Literature DB >> 19122343

Genetic variations of the SLCO1B1 gene in the Chinese, Malay and Indian populations of Singapore.

Woon Fei Ho1, Seok Hwee Koo, Jie Yin Yee, Edmund Jon Deoon Lee.   

Abstract

OATP1B1 is a liver-specific transporter that mediates the uptake of various endogenous and exogenous compounds including many clinically used drugs from blood into hepatocytes. This study aims to identify genetic variations of SLCO1B1 gene in three distinct ethnic groups of the Singaporean population (n=288). The coding region of the gene encoding the transporter protein was screened for genetic variations in the study population by denaturing high-performance liquid chromatography and DNA sequencing. Twenty-five genetic variations of SLCO1B1, including 10 novel ones, were found: 13 in the coding exons (9 nonsynonymous and 4 synonymous variations), 6 in the introns, and 6 in the 3' untranslated region. Four novel nonsynonymous variations: 633A>G (Ile211Met), 875C>T (Ala292Val), 1837T>C (Cys613Arg), and 1877T>A (Leu626Stop) were detected as heterozygotes. Among the novel nonsynonymous variations, 633A>G, 1837T>C, and 1877T>A were predicted to be functionally significant. These data would provide fundamental and useful information for pharmacogenetic studies on drugs that are substrates of OATP1B1 in Asians.

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Year:  2008        PMID: 19122343     DOI: 10.2133/dmpk.23.476

Source DB:  PubMed          Journal:  Drug Metab Pharmacokinet        ISSN: 1347-4367            Impact factor:   3.614


  7 in total

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3.  Genetic Variations and Frequencies of the Two Functional Single Nucleotide Polymorphisms of SLCO1B1 in the Thai Population.

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Journal:  Front Pharmacol       Date:  2020-06-05       Impact factor: 5.810

4.  Prevalence of pharmacogenomic variants in 100 pharmacogenes among Southeast Asian populations under the collaboration of the Southeast Asian Pharmacogenomics Research Network (SEAPharm).

Authors:  Chakkaphan Runcharoen; Koya Fukunaga; Insee Sensorn; Nareenart Iemwimangsa; Sommon Klumsathian; Hang Tong; Nam Sy Vo; Ly Le; Tin Maung Hlaing; Myo Thant; Shamsul Mohd Zain; Zahurin Mohamed; Yuh-Fen Pung; Francis Capule; Jose Nevado; Catherine Lynn Silao; Zeina N Al-Mahayri; Bassam R Ali; Rika Yuliwulandari; Kinasih Prayuni; Hilyatuz Zahroh; Dzul Azri Mohamed Noor; Phonepadith Xangsayarath; Dalouny Xayavong; Sengchanh Kounnavong; Somphou Sayasone; Zoe Kordou; Ioannis Liopetas; Athina Tsikrika; Evangelia-Eirini Tsermpini; Maria Koromina; Christina Mitropoulou; George P Patrinos; Aumpika Kesornsit; Angkana Charoenyingwattana; Sukanya Wattanapokayakit; Surakameth Mahasirimongkol; Taisei Mushiroda; Wasun Chantratita
Journal:  Hum Genome Var       Date:  2021-02-04

Review 5.  Genetic factors affecting statin concentrations and subsequent myopathy: a HuGENet systematic review.

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Journal:  Genet Med       Date:  2014-05-08       Impact factor: 8.822

6.  Polymorphic variants of SLCO1B1 in neonatal hyperbilirubinemia in China.

Authors:  Jiebo Liu; Jun Long; Shaofang Zhang; Xiaoyan Fang; Yuyuan Luo
Journal:  Ital J Pediatr       Date:  2013-08-12       Impact factor: 2.638

7.  Genetics is a major determinant of expression of the human hepatic uptake transporter OATP1B1, but not of OATP1B3 and OATP2B1.

Authors:  Anne T Nies; Mikko Niemi; Oliver Burk; Stefan Winter; Ulrich M Zanger; Bruno Stieger; Matthias Schwab; Elke Schaeffeler
Journal:  Genome Med       Date:  2013-01-11       Impact factor: 11.117

  7 in total

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