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Circular RNA 0000096 affects cell growth and migration in gastric cancer
BACKGROUND: Circular RNAs (circRNAs) are a class of non-coding RNAs broadly expressed in cells of various species. Their role in cancers, especially in gastric cancer, is poorly understood. METHODS: Circular RNA 0000096 (hsa_circ_0000096) levels in 101 paired gastric cancer tissues and adjacent non-...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5344286/ https://www.ncbi.nlm.nih.gov/pubmed/28081541 http://dx.doi.org/10.1038/bjc.2016.451 |
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author | Li, Peifei Chen, Huilin Chen, Shengcan Mo, Xiaoyan Li, Tianwen Xiao, Bingxiu Yu, Rui Guo, Junming |
author_facet | Li, Peifei Chen, Huilin Chen, Shengcan Mo, Xiaoyan Li, Tianwen Xiao, Bingxiu Yu, Rui Guo, Junming |
author_sort | Li, Peifei |
collection | PubMed |
description | BACKGROUND: Circular RNAs (circRNAs) are a class of non-coding RNAs broadly expressed in cells of various species. Their role in cancers, especially in gastric cancer, is poorly understood. METHODS: Circular RNA 0000096 (hsa_circ_0000096) levels in 101 paired gastric cancer tissues and adjacent non-tumorous tissues from patients with gastric cancer were detected by real-time quantitative reverse transcription-polymerase chain reaction. A receiver operating characteristic curve was generated to evaluate the diagnostic value of hsa_circ_0000096. RNA interference was used to manipulate the expression of hsa_circ_0000096. Its biological effects were evaluated by flow cytometry, real-time cell analysis, a wound scratch assay, western blot analysis and xenograft models. RESULTS: Hsa_circ_0000096 was found to be significantly downregulated in gastric cancer tissues and gastric cancer cell lines compared with paired adjacent non-tumorous tissues and normal gastric epithelial cells (P<0.001). Moreover, knockdown of hsa_circ_0000096 significantly inhibited cell proliferation and migration in vitro and in vivo. The results of both immunohistochemical and western blot analyses showed that the protein levels of cyclin D1, cyclin-dependent kinase 6 (CDK6), matrix metalloproteinase-2 and MMP-9 were significantly reduced in vitro and in vivo. A gastric cancer xenograft nude mouse model indicated that Ki67 and VEGF were reduced in a dose-dependent manner following knockdown of hsa_circ_0000096. However, the expression of E-cadherin increased. CONCLUSIONS: Hsa_circ_0000096 may be used as a potential novel biomarker for gastric cancer. It affects gastric cancer cell growth and migration by regulating cyclin D1, CDK6, MMP-2 and MMP-9. |
format | Online Article Text |
id | pubmed-5344286 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53442862018-02-28 Circular RNA 0000096 affects cell growth and migration in gastric cancer Li, Peifei Chen, Huilin Chen, Shengcan Mo, Xiaoyan Li, Tianwen Xiao, Bingxiu Yu, Rui Guo, Junming Br J Cancer Molecular Diagnostics BACKGROUND: Circular RNAs (circRNAs) are a class of non-coding RNAs broadly expressed in cells of various species. Their role in cancers, especially in gastric cancer, is poorly understood. METHODS: Circular RNA 0000096 (hsa_circ_0000096) levels in 101 paired gastric cancer tissues and adjacent non-tumorous tissues from patients with gastric cancer were detected by real-time quantitative reverse transcription-polymerase chain reaction. A receiver operating characteristic curve was generated to evaluate the diagnostic value of hsa_circ_0000096. RNA interference was used to manipulate the expression of hsa_circ_0000096. Its biological effects were evaluated by flow cytometry, real-time cell analysis, a wound scratch assay, western blot analysis and xenograft models. RESULTS: Hsa_circ_0000096 was found to be significantly downregulated in gastric cancer tissues and gastric cancer cell lines compared with paired adjacent non-tumorous tissues and normal gastric epithelial cells (P<0.001). Moreover, knockdown of hsa_circ_0000096 significantly inhibited cell proliferation and migration in vitro and in vivo. The results of both immunohistochemical and western blot analyses showed that the protein levels of cyclin D1, cyclin-dependent kinase 6 (CDK6), matrix metalloproteinase-2 and MMP-9 were significantly reduced in vitro and in vivo. A gastric cancer xenograft nude mouse model indicated that Ki67 and VEGF were reduced in a dose-dependent manner following knockdown of hsa_circ_0000096. However, the expression of E-cadherin increased. CONCLUSIONS: Hsa_circ_0000096 may be used as a potential novel biomarker for gastric cancer. It affects gastric cancer cell growth and migration by regulating cyclin D1, CDK6, MMP-2 and MMP-9. Nature Publishing Group 2017-02-28 2017-01-12 /pmc/articles/PMC5344286/ /pubmed/28081541 http://dx.doi.org/10.1038/bjc.2016.451 Text en Copyright © 2017 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Molecular Diagnostics Li, Peifei Chen, Huilin Chen, Shengcan Mo, Xiaoyan Li, Tianwen Xiao, Bingxiu Yu, Rui Guo, Junming Circular RNA 0000096 affects cell growth and migration in gastric cancer |
title | Circular RNA 0000096 affects cell growth and migration in gastric cancer |
title_full | Circular RNA 0000096 affects cell growth and migration in gastric cancer |
title_fullStr | Circular RNA 0000096 affects cell growth and migration in gastric cancer |
title_full_unstemmed | Circular RNA 0000096 affects cell growth and migration in gastric cancer |
title_short | Circular RNA 0000096 affects cell growth and migration in gastric cancer |
title_sort | circular rna 0000096 affects cell growth and migration in gastric cancer |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5344286/ https://www.ncbi.nlm.nih.gov/pubmed/28081541 http://dx.doi.org/10.1038/bjc.2016.451 |
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