Integrated Analysis of Mutations, miRNA and mRNA Expression in Glioblastoma
ShiChao Wang,1 HuanMin Zhou,1 RuiJian Zhang,2 YanRu Zhang1 1College of Life Sciences, Inner Mongolia Agricultural University, Hohhot, Inner Mongolia, 010018, People’s Republic of China; 2Department of Neurosurgery, The People’s Hospital of Inner Mongolia, Hohhot, Inner Mongolia, 010017, People’s Rep...
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2021
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oai:doaj.org-article:87f4ecc137aa4d4a85e1f90ac39a4e2b2021-11-16T18:47:50ZIntegrated Analysis of Mutations, miRNA and mRNA Expression in Glioblastoma1178-7074https://doaj.org/article/87f4ecc137aa4d4a85e1f90ac39a4e2b2021-11-01T00:00:00Zhttps://www.dovepress.com/integrated-analysis-of-mutations-mirna-and-mrna-expression-in-glioblas-peer-reviewed-fulltext-article-IJGMhttps://doaj.org/toc/1178-7074ShiChao Wang,1 HuanMin Zhou,1 RuiJian Zhang,2 YanRu Zhang1 1College of Life Sciences, Inner Mongolia Agricultural University, Hohhot, Inner Mongolia, 010018, People’s Republic of China; 2Department of Neurosurgery, The People’s Hospital of Inner Mongolia, Hohhot, Inner Mongolia, 010017, People’s Republic of ChinaCorrespondence: YanRu Zhang Tel +976 18047183314Email mdmzhh_2008@126.comBackground: Glioblastoma multiforme (GBM) is a common, malignant brain tumor in adults, with a median survival of only 15– 23 months. Organisms respond to disease stress through sophisticated mechanisms at the physiological, transcriptional and metabolic levels. However, the molecular regulatory networks responsible for occurrence, progression and recurrence of glioma have yet to be elucidated.Methods: In this study, we sought to determine the cause of gliomas by developing an RNA-seq technique that analyzes mRNA and small RNA (sRNA) with the aim of discovering potential methods for precisely blocking key signaling pathways in occurrence, progression, and recurrence. The explication of mechanisms leading to GBM formation has become a feasible and promising new therapeutic method.Results: GBM-associated genes were identified based on their expression during the disease stress response. Analysis of the inverse correlations between microRNAs (miRNAs) and target mRNAs revealed 43 mRNA–miRNA interactions during disease progression. BOC-SMO and BOC-RAS were found to promote the malignant progression of glioma. A total of 3088 differentially expressed genes were identified as involved in several biological processes, such as amino acid metabolism, protein transport associated with immune response, cell proliferation, and cell apoptosis. Fifteen miRNAs were also identified as being differentially expressed in GBM and control groups.Conclusion: The results of this study provide an important foundation for understanding the pathogenesis of glioma and discovering new therapeutic targets.Keywords: glioblastoma multiforme, transcriptome, miRNAWang SZhou HZhang RZhang YDove Medical Pressarticleglioblastoma multiformetranscriptomemirnaMedicine (General)R5-920ENInternational Journal of General Medicine, Vol Volume 14, Pp 8281-8292 (2021) |
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glioblastoma multiforme transcriptome mirna Medicine (General) R5-920 |
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glioblastoma multiforme transcriptome mirna Medicine (General) R5-920 Wang S Zhou H Zhang R Zhang Y Integrated Analysis of Mutations, miRNA and mRNA Expression in Glioblastoma |
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ShiChao Wang,1 HuanMin Zhou,1 RuiJian Zhang,2 YanRu Zhang1 1College of Life Sciences, Inner Mongolia Agricultural University, Hohhot, Inner Mongolia, 010018, People’s Republic of China; 2Department of Neurosurgery, The People’s Hospital of Inner Mongolia, Hohhot, Inner Mongolia, 010017, People’s Republic of ChinaCorrespondence: YanRu Zhang Tel +976 18047183314Email mdmzhh_2008@126.comBackground: Glioblastoma multiforme (GBM) is a common, malignant brain tumor in adults, with a median survival of only 15– 23 months. Organisms respond to disease stress through sophisticated mechanisms at the physiological, transcriptional and metabolic levels. However, the molecular regulatory networks responsible for occurrence, progression and recurrence of glioma have yet to be elucidated.Methods: In this study, we sought to determine the cause of gliomas by developing an RNA-seq technique that analyzes mRNA and small RNA (sRNA) with the aim of discovering potential methods for precisely blocking key signaling pathways in occurrence, progression, and recurrence. The explication of mechanisms leading to GBM formation has become a feasible and promising new therapeutic method.Results: GBM-associated genes were identified based on their expression during the disease stress response. Analysis of the inverse correlations between microRNAs (miRNAs) and target mRNAs revealed 43 mRNA–miRNA interactions during disease progression. BOC-SMO and BOC-RAS were found to promote the malignant progression of glioma. A total of 3088 differentially expressed genes were identified as involved in several biological processes, such as amino acid metabolism, protein transport associated with immune response, cell proliferation, and cell apoptosis. Fifteen miRNAs were also identified as being differentially expressed in GBM and control groups.Conclusion: The results of this study provide an important foundation for understanding the pathogenesis of glioma and discovering new therapeutic targets.Keywords: glioblastoma multiforme, transcriptome, miRNA |
format |
article |
author |
Wang S Zhou H Zhang R Zhang Y |
author_facet |
Wang S Zhou H Zhang R Zhang Y |
author_sort |
Wang S |
title |
Integrated Analysis of Mutations, miRNA and mRNA Expression in Glioblastoma |
title_short |
Integrated Analysis of Mutations, miRNA and mRNA Expression in Glioblastoma |
title_full |
Integrated Analysis of Mutations, miRNA and mRNA Expression in Glioblastoma |
title_fullStr |
Integrated Analysis of Mutations, miRNA and mRNA Expression in Glioblastoma |
title_full_unstemmed |
Integrated Analysis of Mutations, miRNA and mRNA Expression in Glioblastoma |
title_sort |
integrated analysis of mutations, mirna and mrna expression in glioblastoma |
publisher |
Dove Medical Press |
publishDate |
2021 |
url |
https://doaj.org/article/87f4ecc137aa4d4a85e1f90ac39a4e2b |
work_keys_str_mv |
AT wangs integratedanalysisofmutationsmirnaandmrnaexpressioninglioblastoma AT zhouh integratedanalysisofmutationsmirnaandmrnaexpressioninglioblastoma AT zhangr integratedanalysisofmutationsmirnaandmrnaexpressioninglioblastoma AT zhangy integratedanalysisofmutationsmirnaandmrnaexpressioninglioblastoma |
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1718426252218466304 |