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Expression analysis of mTOR-associated lncRNAs in multiple sclerosis
Mohammadarian Akbari1, Fatemeh Eshghyar2, Mahdi Gholipour3
1Phytochemistry Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Metabolic Brain Disease
|May 27, 2022
Summary
This study found that two mTOR-related long non-coding RNAs (lncRNAs), SNHG5 and DANCR, are down-regulated in multiple sclerosis (MS) patients, suggesting their role in MS pathophysiology.
Area of Science:
- Immunology
- Molecular Biology
- Genetics
Background:
- The mechanistic target of rapamycin (mTOR) pathway regulates immune cell differentiation and immune responses.
- mTOR is implicated in autoimmune disorders like multiple sclerosis (MS).
- Long non-coding RNAs (lncRNAs) are increasingly recognized for their roles in complex diseases.
Purpose of the Study:
- To investigate the expression levels of mTOR and four associated lncRNAs (SNHG1, SNHG3, SNHG5, DANCR) in peripheral blood of MS patients.
- To explore the correlation between gene expression and clinical/demographic data in MS.
- To assess the diagnostic potential of these lncRNAs in distinguishing MS patients from healthy controls.
Main Methods:
- Real-time quantitative polymerase chain reaction (RT-qPCR) was used to measure gene expression.
- Peripheral blood samples were collected from patients with MS and healthy controls.
- Statistical analyses were performed to assess gene expression differences, correlations, and diagnostic accuracy (AUC).
Main Results:
- Down-regulation of SNHG5 and DANCR was observed in MS patients compared to controls.
- A significant negative correlation was found between mTOR gene expression and MS disease duration.
- SNHG5 and DANCR showed good (AUC=0.88) and moderate (AUC=0.68) diagnostic potential, respectively.
Conclusions:
- The study suggests the involvement of mTOR-related lncRNAs, specifically SNHG5 and DANCR, in the pathophysiology of multiple sclerosis.
- These lncRNAs may serve as potential biomarkers for MS.
- Further research is warranted to elucidate the precise mechanisms of these lncRNAs in MS pathogenesis.
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