Literature DB >> 34383246

Population diversity of three variants of the SLC47A2 gene (MATE2-K transporter) in Mexican Mestizos and Native Americans.

Alma Faviola Favela-Mendoza1, Ingrid Fricke-Galindo2, Wendy Fernanda Cuevas-Sánchez3, José Alonso Aguilar-Velázquez3, Gabriela Martínez-Cortés3, Héctor Rangel-Villalobos4.   

Abstract

BACKGROUND: MATE2-K is an efflux transporter protein of organic cation expressed mainly in the kidney and encoded by the SLC47A2 gene. Different variants of this gene have shown an impact on the pharmacokinetics of various drugs, including metformin, which represents one of the most widely used drugs in treating type 2 diabetes. The SLC47A2 gene variants have been scarcely studied in Mexican populations, especially in Native American groups. For this reason, we analyzed the distribution of the variants rs12943590, rs35263947, and rs9900497 within the SLC47A2 gene in 173 Native Americans (Tarahumara, Huichol, Maya, Puerépecha) and 182 Mestizos (admixed) individuals from Mexico. METHODS AND
RESULTS: Genotypes were determined through TaqMan probes (qPCR). The Hardy-Weinberg agreement was confirmed for all three SLC47A2 gene variants in all the Mexican populations analyzed. When worldwide populations were included for comparison purposes, for alleles and genotypes a relative interpopulation homogeneity was observed for rs35263947 (T allele; range 23.3-51.1%) and rs9900497 (T allele; range 18.6-40.9%). Conversely, heterogeneity was evident for rs12943590 (A allele, range 22.1-59.1%), where the most differentiated population was the Huichol, with high frequencies of the risk genotype associated with decreased response to metformin treatment (A/A = 40.9%).
CONCLUSIONS: Although the SLC47A2 gene variants allow predicting favorable response to the metformin treatment in Mexican populations, the probable high frequency of ineffectiveness should be discarded in Huichols.
© 2021. The Author(s), under exclusive licence to Springer Nature B.V.

Entities:  

Keywords:  MATE2-K; Mestizos; Metformin; Mexico; Native Americans; SLC47A2

Mesh:

Substances:

Year:  2021        PMID: 34383246     DOI: 10.1007/s11033-021-06628-y

Source DB:  PubMed          Journal:  Mol Biol Rep        ISSN: 0301-4851            Impact factor:   2.316


  15 in total

1.  A common 5'-UTR variant in MATE2-K is associated with poor response to metformin.

Authors:  J H Choi; S W Yee; A H Ramirez; K M Morrissey; G H Jang; P J Joski; J A Mefford; S E Hesselson; A Schlessinger; G Jenkins; R A Castro; S J Johns; D Stryke; A Sali; T E Ferrin; J S Witte; P-Y Kwok; D M Roden; R A Wilke; C A McCarty; R L Davis; K M Giacomini
Journal:  Clin Pharmacol Ther       Date:  2011-09-28       Impact factor: 6.875

2.  Identification and functional characterization of novel nonsynonymous variants in the human multidrug and toxin extrusion 2-K.

Authors:  Kenta Nishimura; Ryosuke Ide; Takeshi Hirota; Kana Kawazu; Sho Kodama; Hiroaki Takesue; Ichiro Ieiri
Journal:  Drug Metab Dispos       Date:  2014-07-01       Impact factor: 3.922

3.  Lack of effect of the SLC47A1 and SLC47A2 gene polymorphisms on the glycemic response to metformin in type 2 diabetes mellitus patients.

Authors:  Gerard Marshall Raj; Jayanthi Mathaiyan; Mukta Wyawahare; Rekha Priyadarshini
Journal:  Drug Metab Pers Ther       Date:  2018-12-19

Review 4.  Structure and function of multidrug and toxin extrusion proteins (MATEs) and their relevance to drug therapy and personalized medicine.

Authors:  Anne T Nies; Katja Damme; Stephan Kruck; Elke Schaeffeler; Matthias Schwab
Journal:  Arch Toxicol       Date:  2016-05-10       Impact factor: 5.153

5.  Pharmacogenetic Evaluation of Metformin and Sulphonylurea Response in Mexican Mestizos with Type 2 Diabetes.

Authors:  Menjivar Marta; Katy Sánchez-Pozos; Joel Jaimes-Santoyo; Jazmin Monroy-Escutia; Carolina Rivera-Santiago; María de Los Ángeles Granados-Silvestre; María Guadalupe Ortiz-López
Journal:  Curr Drug Metab       Date:  2020       Impact factor: 3.731

Review 6.  Multidrug and toxin extrusion proteins (MATE/SLC47); role in pharmacokinetics.

Authors:  Frantisek Staud; Lukas Cerveny; Davoud Ahmadimoghaddam; Martina Ceckova
Journal:  Int J Biochem Cell Biol       Date:  2013-07-05       Impact factor: 5.085

7.  Influence of pharmacogenetic polymorphisms and demographic variables on metformin pharmacokinetics in an admixed Brazilian cohort.

Authors:  Ana Beatriz Santoro; Mariana Rodrigues Botton; Claudio José Struchiner; Guilherme Suarez-Kurtz
Journal:  Br J Clin Pharmacol       Date:  2018-02-26       Impact factor: 4.335

Review 8.  Multidrug and toxin extrusion family SLC47: physiological, pharmacokinetic and toxicokinetic importance of MATE1 and MATE2-K.

Authors:  Hideyuki Motohashi; Ken-ichi Inui
Journal:  Mol Aspects Med       Date:  2013 Apr-Jun

9.  The effect of novel promoter variants in MATE1 and MATE2 on the pharmacokinetics and pharmacodynamics of metformin.

Authors:  S L Stocker; K M Morrissey; S W Yee; R A Castro; L Xu; A Dahlin; A H Ramirez; D M Roden; R A Wilke; C A McCarty; R L Davis; C M Brett; K M Giacomini
Journal:  Clin Pharmacol Ther       Date:  2012-10-17       Impact factor: 6.875

10.  A global reference for human genetic variation.

Authors:  Adam Auton; Lisa D Brooks; Richard M Durbin; Erik P Garrison; Hyun Min Kang; Jan O Korbel; Jonathan L Marchini; Shane McCarthy; Gil A McVean; Gonçalo R Abecasis
Journal:  Nature       Date:  2015-10-01       Impact factor: 49.962

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