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Reduced alternative splicing of estrogen receptor alpha in the endometrium of women with endometriosis
Endometriosis is a condition which involves the presence of uterine stroma and glands outside of the uterine cavity and represents one of the most prevalent disorders of the female reproductive tract. The key symptom of endometriosis is pain, including dysmenorrhea, deep dyspareunia, and chronic pel...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5746374/ https://www.ncbi.nlm.nih.gov/pubmed/29299139 http://dx.doi.org/10.18632/oncotarget.22701 |
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author | Zhang, Ying Zhang, Yong Zhao, Chunbo Yu, Tiantian Liu, Ye Shi, Weihui Shi, Fengtao Liu, Xinmei Sheng, Jianzhong Huang, Hefeng Xu, Hong |
author_facet | Zhang, Ying Zhang, Yong Zhao, Chunbo Yu, Tiantian Liu, Ye Shi, Weihui Shi, Fengtao Liu, Xinmei Sheng, Jianzhong Huang, Hefeng Xu, Hong |
author_sort | Zhang, Ying |
collection | PubMed |
description | Endometriosis is a condition which involves the presence of uterine stroma and glands outside of the uterine cavity and represents one of the most prevalent disorders of the female reproductive tract. The key symptom of endometriosis is pain, including dysmenorrhea, deep dyspareunia, and chronic pelvic pain. As such, endometriosis has significant economic consequences within the healthcare system and can influence the daily quality of life in affected patients. However, the pathophysiology of this disease and the mechanisms in which this condition generates pain are very unclear. This study, involving 30 women with endometriosis and 28 controls without endometriosis, aimed to investigate relative levels of estrogen receptor alpha (ERα) splice variants in the endometrium of women with and without endometriosis and investigate potential links to the severity of pain. Wild type (wt)-ERα was dominantly expressed in human endometrium while the expression of ERα-del.4, ERα-del.7, and ERα-del.3,4 was significantly reduced in endometriosis patients compared with healthy patients (p < 0.05). Furthermore, the relative ratios of wtERα:ERα-del.4, and wtERα:ERα-del.3,4 were associated with the severity of pain in endometriosis patients (p < 0.05). Consequently, analyzing differences in the relative levels of four types of ERα splice variant in the endometrium of patients with endometriosis may help in the development of endometriosis-targeted treatment and the development of appropriate therapies. |
format | Online Article Text |
id | pubmed-5746374 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-57463742018-01-03 Reduced alternative splicing of estrogen receptor alpha in the endometrium of women with endometriosis Zhang, Ying Zhang, Yong Zhao, Chunbo Yu, Tiantian Liu, Ye Shi, Weihui Shi, Fengtao Liu, Xinmei Sheng, Jianzhong Huang, Hefeng Xu, Hong Oncotarget Research Paper Endometriosis is a condition which involves the presence of uterine stroma and glands outside of the uterine cavity and represents one of the most prevalent disorders of the female reproductive tract. The key symptom of endometriosis is pain, including dysmenorrhea, deep dyspareunia, and chronic pelvic pain. As such, endometriosis has significant economic consequences within the healthcare system and can influence the daily quality of life in affected patients. However, the pathophysiology of this disease and the mechanisms in which this condition generates pain are very unclear. This study, involving 30 women with endometriosis and 28 controls without endometriosis, aimed to investigate relative levels of estrogen receptor alpha (ERα) splice variants in the endometrium of women with and without endometriosis and investigate potential links to the severity of pain. Wild type (wt)-ERα was dominantly expressed in human endometrium while the expression of ERα-del.4, ERα-del.7, and ERα-del.3,4 was significantly reduced in endometriosis patients compared with healthy patients (p < 0.05). Furthermore, the relative ratios of wtERα:ERα-del.4, and wtERα:ERα-del.3,4 were associated with the severity of pain in endometriosis patients (p < 0.05). Consequently, analyzing differences in the relative levels of four types of ERα splice variant in the endometrium of patients with endometriosis may help in the development of endometriosis-targeted treatment and the development of appropriate therapies. Impact Journals LLC 2017-11-27 /pmc/articles/PMC5746374/ /pubmed/29299139 http://dx.doi.org/10.18632/oncotarget.22701 Text en Copyright: © 2017 Zhang et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Research Paper Zhang, Ying Zhang, Yong Zhao, Chunbo Yu, Tiantian Liu, Ye Shi, Weihui Shi, Fengtao Liu, Xinmei Sheng, Jianzhong Huang, Hefeng Xu, Hong Reduced alternative splicing of estrogen receptor alpha in the endometrium of women with endometriosis |
title | Reduced alternative splicing of estrogen receptor alpha in the endometrium of women with endometriosis |
title_full | Reduced alternative splicing of estrogen receptor alpha in the endometrium of women with endometriosis |
title_fullStr | Reduced alternative splicing of estrogen receptor alpha in the endometrium of women with endometriosis |
title_full_unstemmed | Reduced alternative splicing of estrogen receptor alpha in the endometrium of women with endometriosis |
title_short | Reduced alternative splicing of estrogen receptor alpha in the endometrium of women with endometriosis |
title_sort | reduced alternative splicing of estrogen receptor alpha in the endometrium of women with endometriosis |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5746374/ https://www.ncbi.nlm.nih.gov/pubmed/29299139 http://dx.doi.org/10.18632/oncotarget.22701 |
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