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Upregulation of circ_0066444 promotes the proliferation, invasion, and migration of gastric cancer cells
BACKGROUND: Circular RNAs (circRNAs), which have closed-loop structure, are involved in the pathogenesis of human diseases including various types of carcinomas. The present study aimed to investigate the relationship between a new circular RNA named circ_0066444 and gastric cancer (GC) carcinogenes...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5955026/ https://www.ncbi.nlm.nih.gov/pubmed/29785124 http://dx.doi.org/10.2147/OTT.S156516 |
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author | Rong, Dawei Dong, Chaoxi Fu, Kai Wang, Hanjin Tang, Weiwei Cao, Hongyong |
author_facet | Rong, Dawei Dong, Chaoxi Fu, Kai Wang, Hanjin Tang, Weiwei Cao, Hongyong |
author_sort | Rong, Dawei |
collection | PubMed |
description | BACKGROUND: Circular RNAs (circRNAs), which have closed-loop structure, are involved in the pathogenesis of human diseases including various types of carcinomas. The present study aimed to investigate the relationship between a new circular RNA named circ_0066444 and gastric cancer (GC) carcinogenesis. MATERIALS AND METHODS: The circ_0066444 levels in 106 paired gastric carcinoma tissues and related adjacent normal tissues were detected by real-time quantitative reverse-transcription polymerase chain reaction. The correlation between the expression of circ_0066444 and clinicopathological features was analyzed. The impact of circ_0066444 expression on cell proliferation, invasion, as well as migration was evaluated in vitro using knockdown expression strategies. Finally, a network of circ_0066444-targeted miRNA interactions and their corresponding mRNAs was constructed. RESULTS: circ_0066444 was found to be significantly upregulated in 106 GC tissues as compared with paired adjacent nontumorous tissues (P=0.025), showing a high positive correlation with lymphatic metastasis (P=0.023). Furthermore, in vitro assays of the GC cell lines BGC-823 and AGS demonstrated that knockdown of circ_0066444 reduced cell proliferation, invasion, and migration significantly. Prediction and annotation revealed circ_0066444 was able to sponge to 5 miRNAs and 15 corresponding target mRNAs. CONCLUSION: Our study indicated upregulation of circ_0066444 promotes gastric cell proliferation, invasion, and migration ability and might serve as a novel biomarker for GC. |
format | Online Article Text |
id | pubmed-5955026 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-59550262018-05-21 Upregulation of circ_0066444 promotes the proliferation, invasion, and migration of gastric cancer cells Rong, Dawei Dong, Chaoxi Fu, Kai Wang, Hanjin Tang, Weiwei Cao, Hongyong Onco Targets Ther Original Research BACKGROUND: Circular RNAs (circRNAs), which have closed-loop structure, are involved in the pathogenesis of human diseases including various types of carcinomas. The present study aimed to investigate the relationship between a new circular RNA named circ_0066444 and gastric cancer (GC) carcinogenesis. MATERIALS AND METHODS: The circ_0066444 levels in 106 paired gastric carcinoma tissues and related adjacent normal tissues were detected by real-time quantitative reverse-transcription polymerase chain reaction. The correlation between the expression of circ_0066444 and clinicopathological features was analyzed. The impact of circ_0066444 expression on cell proliferation, invasion, as well as migration was evaluated in vitro using knockdown expression strategies. Finally, a network of circ_0066444-targeted miRNA interactions and their corresponding mRNAs was constructed. RESULTS: circ_0066444 was found to be significantly upregulated in 106 GC tissues as compared with paired adjacent nontumorous tissues (P=0.025), showing a high positive correlation with lymphatic metastasis (P=0.023). Furthermore, in vitro assays of the GC cell lines BGC-823 and AGS demonstrated that knockdown of circ_0066444 reduced cell proliferation, invasion, and migration significantly. Prediction and annotation revealed circ_0066444 was able to sponge to 5 miRNAs and 15 corresponding target mRNAs. CONCLUSION: Our study indicated upregulation of circ_0066444 promotes gastric cell proliferation, invasion, and migration ability and might serve as a novel biomarker for GC. Dove Medical Press 2018-05-11 /pmc/articles/PMC5955026/ /pubmed/29785124 http://dx.doi.org/10.2147/OTT.S156516 Text en © 2018 Rong et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Rong, Dawei Dong, Chaoxi Fu, Kai Wang, Hanjin Tang, Weiwei Cao, Hongyong Upregulation of circ_0066444 promotes the proliferation, invasion, and migration of gastric cancer cells |
title | Upregulation of circ_0066444 promotes the proliferation, invasion, and migration of gastric cancer cells |
title_full | Upregulation of circ_0066444 promotes the proliferation, invasion, and migration of gastric cancer cells |
title_fullStr | Upregulation of circ_0066444 promotes the proliferation, invasion, and migration of gastric cancer cells |
title_full_unstemmed | Upregulation of circ_0066444 promotes the proliferation, invasion, and migration of gastric cancer cells |
title_short | Upregulation of circ_0066444 promotes the proliferation, invasion, and migration of gastric cancer cells |
title_sort | upregulation of circ_0066444 promotes the proliferation, invasion, and migration of gastric cancer cells |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5955026/ https://www.ncbi.nlm.nih.gov/pubmed/29785124 http://dx.doi.org/10.2147/OTT.S156516 |
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