Cargando…
Vasodilator-stimulated phosphoprotein (VASP), a novel target of miR-4455, promotes gastric cancer cell proliferation, migration, and invasion, through activating the PI3K/AKT signaling pathway
BACKGROUND: MicroRNAs (miRNAs) are small non-coding RNAs which play important roles in the carcinogenesis of gastric cancer (GC). Expression profiling of miRNAs in paired gastric cancer and adjacent normal gastric tissues has demonstrated that miR-4455 is down-regulated in gastric cancer tissues, bu...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6038240/ https://www.ncbi.nlm.nih.gov/pubmed/30002604 http://dx.doi.org/10.1186/s12935-018-0573-4 |
_version_ | 1783338457921224704 |
---|---|
author | Chen, Haiqun Dai, Gang Cai, Yiting Gong, Qinhao Wu, Wei Gao, Min Fei, Zhewei |
author_facet | Chen, Haiqun Dai, Gang Cai, Yiting Gong, Qinhao Wu, Wei Gao, Min Fei, Zhewei |
author_sort | Chen, Haiqun |
collection | PubMed |
description | BACKGROUND: MicroRNAs (miRNAs) are small non-coding RNAs which play important roles in the carcinogenesis of gastric cancer (GC). Expression profiling of miRNAs in paired gastric cancer and adjacent normal gastric tissues has demonstrated that miR-4455 is down-regulated in gastric cancer tissues, but its functional role in the carcinogenesis of GC had not previously been investigated. AIMS: The purpose of this study was to investigate the functional and biological mechanisms of miR-4455 in the progression of GC, in vitro. METHODS: Expression of miR-4455 was compared in human GC tissue samples and paired adjacent normal tissue samples. The in vitro effects of miR-4455 expression in MGC-803 cells on their proliferation, invasion, and migration were assessed by MTT assays and 5-bromo-2′-deoxyuridine staining, matrigel-invasion analysis and wound healing assays. Bioinformatics analysis (using PicTar, target scan and miRBase target) was used to identify potential targets for miR-4455, and the luciferase reporter assay, qRT-PCR and Western-blotting analyses were used to confirm VASP as the target of miR-4455. In addition, the effects of downregulation of VASP on the activation of PI3K/AKT signaling pathway were measured using Western-blot analysis. RESULTS: The expression of miR-4455 was markedly down-regulated in gastric cancer tissues vs. adjacent normal tissues, and miR-4455 expression inhibited the proliferation, invasion and migration of MGC-803 GC cells in vitro. Luciferase reporter assays revealed that miR-4455 inhibited VASP expression by targeting the 3′-UTR sequence of VASP. Furthermore, silencing of VASP markedly inhibited the activation of the PI3K/AKT signaling pathway. CONCLUSION: Our results suggest that miR-4455 functions as a tumor suppressor in gastric cancer, by targeting VASP leading to activation of the PI3K/AKT signaling pathway and the inhibition of VASP mediated proliferation, migration and invasion of gastric cancer cells. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12935-018-0573-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6038240 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-60382402018-07-12 Vasodilator-stimulated phosphoprotein (VASP), a novel target of miR-4455, promotes gastric cancer cell proliferation, migration, and invasion, through activating the PI3K/AKT signaling pathway Chen, Haiqun Dai, Gang Cai, Yiting Gong, Qinhao Wu, Wei Gao, Min Fei, Zhewei Cancer Cell Int Primary Research BACKGROUND: MicroRNAs (miRNAs) are small non-coding RNAs which play important roles in the carcinogenesis of gastric cancer (GC). Expression profiling of miRNAs in paired gastric cancer and adjacent normal gastric tissues has demonstrated that miR-4455 is down-regulated in gastric cancer tissues, but its functional role in the carcinogenesis of GC had not previously been investigated. AIMS: The purpose of this study was to investigate the functional and biological mechanisms of miR-4455 in the progression of GC, in vitro. METHODS: Expression of miR-4455 was compared in human GC tissue samples and paired adjacent normal tissue samples. The in vitro effects of miR-4455 expression in MGC-803 cells on their proliferation, invasion, and migration were assessed by MTT assays and 5-bromo-2′-deoxyuridine staining, matrigel-invasion analysis and wound healing assays. Bioinformatics analysis (using PicTar, target scan