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miR-140-5p suppresses the proliferation, migration and invasion of gastric cancer by regulating YES1

BACKGROUND: The aberrant expression of microRNA-140-5p (miR-140-5p) has been described in gastric cancer (GC). However, the role of miR-140-5p in GC remains unclear. In this study, the prognostic relevance of miR-140-5p in GC was investigated and YES1 was identified as a novel target of miR-140-5p i...

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Autores principales: Fang, Zheng, Yin, Shuai, Sun, Ruochuan, Zhang, Shangxin, Fu, Min, Wu, Youliang, Zhang, Tao, Khaliq, Junaid, Li, Yongxiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5561618/
https://www.ncbi.nlm.nih.gov/pubmed/28818100
http://dx.doi.org/10.1186/s12943-017-0708-6
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author Fang, Zheng
Yin, Shuai
Sun, Ruochuan
Zhang, Shangxin
Fu, Min
Wu, Youliang
Zhang, Tao
Khaliq, Junaid
Li, Yongxiang
author_facet Fang, Zheng
Yin, Shuai
Sun, Ruochuan
Zhang, Shangxin
Fu, Min
Wu, Youliang
Zhang, Tao
Khaliq, Junaid
Li, Yongxiang
author_sort Fang, Zheng
collection PubMed
description BACKGROUND: The aberrant expression of microRNA-140-5p (miR-140-5p) has been described in gastric cancer (GC). However, the role of miR-140-5p in GC remains unclear. In this study, the prognostic relevance of miR-140-5p in GC was investigated and YES1 was identified as a novel target of miR-140-5p in regulating tumor progression. METHODS: miR-140-5p level was determined in 20 paired frozen specimens through quantitative real-time PCR, and analyzed in tissue microarrays through in situ hybridization. The target of miR-140-5p was verified through a dual luciferase reporter assay, and the effects of miR-140-5p on phenotypic changes in GC cells were investigated in vitro and in vivo. RESULTS: Compared with that in adjacent normal tissues, miR-140-5p expression decreased in cancerous tissues. The downregulated miR-140-5p in 144 patients with GC was significantly correlated with the reduced overall survival of these patients. miR-140-5p could inhibit GC cell proliferation, migration and invasion by directly targeting 3′–untranlated region of YES1. miR-140-5p could also remarkably reduce the tumor size in GC xenograft mice. CONCLUSIONS: miR-140-5p serves as a potential prognostic factor in patients with GC, and miR-140-5p mediated YES1 inhibition is a novel mechanism behind the suppressive effects of miR-140-5p in GC. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12943-017-0708-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-55616182017-08-18 miR-140-5p suppresses the proliferation, migration and invasion of gastric cancer by regulating YES1 Fang, Zheng Yin, Shuai Sun, Ruochuan Zhang, Shangxin Fu, Min Wu, Youliang Zhang, Tao Khaliq, Junaid Li, Yongxiang Mol Cancer Research BACKGROUND: The aberrant expression of microRNA-140-5p (miR-140-5p) has been described in gastric cancer (GC). However, the role of miR-140-5p in GC remains unclear. In this study, the prognostic relevance of miR-140-5p in GC was investigated and YES1 was identified as a novel target of miR-140-5p in regulating tumor progression. METHODS: miR-140-5p level was determined in 20 paired frozen specimens through quantitative real-time PCR, and analyzed in tissue microarrays through in situ hybridization. The target of miR-140-5p was verified through a dual luciferase reporter assay, and the effects of miR-140-5p on phenotypic changes in GC cells were investigated in vitro and in vivo. RESULTS: Compared with that in adjacent normal tissues, miR-140-5p expression decreased in cancerous tissues. The downregulated miR-140-5p in 144 patients with GC was significantly correlated with the reduced overall survival of these patients. miR-140-5p could inhibit GC cell proliferation, migration and invasion by directly targeting 3′–untranlated region of YES1. miR-140-5p could also remarkably reduce the tumor size in GC xenograft mice. CONCLUSIONS: miR-140-5p serves as a potential prognostic factor in patients with GC, and miR-140-5p mediated YES1 inhibition is a novel mechanism behind the suppressive effects of miR-140-5p in GC. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12943-017-0708-6) contains supplementary material, which is available to authorized users. BioMed Central 2017-08-17 /pmc/articles/PMC5561618/ /pubmed/28818100 http://dx.doi.org/10.1186/s12943-017-0708-6 Text en © The Author(s). 2017 Open AccessThis 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
Fang, Zheng
Yin, Shuai
Sun, Ruochuan
Zhang, Shangxin
Fu, Min
Wu, Youliang
Zhang, Tao
Khaliq, Junaid
Li, Yongxiang
miR-140-5p suppresses the proliferation, migration and invasion of gastric cancer by regulating YES1
title miR-140-5p suppresses the proliferation, migration and invasion of gastric cancer by regulating YES1
title_full miR-140-5p suppresses the proliferation, migration and invasion of gastric cancer by regulating YES1
title_fullStr miR-140-5p suppresses the proliferation, migration and invasion of gastric cancer by regulating YES1
title_full_unstemmed miR-140-5p suppresses the proliferation, migration and invasion of gastric cancer by regulating YES1
title_short miR-140-5p suppresses the proliferation, migration and invasion of gastric cancer by regulating YES1
title_sort mir-140-5p suppresses the proliferation, migration and invasion of gastric cancer by regulating yes1
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5561618/
https://www.ncbi.nlm.nih.gov/pubmed/28818100
http://dx.doi.org/10.1186/s12943-017-0708-6
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