Evidence map›Paper›PMID 41199154›Full record

ArticleBMC nephrology2025

miR-7974 as a potential biomarker for lupus nephritis and its involvement in disease progression.

Rongzheng Yue, Shanshan Wang, Jing Wang, Hongyu Qiu

Abstract read
In one paragraph

Article in BMC nephrology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Rongzheng YueDepartment of Nephrology, Kidney Research Institute, West China Hospital of Sichuan University, No. 37 Guoxue Lane, Wuhou District, Chengdu City, 610041, China.
Shanshan WangDepartment of Nephrology, Kidney Research Institute, West China Hospital of Sichuan University, No. 37 Guoxue Lane, Wuhou District, Chengdu City, 610041, China.
Jing WangDepartment of Nephrology, Kidney Research Institute, West China Hospital of Sichuan University, No. 37 Guoxue Lane, Wuhou District, Chengdu City, 610041, China.
Hongyu QiuDepartment of Nephrology, Kidney Research Institute, West China Hospital of Sichuan University, No. 37 Guoxue Lane, Wuhou District, Chengdu City, 610041, China. Qhy250717@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLupus 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.

methodsThe 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.

resultsmiR-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.

conclusionsmiR-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.

Indexed as

AmidohydrolasesLupus NephritisMicroRNAsAdultBiomarkersCell ProliferationDisease ProgressionFemaleHumansMaleAmidohydrolasesBiomarkersdimethylargininaseMicroRNAsDDAH1Lupus nephritismiR-7974Potential biomarker

Identifiers

PMID41199154
PMCPMC12590879

What Socratic holds

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.