and miRBase target) was used to identify potential targets for miR-4455, and the luciferase reporter assay, qRT-PCR and Western-blotting analyses were used to confirm VASP as the target of miR-4455. In addition, the effects of downregulation of VASP on the activation of PI3K/AKT signaling pathway were measured using Western-blot analysis. RESULTS: The expression of miR-4455 was markedly down-regulated in gastric cancer tissues vs. adjacent normal tissues, and miR-4455 expression inhibited the proliferation, invasion and migration of MGC-803 GC cells in vitro. Luciferase reporter assays revealed that miR-4455 inhibited VASP expression by targeting the 3′-UTR sequence of VASP. Furthermore, silencing of VASP markedly inhibited the activation of the PI3K/AKT signaling pathway. CONCLUSION: Our results suggest that miR-4455 functions as a tumor suppressor in gastric cancer, by targeting VASP leading to activation of the PI3K/AKT signaling pathway and the inhibition of VASP mediated proliferation, migration and invasion of gastric cancer cells. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12935-018-0573-4) contains supplementary material, which is available to authorized users. BioMed Central 2018-07-09 /pmc/articles/PMC6038240/ /pubmed/30002604 http://dx.doi.org/10.1186/s12935-018-0573-4 Text en © The Author(s) 2018 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 | Primary Research Chen, Haiqun Dai, Gang Cai, Yiting Gong, Qinhao Wu, Wei Gao, Min Fei, Zhewei Vasodilator-stimulated phosphoprotein (VASP), a novel target of miR-4455, promotes gastric cancer cell proliferation, migration, and invasion, through activating the PI3K/AKT signaling pathway |
title | Vasodilator-stimulated phosphoprotein (VASP), a novel target of miR-4455, promotes gastric cancer cell proliferation, migration, and invasion, through activating the PI3K/AKT signaling pathway |
title_full | Vasodilator-stimulated phosphoprotein (VASP), a novel target of miR-4455, promotes gastric cancer cell proliferation, migration, and invasion, through activating the PI3K/AKT signaling pathway |
title_fullStr | Vasodilator-stimulated phosphoprotein (VASP), a novel target of miR-4455, promotes gastric cancer cell proliferation, migration, and invasion, through activating the PI3K/AKT signaling pathway |
title_full_unstemmed | Vasodilator-stimulated phosphoprotein (VASP), a novel target of miR-4455, promotes gastric cancer cell proliferation, migration, and invasion, through activating the PI3K/AKT signaling pathway |
title_short | Vasodilator-stimulated phosphoprotein (VASP), a novel target of miR-4455, promotes gastric cancer cell proliferation, migration, and invasion, through activating the PI3K/AKT signaling pathway |
title_sort | vasodilator-stimulated phosphoprotein (vasp), a novel target of mir-4455, promotes gastric cancer cell proliferation, migration, and invasion, through activating the pi3k/akt signaling pathway |
topic | Primary Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6038240/ https://www.ncbi.nlm.nih.gov/pubmed/30002604 http://dx.doi.org/10.1186/s12935-018-0573-4 |
work_keys_str_mv | AT chenhaiqun vasodilatorstimulatedphosphoproteinvaspanoveltargetofmir4455promotesgastriccancercellproliferationmigrationandinvasionthroughactivatingthepi3kaktsignalingpathway AT daigang vasodilatorstimulatedphosphoproteinvaspanoveltargetofmir4455promotesgastriccancercellproliferationmigrationandinvasionthroughactivatingthepi3kaktsignalingpathway AT caiyiting vasodilatorstimulatedphosphoproteinvaspanoveltargetofmir4455promotesgastriccancercellproliferationmigrationandinvasionthroughactivatingthepi3kaktsignalingpathway AT gongqinhao vasodilatorstimulatedphosphoproteinvaspanoveltargetofmir4455promotesgastriccancercellproliferationmigrationandinvasionthroughactivatingthepi3kaktsignalingpathway AT wuwei vasodilatorstimulatedphosphoproteinvaspanoveltargetofmir4455promotesgastriccancercellproliferationmigrationandinvasionthroughactivatingthepi3kaktsignalingpathway AT gaomin vasodilatorstimulatedphosphoproteinvaspanoveltargetofmir4455promotesgastriccancercellproliferationmigrationandinvasionthroughactivatingthepi3kaktsignalingpathway AT feizhewei vasodilatorstimulatedphosphoproteinvaspanoveltargetofmir4455promotesgastriccancercellproliferationmigrationandinvasionthroughactivatingthepi3kaktsignalingpathway |