نتایج جستجو برای: ugt1a1 gene

تعداد نتایج: 1141874  

Journal: :Clinical chemistry 2010
Jing-Ping Lin Libor Vitek Harvey A Schwertner

BACKGROUND Serum bilirubin has been consistently shown to be inversely related to cardiovascular disease (CVD). Recent studies showed serum bilirubin to be associated with CVD-related factors such as diabetes, metabolic syndrome, and body mass index. Although the association of serum bilirubin with CVD has been found in both retrospective and prospective studies, less information is available o...

Journal: :Journal of Clinical and Experimental Hepatology 2016

Journal: :Blood cells, molecules & diseases 2012
Carina Rodrigues Emília Vieira Rosário Santos João de Carvalho Alice Santos-Silva Elísio Costa Elsa Bronze-da-Rocha

The Gilbert syndrome is a benign form of unconjugated hyperbilirubinemia, mainly associated with alterations in UGT1A1 gene. This work investigated the effect of UGT1A1 variants on total bilirubin levels in Gilbert patients (n=45) and healthy controls (n=161). Total bilirubin levels were determined using a colorimetric method; molecular analysis of exons 1-5 and two UGT1A1 promoter regions were...

2007
Andrew L. Hong Dezheng Huo Hee-Jin Kim Qun Niu Donna L. Fackenthal Shelly A. Cummings Esther M. John Dee W. West Alice S. Whittemore Soma Das Olufunmilayo I. Olopade

Objectives: To investigate variations in UGT1A1 polymorphisms and haplotypes among African American and Caucasian women and to assess whether variants other than UGT1A1*28 are associated with total serum bilirubin levels. Methods: The (TA)n repeats and 14 single nucleotide polymorphisms (SNPs) in the UGT1A1 gene were genotyped in 335 African Americans and 181 Caucasians. Total serum bilirubin l...

2017
Marcelo Moreira Tavares de Souza Victor Van Vaisberg Rodrigo Martins Abreu Aline Siqueira Ferreira Camila daSilvaFerreira Paulo Dominguez Nasser Helena Scavone Paschoale Flair José Carrilho Suzane Kioko Ono

Gilbert syndrome (GS) is a frequent benign clinical condition, marked by intermittent unconjugated hyperbilirubinemia, mostly due to the polymorphism uridine diphosphate-glucuronosyltransferase 1A1*28 (UGT1A1*28). Hyperbilirubinemia has been reported in a GS patient undergoing hepatitis C treatment, and other UGT isoforms polymorphisms have been linked to worse outcomes in viral hepatitis. Yet,...

2012
Cody J. Peer Tristan M. Sissung AeRang Kim Lokesh Jain Sukyung Woo Erin R. Gardner C. Tyler Kirkland Sarah M. Troutman Bevin C. English Emily D. Richardson Joel Federspiel David Venzon Elise Kohn Shivaani Kummar Robert Yarchoan Giuseppe Giaccone William D. Figg

Purpose: Several case reports suggest sorafenib exposure and sorafenib-induced hyperbilirubinemiamay be related to a (TA)5/6/7 repeat polymorphism in UGT1A1 28 (UGT, uridine glucuronosyl transferase). We hypothesized that sorafenib inhibits UGT1A1 and individuals carrying UGT1A1 28 and/or UGT1A9 variants experience greater sorafenib exposure and greater increase in sorafenib-induced plasma bili...

Journal: :Drug metabolism and pharmacokinetics 2014
Maiko Abumiya Naoto Takahashi Takenori Niioka Yoshihiro Kameoka Naohito Fujishima Hiroyuki Tagawa Kenichi Sawada Masatomo Miura

Nilotinib potently inhibits human uridine diphosphate-glucuronosyltransferase (UGT1A1) activity, causing hyperbilirubinemia. We investigated the influence of UGT1A1 polymorphisms and nilotinib plasma trough concentrations (C0) on nilotinib-induced hyperbilirubinemia in 34 Japanese patients with chronic myeloid leukemia (CML). The proportion of patients with hyperbilirubinemia was significantly ...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2009
Ye Li David Buckley Shuang Wang Curtis D Klaassen Xiao-bo Zhong

Transcription of UDP-glucuronosyltransferase (UGT) 1A1 is regulated by the transcription factors, constitutive androstane receptor (CAR), pregnane X receptor (PXR), glucocorticoid receptor (GR), hepatocyte nuclear factor (HNF) 1 alpha, and HNF4 alpha. The purpose of this study was to determine whether the genetic polymorphisms in the RNA polymerase II core promoter and the upstream phenobarbita...

Journal: :Molecules 2017
Ying Xie Sonia R Miranda Janelle M Hoskins Roy L Hawke

Silymarin is the most commonly used herbal medicine by patients with chronic liver disease. Silymarin flavonolignans undergo rapid first-pass metabolism primarily by glucuronidation. The aims of this investigation were: (1) to determine the association of UGT1A1*28 polymorphism with the area under the plasma concentration-time curves (AUCs) for silybin A (SA) and silybin B (SB); (2) to evaluate...

Journal: :Molecules 2016
Yu Fen Zheng Jee Sun Min Doyun Kim Jung Bae Park Sung-Wook Choi Eun Seong Lee Kun Na Soo Kyung Bae

Despite the widespread use of the five major xanthophylls astaxanthin, β-cryptoxanthin, canthaxanthin, lutein, and zeaxanthin as dietary supplements, there have been no studies regarding their inhibitory effects on hepatic UDP-glucuronosyltransferases (UGTs). Here, we evaluated the inhibitory potential of these xanthophylls on the seven major human hepatic UGTs (UGT1A1, UGT1A3, UGT1A4, UGT1A6, ...

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