Evidence map›Paper›PMID 39512414›Full record

ArticleAdvanced biomedical research2024

Initial Evaluation of lncRNA A2M-AS1 Gene Expression in Multiple Sclerosis Patients.

Shaghayegh Mohammadi, Tahereh Sadeghiyan, Mohammad Rezaei, Mansoureh Azadeh

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Article in Advanced biomedical research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Shaghayegh MohammadiDepartment of Genetics, Faculty of Biology Sciences and Technology, Shahid Ashrafi Esfahani, Isfahan, Iran.
Tahereh SadeghiyanDepartment of Genetics, Faculty of Biology Sciences and Technology, Shahid Ashrafi Esfahani, Isfahan, Iran.
Mohammad RezaeiDepartment of Biology and Biotechnology, University of Pavia, Pavia, Italy.
Mansoureh AzadehZist Fanavari Novin Biotechnology Institute, Isfahan, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Multiple sclerosis (MS) is one of the three leading neurodegenerative diseases worldwide. Gene expression profile studies play an important role in recognizing and preventing disease. Considering the inherent ability of biomarkers to diagnose and prognose the occurrence of a disease, with the aim of gene therapy and changing gene expression, it can be helped to treat it. In this study, by examining the gene interaction and expression of non-coding genes in patients with MS, using bioinformatics analyses, laboratory research and potential non-coding diagnostic biomarkers of MS were selected for further investigations. Materials and Methods: First, by using micro-array data analysis of the GEO database, the expression status of the long non-coding ribonucleic acid (RNA) (lncRNA) A2M-AS1 gene was investigated in patients with MS. lncRNA-mRNA interaction analysis was performed in the lncRRisearch database. After sample collection, the total RNA extracted using the RNA extraction kit from 20 patient samples and 20 healthy samples was synthesized into cDNA with the synthesis kit. The quantitative reverse transcriptase polymerase chain reaction experiment was performed for the final validation of expression change. Results: Based on bioinformatic and laboratory analysis, the expression of the A2M-AS1 gene in MS samples showed a significant decrease in expression compared to healthy samples. Also, based on the receiver operating characteristic analysis, lncRNA A2M-AS1 can be introduced as an acceptable diagnostic biomarker to distinguish MS samples from healthy samples. Conclusion: lncRNA A2M-AS1, by reducing its expression as an acceptable diagnostic biomarker, can increase the risk of developing MS.

Indexed as

Biomarkersgene expression profilinglong non-coding RNAmultiple sclerosis

Identifiers

PMID39512414
PMCPMC11542686

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