MiR-129-5p influences the progression of gastric cancer cells through interacting with

The purpose of our study is to clarify the effect of microRNA-129-5p in the progression of human gastric cancer cells by regulating SPOCK1 . The expression of microRNA-129-5p and SPOCK1 was tested by quantitative real-time polymerase chain reaction in tissues and cell lines. We validated the targete...

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Main Authors: Lei Yan, Kai Sun, Yang Liu, Jun Liang, Kerui Cai, Jinqiu Gui
Format: Article
Language:English
Published: SAGE Publishing 2017-06-01
Series:Tumor Biology
Online Access:https://doi.org/10.1177/1010428317706916
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author Lei Yan
Kai Sun
Yang Liu
Jun Liang
Kerui Cai
Jinqiu Gui
author_facet Lei Yan
Kai Sun
Yang Liu
Jun Liang
Kerui Cai
Jinqiu Gui
author_sort Lei Yan
collection DOAJ
description The purpose of our study is to clarify the effect of microRNA-129-5p in the progression of human gastric cancer cells by regulating SPOCK1 . The expression of microRNA-129-5p and SPOCK1 was tested by quantitative real-time polymerase chain reaction in tissues and cell lines. We validated the targeted relationship between microRNA-129-5p and SPOCK1 by dual luciferase reporter gene assay. 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide, colony formation, flow cytometry, transwell, and wound scratch assays were used to analyze the effects of microRNA-129-5p on SGC-7901 cell viability, proliferation, cell cycle and apoptosis, invasiveness, and migration. MicroRNA-129-5p was downregulated while SPOCK1 was upregulated in gastric cancer tissues and cell lines. The result of luciferase reporter gene assay demonstrated that microRNA-129-5p can target SPOCK1 by binding to the 3′untranslated region. The overexpression of microRNA-129-5p or the inhibition of SPOCK1 inhibited SGC-7901 viability, proliferation, migration, and invasion while promoted cell cycle arrest in G0/G1 stage and cell apoptosis. Our results suggested that microRNA-129-5p could directly specifically suppress SPOCK1 , which might be one of the potential mechanisms in inhibiting cell processes including viability, proliferation, cell mitosis, migration, and invasiveness of gastric cancer cells.
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spelling doaj-art-fd7485ebbbe94484bc8fa97af7b552a02025-08-20T02:49:49ZengSAGE PublishingTumor Biology1423-03802017-06-013910.1177/1010428317706916MiR-129-5p influences the progression of gastric cancer cells through interacting withLei Yan0Kai Sun1Yang Liu2Jun Liang3Kerui Cai4Jinqiu Gui5Department of Histology and Embryology, Mudanjiang Medical University, Mudanjiang, People’s Republic of ChinaDepartment of Biology, Mudanjiang Medical University, Mudanjiang, People’s Republic of ChinaDepartment of Pathogenic Microbiology and Immunology, Mudanjiang Medical University, Mudanjiang, People’s Republic of ChinaDepartment of Histology and Embryology, Mudanjiang Medical University, Mudanjiang, People’s Republic of ChinaDepartment of Histology and Embryology, Mudanjiang Medical University, Mudanjiang, People’s Republic of ChinaDepartment of Pathogenic Microbiology and Immunology, Mudanjiang Medical University, Mudanjiang, People’s Republic of ChinaThe purpose of our study is to clarify the effect of microRNA-129-5p in the progression of human gastric cancer cells by regulating SPOCK1 . The expression of microRNA-129-5p and SPOCK1 was tested by quantitative real-time polymerase chain reaction in tissues and cell lines. We validated the targeted relationship between microRNA-129-5p and SPOCK1 by dual luciferase reporter gene assay. 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide, colony formation, flow cytometry, transwell, and wound scratch assays were used to analyze the effects of microRNA-129-5p on SGC-7901 cell viability, proliferation, cell cycle and apoptosis, invasiveness, and migration. MicroRNA-129-5p was downregulated while SPOCK1 was upregulated in gastric cancer tissues and cell lines. The result of luciferase reporter gene assay demonstrated that microRNA-129-5p can target SPOCK1 by binding to the 3′untranslated region. The overexpression of microRNA-129-5p or the inhibition of SPOCK1 inhibited SGC-7901 viability, proliferation, migration, and invasion while promoted cell cycle arrest in G0/G1 stage and cell apoptosis. Our results suggested that microRNA-129-5p could directly specifically suppress SPOCK1 , which might be one of the potential mechanisms in inhibiting cell processes including viability, proliferation, cell mitosis, migration, and invasiveness of gastric cancer cells.https://doi.org/10.1177/1010428317706916
spellingShingle Lei Yan
Kai Sun
Yang Liu
Jun Liang
Kerui Cai
Jinqiu Gui
MiR-129-5p influences the progression of gastric cancer cells through interacting with
Tumor Biology
title MiR-129-5p influences the progression of gastric cancer cells through interacting with
title_full MiR-129-5p influences the progression of gastric cancer cells through interacting with
title_fullStr MiR-129-5p influences the progression of gastric cancer cells through interacting with
title_full_unstemmed MiR-129-5p influences the progression of gastric cancer cells through interacting with
title_short MiR-129-5p influences the progression of gastric cancer cells through interacting with
title_sort mir 129 5p influences the progression of gastric cancer cells through interacting with
url https://doi.org/10.1177/1010428317706916
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