pmid: 31721530,   nlmid 101566618,  doi:10.22074/cellj.2020.6555

Evaluation of The Expression Levels of Three Long Non-Coding RNAs in Multiple Sclerosis.


Moradi, Afshin Rahimi Naiini, Mahdis Yazdanpanahi, Nasrin Tabatabaeian, Hossein Nabatchian, Fariba Baghi, Masoud Azadeh, Mansoureh Ghaedi, Kamran

Vol. 22, Issue 22, Jul.2020

Cell journal (Cell J),  ISSN 2228-5806

Abstract

Multiple sclerosis (MS) is a chronic disorder involving both inflammatory and neurodegenerative responses. Long non-coding RNAs (lncRNAs) have been had an emerging role as the biomarkers of different disorders, including autoimmune diseases. Previous studies have shown that NR_003531.3 (MEG3a), AC000061.1_201, and AC007182.6 play a role in the pathogenesis of human autoimmune diseases. However, the potential significance of these lncRNAs, as the diagnostic biomarkers of MS, has not been studied yet. We aimed to quantitatively evaluate the expression levels of NR_003531.3, AC000061.1_201, and AC007182.6 in peripheral blood samples of MS patients in comparison with healthy controls. In this case-control study, the blood samples from 20 MS patients and 10 healthy controls were collected. Total RNA was extracted, and the expression levels of three selected lncRNAs were quantitatively measured using the quantitative real time-polymerase chain reaction (qRT-PCR) method. We detected a significant down-regulation in the expression of NR_003531.3 in MS patients, while no marked changes were observed in the expression of AC000061.1_201 and AC007182.6 in patients compared with controls. Based on the receiver operating characteristic (ROC) curve analysis, NR_003531.3 could discriminate MS patients from healthy subjects effectively. Regarding the prognosis of MS patients, NR_003531.3 is significantly and inversely correlated with the expanded disability status scale (EDSS). The potential role of NR_003531.3 lncRNA as a diagnostic biomarker to distinguish MS patients is proposed. Prognostically, NR_003531.3 correlates with lower disability rates in MS patients.


MESH Headings


Article Keywords

Autoimmune Disease | Gene Expression Profiling | Long Non-coding RNA | Multiple Sclerosis | Neurodegenerative Disease |


Chemical

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