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Downregulated miRNA-1269a variant (rs73239138) decreases the susceptibility to gastric cancer via targeting ZNF70

Although emerging evidence has indicated that single nucleotide polymorphisms (SNPs) in microRNAs (miRNAs) are associated with susceptibility to gastric cancer, a limited number of studies have revealed the underlying molecular mechanisms. In the present study, the results suggested that miR-1269a r...

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Autores principales: Li, Wenshuai, Zhang, Huilu, Min, Pei, Zhu, Jie, Xu, Diannan, Jiang, Weiru, Ma, Yanyun, Qiu, Jigang, Xu, Weihong, Chen, Jian, Zhang, Mingqing, Li, Min, Yang, Dongqin, Shi, Jianping, Zhang, Jun, Liu, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5754851/
https://www.ncbi.nlm.nih.gov/pubmed/29344113
http://dx.doi.org/10.3892/ol.2017.7091
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author Li, Wenshuai
Zhang, Huilu
Min, Pei
Zhu, Jie
Xu, Diannan
Jiang, Weiru
Ma, Yanyun
Qiu, Jigang
Xu, Weihong
Chen, Jian
Zhang, Mingqing
Li, Min
Yang, Dongqin
Shi, Jianping
Zhang, Jun
Liu, Jie
author_facet Li, Wenshuai
Zhang, Huilu
Min, Pei
Zhu, Jie
Xu, Diannan
Jiang, Weiru
Ma, Yanyun
Qiu, Jigang
Xu, Weihong
Chen, Jian
Zhang, Mingqing
Li, Min
Yang, Dongqin
Shi, Jianping
Zhang, Jun
Liu, Jie
author_sort Li, Wenshuai
collection PubMed
description Although emerging evidence has indicated that single nucleotide polymorphisms (SNPs) in microRNAs (miRNAs) are associated with susceptibility to gastric cancer, a limited number of studies have revealed the underlying molecular mechanisms. In the present study, the results suggested that miR-1269a rs73239138 has a role in decreasing the risk of gastric cancer. The level of miR-1269a variant expression was significantly downregulated compared with the wild-type miR-1269a in the gastric cells (Fig. 1). Furthermore, overexpression of miR-1269a inhibited apoptosis of gastric cancer cells. Expression of the miR-1269a variant inhibited the function of miR-1269a by increasing the apoptotic rate and the expression of Bik, Bim and Bak was upregulated consistently. In addition, zinc-finger protein 70 (ZNF70) was identified to be a target gene of miR-1269a, which was downregulated by miR-1269a and upregulated by miR-1269a variant. ZNF70 was indicated to exert a role as a tumor suppressor in gastric cancer. To the best our knowledge, the present study for the first time highlights a critical role of miR-1269a variant rs73239138 in decreasing the susceptibility to gastric cancer by downregulating its expression and targeting ZNF70, which promotes apoptosis of gastric cancer cells. This SNP is indicated to serve as a potential biomarker and therapeutic target for gastric cancer.
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spelling pubmed-57548512018-01-17 Downregulated miRNA-1269a variant (rs73239138) decreases the susceptibility to gastric cancer via targeting ZNF70 Li, Wenshuai Zhang, Huilu Min, Pei Zhu, Jie Xu, Diannan Jiang, Weiru Ma, Yanyun Qiu, Jigang Xu, Weihong Chen, Jian Zhang, Mingqing Li, Min Yang, Dongqin Shi, Jianping Zhang, Jun Liu, Jie Oncol Lett Articles Although emerging evidence has indicated that single nucleotide polymorphisms (SNPs) in microRNAs (miRNAs) are associated with susceptibility to gastric cancer, a limited number of studies have revealed the underlying molecular mechanisms. In the present study, the results suggested that miR-1269a rs73239138 has a role in decreasing the risk of gastric cancer. The level of miR-1269a variant expression was significantly downregulated compared with the wild-type miR-1269a in the gastric cells (Fig. 1). Furthermore, overexpression of miR-1269a inhibited apoptosis of gastric cancer cells. Expression of the miR-1269a variant inhibited the function of miR-1269a by increasing the apoptotic rate and the expression of Bik, Bim and Bak was upregulated consistently. In addition, zinc-finger protein 70 (ZNF70) was identified to be a target gene of miR-1269a, which was downregulated by miR-1269a and upregulated by miR-1269a variant. ZNF70 was indicated to exert a role as a tumor suppressor in gastric cancer. To the best our knowledge, the present study for the first time highlights a critical role of miR-1269a variant rs73239138 in decreasing the susceptibility to gastric cancer by downregulating its expression and targeting ZNF70, which promotes apoptosis of gastric cancer cells. This SNP is indicated to serve as a potential biomarker and therapeutic target for gastric cancer. D.A. Spandidos 2017-12 2017-09-28 /pmc/articles/PMC5754851/ /pubmed/29344113 http://dx.doi.org/10.3892/ol.2017.7091 Text en Copyright: © Li et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Li, Wenshuai
Zhang, Huilu
Min, Pei
Zhu, Jie
Xu, Diannan
Jiang, Weiru
Ma, Yanyun
Qiu, Jigang
Xu, Weihong
Chen, Jian
Zhang, Mingqing
Li, Min
Yang, Dongqin
Shi, Jianping
Zhang, Jun
Liu, Jie
Downregulated miRNA-1269a variant (rs73239138) decreases the susceptibility to gastric cancer via targeting ZNF70
title Downregulated miRNA-1269a variant (rs73239138) decreases the susceptibility to gastric cancer via targeting ZNF70
title_full Downregulated miRNA-1269a variant (rs73239138) decreases the susceptibility to gastric cancer via targeting ZNF70
title_fullStr Downregulated miRNA-1269a variant (rs73239138) decreases the susceptibility to gastric cancer via targeting ZNF70
title_full_unstemmed Downregulated miRNA-1269a variant (rs73239138) decreases the susceptibility to gastric cancer via targeting ZNF70
title_short Downregulated miRNA-1269a variant (rs73239138) decreases the susceptibility to gastric cancer via targeting ZNF70
title_sort downregulated mirna-1269a variant (rs73239138) decreases the susceptibility to gastric cancer via targeting znf70
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5754851/
https://www.ncbi.nlm.nih.gov/pubmed/29344113
http://dx.doi.org/10.3892/ol.2017.7091
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