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LncRNA Expression Profiles in Systemic Lupus Erythematosus and Rheumatoid Arthritis: Emerging Biomarkers and
Han Wu1, Shuxian Chen1, Aifen Li1
1Clinical Research Center, Department of Clinical Laboratory, Key Laboratory of Prevention and Management of Chronic Kidney Disease of Zhanjiang City, Affiliated Hospital of Guangdong Medical University, Zhanjiang, China.
Long non-coding RNAs (lncRNAs) are key in systemic lupus erythematosus (SLE) and rheumatoid arthritis (RA) pathogenesis. Dysregulated lncRNAs show promise as novel biomarkers and therapeutic targets for these autoimmune diseases.
Area of Science:
- Immunology
- Molecular Biology
- Genetics
Background:
- Systemic lupus erythematosus (SLE) and rheumatoid arthritis (RA) are common autoimmune diseases with overlapping features.
- Long non-coding RNAs (lncRNAs) are increasingly recognized for their role in autoimmune disease pathogenesis.
Purpose of the Study:
- To review the roles of lncRNAs as potential biomarkers and therapeutic targets in SLE and RA.
- To summarize current research on lncRNA dysregulation in these autoimmune conditions.
Main Methods:
- A narrative review of original articles on lncRNAs in SLE and RA published up to November 1, 2021.
- Analysis of lncRNA expression profiles in various biological samples (PBMCs, serum, exosomes).
Main Results:
- Several lncRNAs, including GAS5, NEAT1, TUG1, linc0949, and linc0597, are dysregulated in SLE.
- lncRNAs such as HOTAIR, GAS5, and HIX003209 are identified as promising biomarkers for RA diagnosis and treatment.
- Shared lncRNAs like GAS5 may influence SLE via the MAPK pathway and RA via the AMPK pathway.
Conclusions:
- lncRNAs represent a significant area of research for understanding SLE and RA pathogenesis.
- Specific lncRNAs hold potential as novel biomarkers for early diagnosis and effective therapeutic strategies in SLE and RA.
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