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A Quantitative Detection Method for MicroRNAs in the Kidney of an Ischemic Kidney Injury Mouse Model
Published on: September 11, 2020
miR-7974 as a potential biomarker for lupus nephritis and its involvement in disease progression
Rongzheng Yue1, Shanshan Wang1, Jing Wang1
1Department of Nephrology, Kidney Research Institute, West China Hospital of Sichuan University, No. 37 Guoxue Lane, Wuhou District, Chengdu City, 610041, China.
Background:
Lupus nephritis (LN) is a prevalent and severe complication associated with systemic lupus erythematosus (SLE), posing a substantial risk to renal function and adversely affecting the quality of life of affected individuals. miRNAs play a crucial regulatory role in adaptive immune responses. However, the involvement of specific miRNAs in LN is rarely reported. This research aims to examine the clinical value of miR-7974, as well as the expression changes and interaction mechanisms of the miR-7974/DDAH1 axis in LN, and its impact on the pathogenesis of LN.
Methods:
The expression levels of miR-7974 and DDAH1 were measured using real-time fluorescence quantification. CCK-8 was utilized to assess cell proliferation ability. ELISA was employed to quantify the levels of inflammatory factors. The binding of miR-7974 to DDAH1 was verified using a dual luciferase reporter gene assay.
Results:
miR-7974 is highly expressed in blood samples from patients with LN and LPS-induced HRMCs, whereas DDAH1 is expressed at low levels. The ROC curve suggests that miR-7974 possesses diagnostic value. The knockdown of miR-7974 and the overexpression of DDAH1 both inhibit cell proliferation and reduce levels of inflammatory cytokines. Additionally, miR-7974 negatively regulates DDAH1.
Conclusions:
miR-7974 plays a role in the progression of LN by negatively regulating DDAH1. The miR-7974/DDAH1 axis may serve as a non-invasive biomarker and a potential therapeutic target for the diagnosis of LN.
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