دورية أكاديمية

SNPs Sets in Codifying Genes for Xenobiotics-Processing Enzymes Are Associated with COPD Secondary to Biomass-Burning Smoke

التفاصيل البيبلوغرافية
العنوان: SNPs Sets in Codifying Genes for Xenobiotics-Processing Enzymes Are Associated with COPD Secondary to Biomass-Burning Smoke
المؤلفون: Enrique Ambrocio-Ortiz, Gloria Pérez-Rubio, Alejandra Ramírez-Venegas, Rafael de Jesús Hernández-Zenteno, Juan Carlos Fernández-López, María Elena Ramírez-Díaz, Filiberto Cruz-Vicente, María de Lourdes Martínez-Gómez, Raúl Sansores, Julia Pérez-Ramos, Ramcés Falfán-Valencia
المصدر: Current Issues in Molecular Biology, Vol 45, Iss 2, Pp 799-819 (2023)
بيانات النشر: MDPI AG, 2023.
سنة النشر: 2023
المجموعة: LCC:Biology (General)
مصطلحات موضوعية: chronic obstructive pulmonary disease, toxicity, indoor pollution, microarray analysis, genome-wide association study, Biology (General), QH301-705.5
الوصف: Chronic obstructive pulmonary disease (COPD) is the third leading cause of death worldwide; the main risk factors associated with the suffering are tobacco smoking (TS) and chronic exposure to biomass-burning smoke (BBS). Different biological pathways have been associated with COPD, especially xenobiotic or drug metabolism enzymes. This research aims to identify single nucleotide polymorphisms (SNPs) profiles associated with COPD from two expositional sources: tobacco smoking and BBS. One thousand-five hundred Mexican mestizo subjects were included in the study and divided into those exposed to biomass-burning smoke and smokers. Genome-wide exome genotyping was carried out using Infinium Exome-24 kit arrays v. 1.2. Data quality control was conducted using PLINK 1.07. For clinical and demographic data analysis, Rstudio was used. Eight SNPs were found associated with COPD secondary to TS and seven SNPs were conserved when data were analyzed by genotype. When haplotype analyses were carried out, five blocks were predicted. In COPD secondary to BBS, 24 SNPs in MGST3 and CYP family genes were associated. Seven blocks of haplotypes were associated with COPD-BBS. SNPs in the ARNT2 and CYP46A1 genes are associated with COPD secondary to TS, while in the BBS comparison, SNPs in CYP2C8, CYP2C9, MGST3, and MGST1 genes were associated with increased COPD risk.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1467-3045
1467-3037
Relation: https://www.mdpi.com/1467-3045/45/2/53; https://doaj.org/toc/1467-3037; https://doaj.org/toc/1467-3045
DOI: 10.3390/cimb45020053
URL الوصول: https://doaj.org/article/b3958effa7c246bba04eb47799c80d1c
رقم الأكسشن: edsdoj.b3958effa7c246bba04eb47799c80d1c
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:14673045
14673037
DOI:10.3390/cimb45020053