxicity. However, when properly controlled, CYP3A4 inhibition may be beneficial as it can improve clinical efficacy of co-administered therapeutics that otherwise are quickly metabolized by CYP3A4. Currently, the CYP3A4 inhibitor ritonavir and its derivat...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2002
Gang Luo Mark Cunningham Sean Kim Tim Burn Jianrong Lin Michael Sinz Geraldine Hamilton Christopher Rizzo Summer Jolley Darryl Gilbert April Downey Daniel Mudra Richard Graham Kathy Carroll Jindong Xie Ajay Madan Andrew Parkinson Dave Christ Bernard Selling Edward LeCluyse Liang-Shang Gan

Induction of cytochrome P450 3A4 (CYP3A4) is determined typically by employing primary culture of human hepatocytes and measuring CYP3A4 mRNA, protein and microsomal activity. Recently a pregnane X receptor (PXR) reporter gene assay was established to screen CYP3A4 inducers. To evaluate results from the PXR reporter gene assay with those from the aforementioned conventional assays, 14 drugs wer...

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