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A functional variant rs353292 in the flanking region of miR-143/145 contributes to the risk of colorectal cancer

MicroRNA (miR)-143 and miR-145 have been identified as molecular regulators in cell proliferation, cell growth, clone formation, apoptosis, cell cycle, invasion, and migration. We previously found that rs353292 in the flanking region of miR-143/145 showed a high frequency in patients with colorectal...

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Autores principales: Yuan, Fang, Sun, Ruifen, Li, Lijuan, Jin, Bo, Wang, Yanyun, Liang, Yundan, Che, Guanglu, Gao, Linbo, Zhang, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4957080/
https://www.ncbi.nlm.nih.gov/pubmed/27444415
http://dx.doi.org/10.1038/srep30195
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author Yuan, Fang
Sun, Ruifen
Li, Lijuan
Jin, Bo
Wang, Yanyun
Liang, Yundan
Che, Guanglu
Gao, Linbo
Zhang, Lin
author_facet Yuan, Fang
Sun, Ruifen
Li, Lijuan
Jin, Bo
Wang, Yanyun
Liang, Yundan
Che, Guanglu
Gao, Linbo
Zhang, Lin
author_sort Yuan, Fang
collection PubMed
description MicroRNA (miR)-143 and miR-145 have been identified as molecular regulators in cell proliferation, cell growth, clone formation, apoptosis, cell cycle, invasion, and migration. We previously found that rs353292 in the flanking region of miR-143/145 showed a high frequency in patients with colorectal cancer (CRC). To identify whether the rs353292 polymorphism is a risk factor for CRC, we conducted this study with larger samples. A total of 809 patients with CRC and 1005 gender matched controls were collected. The rs353292 polymorphism was genotyped by using TaqMan allelic discrimination. Dual luciferase reporter assay was carried out to measure the transcriptional activity. We found that the rs353292 polymorphism was associated with an increased risk for developing CRC in heterozygous comparison (adjusted OR = 1.70, 95% CI, 1.32–2.20, P < 0.001), dominant genetic model (adjusted OR = 1.62, 95% CI, 1.26–2.09, P < 0.001), and allele comparison (adjusted OR = 1.46, 95% CI, 1.16–1.84, P = 0.001). The rs353292 CT/TT carriers exhibited a lower expression of miR-143 compared to the CC carriers (P = 0.04). Moreover, the pGL3-rs353292T displayed a significantly lower luciferase activity than pGL3-rs353292C (P < 0.01). These findings indicate that the rs353292 polymorphism is functional and may be a risk factor for the development of CRC.
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spelling pubmed-49570802016-07-26 A functional variant rs353292 in the flanking region of miR-143/145 contributes to the risk of colorectal cancer Yuan, Fang Sun, Ruifen Li, Lijuan Jin, Bo Wang, Yanyun Liang, Yundan Che, Guanglu Gao, Linbo Zhang, Lin Sci Rep Article MicroRNA (miR)-143 and miR-145 have been identified as molecular regulators in cell proliferation, cell growth, clone formation, apoptosis, cell cycle, invasion, and migration. We previously found that rs353292 in the flanking region of miR-143/145 showed a high frequency in patients with colorectal cancer (CRC). To identify whether the rs353292 polymorphism is a risk factor for CRC, we conducted this study with larger samples. A total of 809 patients with CRC and 1005 gender matched controls were collected. The rs353292 polymorphism was genotyped by using TaqMan allelic discrimination. Dual luciferase reporter assay was carried out to measure the transcriptional activity. We found that the rs353292 polymorphism was associated with an increased risk for developing CRC in heterozygous comparison (adjusted OR = 1.70, 95% CI, 1.32–2.20, P < 0.001), dominant genetic model (adjusted OR = 1.62, 95% CI, 1.26–2.09, P < 0.001), and allele comparison (adjusted OR = 1.46, 95% CI, 1.16–1.84, P = 0.001). The rs353292 CT/TT carriers exhibited a lower expression of miR-143 compared to the CC carriers (P = 0.04). Moreover, the pGL3-rs353292T displayed a significantly lower luciferase activity than pGL3-rs353292C (P < 0.01). These findings indicate that the rs353292 polymorphism is functional and may be a risk factor for the development of CRC. Nature Publishing Group 2016-07-22 /pmc/articles/PMC4957080/ /pubmed/27444415 http://dx.doi.org/10.1038/srep30195 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Yuan, Fang
Sun, Ruifen
Li, Lijuan
Jin, Bo
Wang, Yanyun
Liang, Yundan
Che, Guanglu
Gao, Linbo
Zhang, Lin
A functional variant rs353292 in the flanking region of miR-143/145 contributes to the risk of colorectal cancer
title A functional variant rs353292 in the flanking region of miR-143/145 contributes to the risk of colorectal cancer
title_full A functional variant rs353292 in the flanking region of miR-143/145 contributes to the risk of colorectal cancer
title_fullStr A functional variant rs353292 in the flanking region of miR-143/145 contributes to the risk of colorectal cancer
title_full_unstemmed A functional variant rs353292 in the flanking region of miR-143/145 contributes to the risk of colorectal cancer
title_short A functional variant rs353292 in the flanking region of miR-143/145 contributes to the risk of colorectal cancer
title_sort functional variant rs353292 in the flanking region of mir-143/145 contributes to the risk of colorectal cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4957080/
https://www.ncbi.nlm.nih.gov/pubmed/27444415
http://dx.doi.org/10.1038/srep30195
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