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Genetic variations of MUC17 are associated with endometriosis development and related infertility

BACKGROUND: Genetic alterations of mucin genes, such as MUC2 and MUC4, were previously identified to be associated with endometriosis and related infertility. Additionally, gene expression profiling has confirmed MUC17 to be overexpressed in mucinous ovarian carcinoma; however, its associated risk f...

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Autores principales: Yang, Ching-Wen, Chang, Cherry Yin-Yi, Lai, Ming-Tsung, Chang, Hui-Wen, Lu, Cheng-Chan, Chen, Yi, Chen, Chih-Mei, Lee, Shan-Chih, Tsai, Pei-Wen, Yang, Su-Han, Lin, Chih-Hung, Sheu, Jim Jinn-Chyuan, Tsai, Fuu-Jen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4593232/
https://www.ncbi.nlm.nih.gov/pubmed/26285705
http://dx.doi.org/10.1186/s12881-015-0209-7
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author Yang, Ching-Wen
Chang, Cherry Yin-Yi
Lai, Ming-Tsung
Chang, Hui-Wen
Lu, Cheng-Chan
Chen, Yi
Chen, Chih-Mei
Lee, Shan-Chih
Tsai, Pei-Wen
Yang, Su-Han
Lin, Chih-Hung
Sheu, Jim Jinn-Chyuan
Tsai, Fuu-Jen
author_facet Yang, Ching-Wen
Chang, Cherry Yin-Yi
Lai, Ming-Tsung
Chang, Hui-Wen
Lu, Cheng-Chan
Chen, Yi
Chen, Chih-Mei
Lee, Shan-Chih
Tsai, Pei-Wen
Yang, Su-Han
Lin, Chih-Hung
Sheu, Jim Jinn-Chyuan
Tsai, Fuu-Jen
author_sort Yang, Ching-Wen
collection PubMed
description BACKGROUND: Genetic alterations of mucin genes, such as MUC2 and MUC4, were previously identified to be associated with endometriosis and related infertility. Additionally, gene expression profiling has confirmed MUC17 to be overexpressed in mucinous ovarian carcinoma; however, its associated risk for endometriosis remains unclear. This study was focused on the potential impact of genetic variations in MUC17 on endometriosis development and associated clinical features. METHODS: The study subjects included 189 female Taiwanese patients with pathology-proven endometriosis and 191 healthy Taiwanese women as controls. Five single-nucleotide polymorphisms (rs4729645, rs10953316, rs74974199, rs4729655, and rs4729656) within the MUC17 gene were selected and genotyped using the Taqman genotyping assay to examine the allele frequency and genotype distributions of MUC17 polymorphisms. RESULTS: Genotyping revealed that the A allele at rs10953316 in MUC17 was a protective genetic factor in endometriosis development (p = 0.008; OR = 0.53; 95 % CI: 0.36-0.79). Genetic variation of rs4729655 protected patients against endometriosis-induced infertility, but was associated with a higher cancer antigen 125 (CA125) level. Base-pairing analysis, called MaxExpect, predicted an additional loop in the mRNA structure caused by rs10953316 polymorphism, possibly influencing ribosome sliding and translation efficiency. Such predictions were confirmed by immunohistochemistry that patients with AA genotype at rs10953316 showed low MUC17 levels in their endometrium, patients with GA genotype showed moderate levels, and strong staining could be found in patients with GG genotype. CONCLUSIONS: MUC17 polymorphisms are involved in endometriosis development and the associated infertility in the Taiwanese population. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12881-015-0209-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-45932322015-10-06 Genetic variations of MUC17 are associated with endometriosis development and related infertility Yang, Ching-Wen Chang, Cherry Yin-Yi Lai, Ming-Tsung Chang, Hui-Wen Lu, Cheng-Chan Chen, Yi Chen, Chih-Mei Lee, Shan-Chih Tsai, Pei-Wen Yang, Su-Han Lin, Chih-Hung Sheu, Jim Jinn-Chyuan Tsai, Fuu-Jen BMC Med Genet Research Article BACKGROUND: Genetic alterations of mucin genes, such as MUC2 and MUC4, were previously identified to be associated with endometriosis and related infertility. Additionally, gene expression profiling has confirmed MUC17 to be overexpressed in mucinous ovarian carcinoma; however, its associated risk for endometriosis remains unclear. This study was focused on the potential impact of genetic variations in MUC17 on endometriosis development and associated clinical features. METHODS: The study subjects included 189 female Taiwanese patients with pathology-proven endometriosis and 191 healthy Taiwanese women as controls. Five single-nucleotide polymorphisms (rs4729645, rs10953316, rs74974199, rs4729655, and rs4729656) within the MUC17 gene were selected and genotyped using the Taqman genotyping assay to examine the allele frequency and genotype distributions of MUC17 polymorphisms. RESULTS: Genotyping revealed that the A allele at rs10953316 in MUC17 was a protective genetic factor in endometriosis development (p = 0.008; OR = 0.53; 95 % CI: 0.36-0.79). Genetic variation of rs4729655 protected patients against endometriosis-induced infertility, but was associated with a higher cancer antigen 125 (CA125) level. Base-pairing analysis, called MaxExpect, predicted an additional loop in the mRNA structure caused by rs10953316 polymorphism, possibly influencing ribosome sliding and translation efficiency. Such predictions were confirmed by immunohistochemistry that patients with AA genotype at rs10953316 showed low MUC17 levels in their endometrium, patients with GA genotype showed moderate levels, and strong staining could be found in patients with GG genotype. CONCLUSIONS: MUC17 polymorphisms are involved in endometriosis development and the associated infertility in the Taiwanese population. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12881-015-0209-7) contains supplementary material, which is available to authorized users. BioMed Central 2015-08-19 /pmc/articles/PMC4593232/ /pubmed/26285705 http://dx.doi.org/10.1186/s12881-015-0209-7 Text en © Yang et al. 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Yang, Ching-Wen
Chang, Cherry Yin-Yi
Lai, Ming-Tsung
Chang, Hui-Wen
Lu, Cheng-Chan
Chen, Yi
Chen, Chih-Mei
Lee, Shan-Chih
Tsai, Pei-Wen
Yang, Su-Han
Lin, Chih-Hung
Sheu, Jim Jinn-Chyuan
Tsai, Fuu-Jen
Genetic variations of MUC17 are associated with endometriosis development and related infertility
title Genetic variations of MUC17 are associated with endometriosis development and related infertility
title_full Genetic variations of MUC17 are associated with endometriosis development and related infertility
title_fullStr Genetic variations of MUC17 are associated with endometriosis development and related infertility
title_full_unstemmed Genetic variations of MUC17 are associated with endometriosis development and related infertility
title_short Genetic variations of MUC17 are associated with endometriosis development and related infertility
title_sort genetic variations of muc17 are associated with endometriosis development and related infertility
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4593232/
https://www.ncbi.nlm.nih.gov/pubmed/26285705
http://dx.doi.org/10.1186/s12881-015-0209-7
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