Long Non-Coding RNAs, Novel Offenders or Guardians in Multiple Sclerosis: A Scoping Review.


Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2021
Historique:
received: 10 09 2021
accepted: 08 11 2021
entrez: 24 12 2021
pubmed: 25 12 2021
medline: 11 2 2022
Statut: epublish

Résumé

Multiple sclerosis (MS), a chronic inflammatory demyelinating disease of the central nervous system, is one of the most common neurodegenerative diseases worldwide. MS results in serious neurological dysfunctions and disability. Disturbances in coding and non-coding genes are key components leading to neurodegeneration along with environmental factors. Long non-coding RNAs (lncRNAs) are long molecules in cells that take part in the regulation of gene expression. Several studies have confirmed the role of lncRNAs in neurodegenerative diseases such as MS. In the current study, we performed a systematic analysis of the role of lncRNAs in this disorder. In total, 53 studies were recognized as eligible for this systematic review. Of the listed lncRNAs, 52 lncRNAs were upregulated, 37 lncRNAs were downregulated, and 11 lncRNAs had no significant expression difference in MS patients compared with controls. We also summarized some of the mechanisms of lncRNA functions in MS. The emerging role of lncRNAs in neurodegenerative diseases suggests that their dysregulation could trigger neuronal death

Identifiants

pubmed: 34950142
doi: 10.3389/fimmu.2021.774002
pmc: PMC8688805
doi:

Substances chimiques

Biomarkers 0
RNA, Long Noncoding 0

Types de publication

Journal Article Meta-Analysis Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

774002

Informations de copyright

Copyright © 2021 Jalaiei, Asadi, Sabaie, Dehghani, Gharesouran, Hussen, Taheri, Ghafouri-Fard and Rezazadeh.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Abbas Jalaiei (A)

Molecular Medicine Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Department of Medical Genetics, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.

Mohammad Reza Asadi (MR)

Molecular Medicine Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

Hani Sabaie (H)

Molecular Medicine Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Department of Medical Genetics, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.

Hossein Dehghani (H)

Department of Molecular Medicine, School of Medicine, Birjand University of Medical Sciences, Birjand, Iran.

Jalal Gharesouran (J)

Department of Medical Genetics, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.

Bashdar Mahmud Hussen (BM)

Department Pharmacognosy, College of Pharmacy, Hawler Medical University, Erbil, Iraq.

Mohammad Taheri (M)

Skull Base Research Center, Loghman Hakim Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Institute of Human Genetics, Jena University Hospital, Jena, Germany.

Soudeh Ghafouri-Fard (S)

Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Maryam Rezazadeh (M)

Molecular Medicine Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Department of Medical Genetics, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.

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