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Identification of potential biomarkers for SLE through mRNA expression profiling
Sara Kamal Rizk1, Amal Alhosary2, Enas S Zahran3
1Medical Biochemistry and Molecular Biology, Faculty of Medicine, Menoufia University, Shebin Elkom, Egypt.
Systemic lupus erythematosus (SLE) is linked to higher furin and NLRP3 gene expression and lower tristetraprolin (TTP) expression. These changes correlate with disease activity in SLE patients.
Area of Science:
- Immunology
- Molecular Biology
- Genetics
Background:
- Systemic lupus erythematosus (SLE) is a complex autoimmune disorder affecting multiple organ systems.
- Furin, tristetraprolin (TTP), and NOD, LRR, and pyrin domain-containing protein 3 (NLRP3) are implicated in the pathogenesis of autoimmune diseases.
Purpose of the Study:
- To investigate the role of furin, TTP, and NLRP3 mRNA gene expression in the pathogenesis and prognosis of Systemic Lupus Erythematosus (SLE).
Main Methods:
- A case-control study involving 210 participants (105 SLE cases, 105 controls).
- Real-time quantitative PCR was employed to measure mRNA gene expression levels of furin, TTP, and NLRP3 in all subjects.
Main Results:
- SLE patients exhibited significantly elevated serum furin and NLRP3 mRNA expression compared to controls (p < 0.001 and p = 0.006, respectively).
- Conversely, TTP mRNA expression was significantly lower in SLE patients than in controls (p < 0.001).
- Elevated furin and NLRP3 levels, along with decreased TTP levels, were associated with increased SLE disease activity.
Conclusions:
- Furin and NLRP3 gene expression are upregulated in SLE and correlate positively with disease activity.
- TTP gene expression is downregulated in SLE and shows a negative correlation with disease activity.
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