TY - JOUR
T1 - microRNA-Based Network and Pathway Analysis for Neuropathic Pain in Rodent Models
AU - Zheng, Yi Li
AU - Su, Xuan
AU - Chen, Yu Meng
AU - Guo, Jia Bao
AU - Song, Ge
AU - Yang, Zheng
AU - Chen, Pei Jie
AU - Wang, Xue Qiang
N1 - Publisher Copyright:
Copyright © 2022 Zheng, Su, Chen, Guo, Song, Yang, Chen and Wang.
PY - 2022/1/13
Y1 - 2022/1/13
N2 - Neuropathic pain (NP) is poorly managed, and in-depth mechanisms of gene transcriptome alterations in NP pathogenesis are not yet fully understood. To determine microRNA-related molecular mechanisms of NP and their transcriptional regulation in NP, PubMed, Embase, Web of Science and CINAHL Complete (EBSCO) were searched from inception to April 2021. Commonly dysregulated miRNAs in NP were assessed. The putative targets of these miRNAs were determined using TargetScan, Funrich, Cytoscape and String database. A total of 133 literatures containing miRNA profiles studies and experimentally verify studies were included. Venn analysis, target gene prediction analysis and functional enrichment analysis indicated several miRNAs (miR-200b-3p, miR-96, miR-182, miR-183, miR-30b, miR-155 and miR-145) and their target genes involved in known relevant pathways for NP. Targets on transient receptor potential channels, voltage-gated sodium channels and voltage-gated calcium channels may be harnessed for pain relief. A further delineation of signal processing and modulation in neuronal ensembles is key to achieving therapeutic success in future studies.
AB - Neuropathic pain (NP) is poorly managed, and in-depth mechanisms of gene transcriptome alterations in NP pathogenesis are not yet fully understood. To determine microRNA-related molecular mechanisms of NP and their transcriptional regulation in NP, PubMed, Embase, Web of Science and CINAHL Complete (EBSCO) were searched from inception to April 2021. Commonly dysregulated miRNAs in NP were assessed. The putative targets of these miRNAs were determined using TargetScan, Funrich, Cytoscape and String database. A total of 133 literatures containing miRNA profiles studies and experimentally verify studies were included. Venn analysis, target gene prediction analysis and functional enrichment analysis indicated several miRNAs (miR-200b-3p, miR-96, miR-182, miR-183, miR-30b, miR-155 and miR-145) and their target genes involved in known relevant pathways for NP. Targets on transient receptor potential channels, voltage-gated sodium channels and voltage-gated calcium channels may be harnessed for pain relief. A further delineation of signal processing and modulation in neuronal ensembles is key to achieving therapeutic success in future studies.
KW - bioinformatics analysis
KW - biomarker
KW - functional enrichment analysis
KW - miRNA
KW - neuropathic pain
UR - https://www.scopus.com/pages/publications/85123723893
U2 - 10.3389/fmolb.2021.780730
DO - 10.3389/fmolb.2021.780730
M3 - 文章
AN - SCOPUS:85123723893
SN - 2296-889X
VL - 8
JO - Frontiers in Molecular Biosciences
JF - Frontiers in Molecular Biosciences
M1 - 780730
ER -