MiRNA-29a serves as a promising diagnostic biomarker in children with temporal lobe epilepsy and regulates seizure-induced cell death and inflammation in hippocampal neurons (notice n° 611692)

détails MARC
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control field 20250121162618.0
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Language code of text/sound track or separate title fre
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100 10 - MAIN ENTRY--PERSONAL NAME
Personal name Wu, Yifei
Relator term author
245 00 - TITLE STATEMENT
Title MiRNA-29a serves as a promising diagnostic biomarker in children with temporal lobe epilepsy and regulates seizure-induced cell death and inflammation in hippocampal neurons
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Date of publication, distribution, etc. 2021.<br/>
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General note 85
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Summary, etc. ObjectiveTemporal lobe epilepsy (TLE) in children is one of the most common refractory epilepsies. MicroRNAs (miRNAs) show abnormal expression in neurological disorders. The objective of this study was to determine changes in expression and the role of miR-29a in children with TLE. MethodsSixty-five TLE patients and 70 normal controls were recruited. The levels of miR-29a were quantified using qRT-PCR. An in vitro TLE cell model was established using primary hippocampal cells cultured in magnesium-free medium. Cell viability, cell apoptosis and inflammatory cytokine concentrations were evaluated. The luciferase reporter assay was applied to confirm the target gene, HMGB1. ResultsA low level of MiR-29a expression was observed in the serum of children with TLE, which demonstrated a negative association with the concentration of serum TNF-α, IL-6, and IFN-γ. The level of MiR-29a demonstrated high specificity and sensitivity in children with TLE. A low level of expression of miR-29a was also detected in the TLE cell model. MiR-29a over-expression reversed the decreased cell viability induced by TLE, and alleviated cell apoptosis. Release of TNF-α, IL-6, and IFN-γ induced by TLE was also inhibited by miR-29a over-expression. HMGB1, which was downregulated in the serum of TLE patients, was shown to be a target gene of miR-29a, and negatively correlated with miR-29a level. SignificanceThe downregulation of serum miR-29a may serve as a non-invasive diagnostic biomarker for children with TLE. MiR-29a may be involved in the pathogenesis of TLE through regulation of neuronal apoptosis and neuroinflammation via targeting HMGB1.
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element temporal lobe epilepsy
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Topical term or geographic name as entry element hippocampus neuron
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element miR-29a
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Topical term or geographic name as entry element neuroinflammation
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Topical term or geographic name as entry element HMGB1
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Zhang, Yanrui
Relator term author
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Zhu, Shuxia
Relator term author
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Tian, Chunmei
Relator term author
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Zhang, Yanyan
Relator term author
786 0# - DATA SOURCE ENTRY
Note Epileptic Disorders | Vol 23 | 6 | 2021-06-01 | p. 823-832 | 1294-9361
856 41 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://shs.cairn.info/revue-epileptic-disorders-2021-6-page-823?lang=en&redirect-ssocas=7080">https://shs.cairn.info/revue-epileptic-disorders-2021-6-page-823?lang=en&redirect-ssocas=7080</a>

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