Integrative network analysis of N<sup>6</sup> methylation-related genes reveal potential therapeutic targets for spinal cord injury

The diagnosis of the severity of spinal cord injury (SCI) and the revelation of potential therapeutic targets are crucial for urgent clinical care and improved patient outcomes. Here, we analyzed the overall gene expression data in peripheral blood leukocytes during the acute injury phase collected...

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Autores principales: Shanzheng Wang, Xinhui Xie, Chao Li, Jun Jia, Changhong Chen
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Lenguaje:EN
Publicado: AIMS Press 2021
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Acceso en línea:https://doaj.org/article/d9d6a821bcf74fad98ad6a3cc1fcb3db
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spelling oai:doaj.org-article:d9d6a821bcf74fad98ad6a3cc1fcb3db2021-11-24T01:01:46ZIntegrative network analysis of N<sup>6</sup> methylation-related genes reveal potential therapeutic targets for spinal cord injury10.3934/mbe.20214051551-0018https://doaj.org/article/d9d6a821bcf74fad98ad6a3cc1fcb3db2021-09-01T00:00:00Zhttps://www.aimspress.com/article/doi/10.3934/mbe.2021405?viewType=HTMLhttps://doaj.org/toc/1551-0018The diagnosis of the severity of spinal cord injury (SCI) and the revelation of potential therapeutic targets are crucial for urgent clinical care and improved patient outcomes. Here, we analyzed the overall gene expression data in peripheral blood leukocytes during the acute injury phase collected from Gene Expression Omnibus (GEO) and identified six m6A regulators specifically expressed in SCI compared to normal samples. LncRNA-mRNA network analysis identified AKT2/3 and PIK3R1 related to m6A methylation as potential therapeutic targets for SCI and constructed a classifier to identify patients of SCI to assist clinical diagnosis. Moreover, FTO (eraser) and RBMX (reader) were found to be significantly down-regulated in SCI and the functional gene co-expressed with them was found to be involved in the signal transduction of multiple pathways related to nerve injury. Through the construction of the drug-target gene network, eight key genes were identified as drug targets and it was emphasized that fostamatinib can be used as a potential drug for the treatment of SCI. Taken together, our study characterized the pathogenesis and identified a potential therapeutic target of SCI providing theoretical support for the development of precision medicine.Shanzheng WangXinhui XieChao LiJun JiaChanghong Chen AIMS Pressarticlen<sup>6</sup> methylationspinal cord injurylncrnatherapeutic targetsnetwork analysisBiotechnologyTP248.13-248.65MathematicsQA1-939ENMathematical Biosciences and Engineering, Vol 18, Iss 6, Pp 8174-8187 (2021)
institution DOAJ
collection DOAJ
language EN
topic n<sup>6</sup> methylation
spinal cord injury
lncrna
therapeutic targets
network analysis
Biotechnology
TP248.13-248.65
Mathematics
QA1-939
spellingShingle n<sup>6</sup> methylation
spinal cord injury
lncrna
therapeutic targets
network analysis
Biotechnology
TP248.13-248.65
Mathematics
QA1-939
Shanzheng Wang
Xinhui Xie
Chao Li
Jun Jia
Changhong Chen
Integrative network analysis of N<sup>6</sup> methylation-related genes reveal potential therapeutic targets for spinal cord injury
description The diagnosis of the severity of spinal cord injury (SCI) and the revelation of potential therapeutic targets are crucial for urgent clinical care and improved patient outcomes. Here, we analyzed the overall gene expression data in peripheral blood leukocytes during the acute injury phase collected from Gene Expression Omnibus (GEO) and identified six m6A regulators specifically expressed in SCI compared to normal samples. LncRNA-mRNA network analysis identified AKT2/3 and PIK3R1 related to m6A methylation as potential therapeutic targets for SCI and constructed a classifier to identify patients of SCI to assist clinical diagnosis. Moreover, FTO (eraser) and RBMX (reader) were found to be significantly down-regulated in SCI and the functional gene co-expressed with them was found to be involved in the signal transduction of multiple pathways related to nerve injury. Through the construction of the drug-target gene network, eight key genes were identified as drug targets and it was emphasized that fostamatinib can be used as a potential drug for the treatment of SCI. Taken together, our study characterized the pathogenesis and identified a potential therapeutic target of SCI providing theoretical support for the development of precision medicine.
format article
author Shanzheng Wang
Xinhui Xie
Chao Li
Jun Jia
Changhong Chen
author_facet Shanzheng Wang
Xinhui Xie
Chao Li
Jun Jia
Changhong Chen
author_sort Shanzheng Wang
title Integrative network analysis of N<sup>6</sup> methylation-related genes reveal potential therapeutic targets for spinal cord injury
title_short Integrative network analysis of N<sup>6</sup> methylation-related genes reveal potential therapeutic targets for spinal cord injury
title_full Integrative network analysis of N<sup>6</sup> methylation-related genes reveal potential therapeutic targets for spinal cord injury
title_fullStr Integrative network analysis of N<sup>6</sup> methylation-related genes reveal potential therapeutic targets for spinal cord injury
title_full_unstemmed Integrative network analysis of N<sup>6</sup> methylation-related genes reveal potential therapeutic targets for spinal cord injury
title_sort integrative network analysis of n<sup>6</sup> methylation-related genes reveal potential therapeutic targets for spinal cord injury
publisher AIMS Press
publishDate 2021
url https://doaj.org/article/d9d6a821bcf74fad98ad6a3cc1fcb3db
work_keys_str_mv AT shanzhengwang integrativenetworkanalysisofnsup6supmethylationrelatedgenesrevealpotentialtherapeutictargetsforspinalcordinjury
AT xinhuixie integrativenetworkanalysisofnsup6supmethylationrelatedgenesrevealpotentialtherapeutictargetsforspinalcordinjury
AT chaoli integrativenetworkanalysisofnsup6supmethylationrelatedgenesrevealpotentialtherapeutictargetsforspinalcordinjury
AT junjia integrativenetworkanalysisofnsup6supmethylationrelatedgenesrevealpotentialtherapeutictargetsforspinalcordinjury
AT changhongchen integrativenetworkanalysisofnsup6supmethylationrelatedgenesrevealpotentialtherapeutictargetsforspinalcordinjury
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