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Distribution of Lewis and Secretor polymorphisms and corresponding CA19‐9 antigen expression in a Chinese population

The Lewis (FUT3) and Secretor (FUT2) genes, corresponding to secretion of Lewis ABO (H) histo‐blood group antigen CA19‐9, are highly polymorphic with differences between populations. In this study, the FUT3 and FUT2 genes in 316 Chinese participants were sequenced to detect polymorphisms, and the as...

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Autores principales: Guo, Meng, Luo, Guopei, Lu, Renquan, Shi, Weizhong, Cheng, He, Lu, Yu, Jin, Kaizhou, Yang, Chao, Wang, Zhengshi, Long, Jiang, Xu, Jin, Ni, Quanxing, Liu, Chen, Yu, Xianjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5666394/
https://www.ncbi.nlm.nih.gov/pubmed/29123975
http://dx.doi.org/10.1002/2211-5463.12278
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author Guo, Meng
Luo, Guopei
Lu, Renquan
Shi, Weizhong
Cheng, He
Lu, Yu
Jin, Kaizhou
Yang, Chao
Wang, Zhengshi
Long, Jiang
Xu, Jin
Ni, Quanxing
Liu, Chen
Yu, Xianjun
author_facet Guo, Meng
Luo, Guopei
Lu, Renquan
Shi, Weizhong
Cheng, He
Lu, Yu
Jin, Kaizhou
Yang, Chao
Wang, Zhengshi
Long, Jiang
Xu, Jin
Ni, Quanxing
Liu, Chen
Yu, Xianjun
author_sort Guo, Meng
collection PubMed
description The Lewis (FUT3) and Secretor (FUT2) genes, corresponding to secretion of Lewis ABO (H) histo‐blood group antigen CA19‐9, are highly polymorphic with differences between populations. In this study, the FUT3 and FUT2 genes in 316 Chinese participants were sequenced to detect polymorphisms, and the associated CA19‐9 antigen secretion was also measured. In total, 14 genotypes of FUT3 and 10 genotypes of FUT2 were verified. Le/Le, Le/le (59,508) and Le/le (59) were the main genotypes of FUT3 with frequencies of 53.2%, 10.7% and 3.5%, respectively. Se/Se, Se/se (385) and se (385)/se (385) were the main genotypes of FUT2, with frequencies of 21.4%, 18.6% and 16.2%, respectively. The alleles le (1067) and le (508) were found extensively in the Chinese population, and the frequency of allele se (385) was shown to be higher than previously reported. Phenotype analysis revealed that 9.8% of individuals were the Lewis‐negative type and 22.5% were the secretor‐negative type. Combined phenotypes showed that 3.2% of participants were of ‘double‐negative’ phenotype (le, se) and 19.3% were of single dominant non‐secretor phenotype (Le, se). Serum Lewis antigen CA19‐9 levels were significantly different between subgroups and consistent with the defined phenotype. Our study revealed the unique distribution of Lewis and Secretor polymorphisms in a large Chinese population, and decoded the combined genotypes of the two CA19‐9‐related genes.
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spelling pubmed-56663942017-11-09 Distribution of Lewis and Secretor polymorphisms and corresponding CA19‐9 antigen expression in a Chinese population Guo, Meng Luo, Guopei Lu, Renquan Shi, Weizhong Cheng, He Lu, Yu Jin, Kaizhou Yang, Chao Wang, Zhengshi Long, Jiang Xu, Jin Ni, Quanxing Liu, Chen Yu, Xianjun FEBS Open Bio Research Articles The Lewis (FUT3) and Secretor (FUT2) genes, corresponding to secretion of Lewis ABO (H) histo‐blood group antigen CA19‐9, are highly polymorphic with differences between populations. In this study, the FUT3 and FUT2 genes in 316 Chinese participants were sequenced to detect polymorphisms, and the associated CA19‐9 antigen secretion was also measured. In total, 14 genotypes of FUT3 and 10 genotypes of FUT2 were verified. Le/Le, Le/le (59,508) and Le/le (59) were the main genotypes of FUT3 with frequencies of 53.2%, 10.7% and 3.5%, respectively. Se/Se, Se/se (385) and se (385)/se (385) were the main genotypes of FUT2, with frequencies of 21.4%, 18.6% and 16.2%, respectively. The alleles le (1067) and le (508) were found extensively in the Chinese population, and the frequency of allele se (385) was shown to be higher than previously reported. Phenotype analysis revealed that 9.8% of individuals were the Lewis‐negative type and 22.5% were the secretor‐negative type. Combined phenotypes showed that 3.2% of participants were of ‘double‐negative’ phenotype (le, se) and 19.3% were of single dominant non‐secretor phenotype (Le, se). Serum Lewis antigen CA19‐9 levels were significantly different between subgroups and consistent with the defined phenotype. Our study revealed the unique distribution of Lewis and Secretor polymorphisms in a large Chinese population, and decoded the combined genotypes of the two CA19‐9‐related genes. John Wiley and Sons Inc. 2017-10-04 /pmc/articles/PMC5666394/ /pubmed/29123975 http://dx.doi.org/10.1002/2211-5463.12278 Text en © 2017 The Authors. Published by FEBS Press and John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Guo, Meng
Luo, Guopei
Lu, Renquan
Shi, Weizhong
Cheng, He
Lu, Yu
Jin, Kaizhou
Yang, Chao
Wang, Zhengshi
Long, Jiang
Xu, Jin
Ni, Quanxing
Liu, Chen
Yu, Xianjun
Distribution of Lewis and Secretor polymorphisms and corresponding CA19‐9 antigen expression in a Chinese population
title Distribution of Lewis and Secretor polymorphisms and corresponding CA19‐9 antigen expression in a Chinese population
title_full Distribution of Lewis and Secretor polymorphisms and corresponding CA19‐9 antigen expression in a Chinese population
title_fullStr Distribution of Lewis and Secretor polymorphisms and corresponding CA19‐9 antigen expression in a Chinese population
title_full_unstemmed Distribution of Lewis and Secretor polymorphisms and corresponding CA19‐9 antigen expression in a Chinese population
title_short Distribution of Lewis and Secretor polymorphisms and corresponding CA19‐9 antigen expression in a Chinese population
title_sort distribution of lewis and secretor polymorphisms and corresponding ca19‐9 antigen expression in a chinese population
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5666394/
https://www.ncbi.nlm.nih.gov/pubmed/29123975
http://dx.doi.org/10.1002/2211-5463.12278
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