نتایج جستجو برای: ژن ugt1a1
تعداد نتایج: 16921 فیلتر نتایج به سال:
سندرم کریگلر- نجار نوع 1، یک بیماری نادر اتوزومی مغلوب با شیوع 1 در یک میلیون نوزاد می باشد و با افزایش بیلی روبین غیر کنژوگه و غیر همولیتیک شناخته می شود. این سندرم طی دوره ی نوزادی با زردی زودرس و شدید آشکار می گردد. بیماری در اثر جهش در ژنugt1a1 که باعث فقدان تقریباً کامل فعالیت آنزیم ugt1a1 و در نتیجه عدم ترکیب بیلی روبین با گلوکورونیک اسید می گردد، ایجاد می شود. لوکوس ugt1a1 بر روی کروموزوم...
OBJECTIVE To assess the prevalence of UGT1A1*28 and UGT1A1*60 polymorphisms of UGT1A1 gene and their association with hyperbilirubinemia. STUDY DESIGN The study was performed at a single centre - at the Department of Obstetrics of the Medical University of Gdansk in Poland. DNA was isolated from Guthrie cards of 171 infants. Only full term newborns (gestational age 38-42 weeks) were included ...
Of the hepatic UDP-glucuronosyltransferases (UGTs), only UGT1A1 and UGT1A9 exhibit activity against benzo(a)pyrene-trans-7R,8R-dihydrodiol [BPD(-)], precursor to the highly mutagenic anti-(+)-benzo(a)pyrene-7R,8S-dihydrodiol-9S,10R-epoxide. The UGT1A1*28 allelic variant contains an additional (TA) dinucleotide repeat in the "TATAA" box [(TA)(6)>(TA)(7)] of the UGT1A1 promoter that has been link...
PURPOSE Irinotecan is used in the first-line treatment of metastatic colorectal cancer. The UGT1A1-metabolizing enzyme, expressed in liver and colon, is primarily involved in the inactivation of its active metabolite 7-ethyl-10-hydroxycamptothecin (SN-38). Herein, we explored the role of DNA methylation in the silencing of UGT1A1 gene expression in colon cancer and its influence on cellular SN-...
UDP-glucuronosyltransferase 1A1 (UGT1A1) is a vital metabolic enzyme responsible for the clearance of endogenous substances and drugs. Hitherto, development fluorescent probes UGTs was severely restricted due to poor isoform selectivity on–off or blue-shifted fluorescence response. Herein, we established novel “molecular-splicing” strategy construct highly selective near-infrared (NIR) probe, H...
Irinotecan unexpectedly causes severe toxicity of leukopenia or diarrhea. Irinotecan is metabolized to form active SN-38, which is further conjugated and detoxified by UDP-glucuronosyltransferase (UGT) 1A1 enzyme. Genetic polymorphisms of the UGT1A1 would affect an interindividual variation of the toxicity by irinotecan via the alternation of bioavailability of SN-38. In this case-control study...
BACKGROUND & OBJECTIVES Genetic polymorphisms of uridine diphosphate glucuronyltransferase 1A1 (UGT1A1) have been associated with a wide variation of responses among patients prescribed with irinotecan. Lack of this enzyme is known to be associated with a high incidence of severe toxicity. The objective of this study was to investigate the prevalence of three different variants of UGT1A1 (UGT1A...
Uridine diphosphate glucuronosyltransferase 1A (UGT1A1), which affects irinotecan metabolism, has been associated with severe adverse reactions in patients with cancer treated with irinotecan. However, neither large-scale analysis of the distribution of UGT1A1 polymorphisms, nor standardized assessment of how UGT1A1 polymorphisms affect irinotecan treatment has been performed in China. The aim ...
The objective of this study was to determine allele frequency and genotyping of UGT1A1 polymorphisms (UGT1A1*28 and UGT1A1*6) in Thai colorectal cancer patients who received irinotecan treatment and develop pyrosequencing technique for UGT1A1 genetic polymorphisms detection. The Ninety-one patients entered the study. The results showed the allele frequencies for UGT1A1 genetic polymorphisms wer...
BACKGROUND Uridine 5'-diphospho-glucuronosyltransferase 1A1 (UGT1A1*27) is known to impair the effect of UGT in basic research; however, little clinical investigation has been conducted. To evaluate the effect of the UGT1A1*27 polymorphism in irinotecan therapy, we conducted a prospective study. METHODS Eligibility criteria included: lung cancer patients; scheduled irinotecan therapy doses of...
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