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Circular RNA-Related CeRNA Network and Prognostic Signature for Patients with Osteosarcoma

INTRODUCTION: Osteosarcoma (OSA) is characterized by its relatively high morbidity in children and adolescents. Patients usually have advanced disease at the time of diagnosis, resulting in poor outcomes. This study focused on building a circular RNA-based ceRNA network to develop a reliable model f...

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Autores principales: Man, Gu, Duan, Ao, Liu, Wanshun, Cheng, Jiangqi, Liu, Yu, Song, Jiahang, Zhou, Haisen, Shen, Kai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8494289/
https://www.ncbi.nlm.nih.gov/pubmed/34629900
http://dx.doi.org/10.2147/CMAR.S328559
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author Man, Gu
Duan, Ao
Liu, Wanshun
Cheng, Jiangqi
Liu, Yu
Song, Jiahang
Zhou, Haisen
Shen, Kai
author_facet Man, Gu
Duan, Ao
Liu, Wanshun
Cheng, Jiangqi
Liu, Yu
Song, Jiahang
Zhou, Haisen
Shen, Kai
author_sort Man, Gu
collection PubMed
description INTRODUCTION: Osteosarcoma (OSA) is characterized by its relatively high morbidity in children and adolescents. Patients usually have advanced disease at the time of diagnosis, resulting in poor outcomes. This study focused on building a circular RNA-based ceRNA network to develop a reliable model for OSA risk prediction. METHODS: We used the Gene Expression Omnibus (GEO) datasets to explore the expression patterns of circRNA, miRNA, and mRNA in OSA. The prognostic value of circRNA host genes was assessed with data from the Therapeutically Applicable Research to Generate Effective Treatments (TARGET) database using Kaplan–Meier survival analysis. We established a circRNA-related ceRNA network and annotated its biological functions. Next, we developed a prognostic risk signature based on mRNAs extracted from the ceRNA network. We also developed a prognostic model and constructed a nomogram to enhance the prediction of OSA prognosis. RESULTS: We identified 166 DEcircRNAs, 233 DEmiRNAs, and 1317 DEmRNAs and used them to create a circRNA-related ceRNA network. We then established a prognostic risk model consisting of four genes (MLLT11, TNFRSF11B, SLC7A7, and PARVA). Moreover, we found that inhibition of MLLT11 and SLC7A7 blocked OSA cell proliferation and migration in in vitro experiments. CONCLUSION: Our study identifies crucial prognostic genes and provides a circRNA-related ceRNA network for OSA, which will contribute to the elucidation of the molecular mechanisms underlying the oncogenesis and development of OSA.
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spelling pubmed-84942892021-10-07 Circular RNA-Related CeRNA Network and Prognostic Signature for Patients with Osteosarcoma Man, Gu Duan, Ao Liu, Wanshun Cheng, Jiangqi Liu, Yu Song, Jiahang Zhou, Haisen Shen, Kai Cancer Manag Res Original Research INTRODUCTION: Osteosarcoma (OSA) is characterized by its relatively high morbidity in children and adolescents. Patients usually have advanced disease at the time of diagnosis, resulting in poor outcomes. This study focused on building a circular RNA-based ceRNA network to develop a reliable model for OSA risk prediction. METHODS: We used the Gene Expression Omnibus (GEO) datasets to explore the expression patterns of circRNA, miRNA, and mRNA in OSA. The prognostic value of circRNA host genes was assessed with data from the Therapeutically Applicable Research to Generate Effective Treatments (TARGET) database using Kaplan–Meier survival analysis. We established a circRNA-related ceRNA network and annotated its biological functions. Next, we developed a prognostic risk signature based on mRNAs extracted from the ceRNA network. We also developed a prognostic model and constructed a nomogram to enhance the prediction of OSA prognosis. RESULTS: We identified 166 DEcircRNAs, 233 DEmiRNAs, and 1317 DEmRNAs and used them to create a circRNA-related ceRNA network. We then established a prognostic risk model consisting of four genes (MLLT11, TNFRSF11B, SLC7A7, and PARVA). Moreover, we found that inhibition of MLLT11 and SLC7A7 blocked OSA cell proliferation and migration in in vitro experiments. CONCLUSION: Our study identifies crucial prognostic genes and provides a circRNA-related ceRNA network for OSA, which will contribute to the elucidation of the molecular mechanisms underlying the oncogenesis and development of OSA. Dove 2021-10-01 /pmc/articles/PMC8494289/ /pubmed/34629900 http://dx.doi.org/10.2147/CMAR.S328559 Text en © 2021 Man et al. https://creativecommons.org/licenses/by-nc/3.0/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/ (https://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. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Man, Gu
Duan, Ao
Liu, Wanshun
Cheng, Jiangqi
Liu, Yu
Song, Jiahang
Zhou, Haisen
Shen, Kai
Circular RNA-Related CeRNA Network and Prognostic Signature for Patients with Osteosarcoma
title Circular RNA-Related CeRNA Network and Prognostic Signature for Patients with Osteosarcoma
title_full Circular RNA-Related CeRNA Network and Prognostic Signature for Patients with Osteosarcoma
title_fullStr Circular RNA-Related CeRNA Network and Prognostic Signature for Patients with Osteosarcoma
title_full_unstemmed Circular RNA-Related CeRNA Network and Prognostic Signature for Patients with Osteosarcoma
title_short Circular RNA-Related CeRNA Network and Prognostic Signature for Patients with Osteosarcoma
title_sort circular rna-related cerna network and prognostic signature for patients with osteosarcoma
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8494289/
https://www.ncbi.nlm.nih.gov/pubmed/34629900
http://dx.doi.org/10.2147/CMAR.S328559
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