Evidence mapPaperPMID 42135680Full record

ArticleBMC endocrine disorders2026

Hsa-miR-5585-3p regulates the NLRP3 activation and the expression of cytokines through CHUK in a cellular model of diabetic kidney disease.

Jing Zeng, Xuexiang Qin, Jielian Wang, Cunyou Xiong, Xiaoyun Feng

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Article in BMC endocrine disorders, 2026. 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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5 authors.

Jing Zeng *Department of Nephrology, Shulan (Hangzhou) Hospital, Hangzhou, 310000, China.
Xuexiang Qin *Department of Rheumatology and Immunology, The First Hospital of Kunming, Kunming, 650034, China.
Jielian WangDepartment of Nephrology, Tianyou Hospital, Wuhan University of Science and Technology, Wuhan, 430064, China.
Cunyou XiongDepartment of General Medicine, Minkang Community Health Center, Shenzhen Longhua District People's Hospital, Minzhi street, Shenzhen, Guangdong, 518131, China. xiongxunyou7532@163.com.
Xiaoyun FengDepartment of Endocrinology and Metabolism, Jiading Branch of Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, No. 800, Huangjiahuayuan Road, Jiading District, Shanghai, 201803, China. Fengxiaoyundr@163.com.

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6 · The paper itself

Abstract

backgroundApproximately 20-40% of patients with diabetes mellitus (DM) develop diabetic kidney disease (DKD), a major microvascular complication of the condition. This study aimed to explore the potential diagnostic value of hsa-miR-5585-3p for DKD, and its regulatory effects, by targeting CHUK, on inflammatory factor expression and NLRP3 activation in HK-2 cells induced by high glucose (HG).

methodsThe expression profile of hsa-miR-5585-3p in the serum samples from patients with type 2 DM (T2DM) and DKD was analyzed by RT-qPCR. Correlation analysis between hsa-miR-5585-3p and UACR, eGFR, as well as inflammatory factors was investigated. Bioinformatics analysis predicted the downstream target genes of hsa-miR-5585-3p. The interaction between hsa-miR-5585-3p and CHUK was verified by dual luciferase reporter assay. An in vitro DKD model was established by exposing HK-2 cells to HG. The expression levels of inflammatory factors and the NLRP3 activation were detected by RT-qPCR, Western blot, or ELISA following modulation of the hsa-miR-5585-3p/CHUK axis.

resultsHsa-miR-5585-3p was significantly downregulated in the serum of DKD patients and showed correlations with UACR, eGFR, and inflammatory factors. In HK-2 cells stimulated by HG, hsa-miR-5585-3p suppressed the expression of inflammatory factors as well as key molecules in the NLRP3 pathway. Data from the rescue experiment supported the partial role of CHUK overexpression in counteracting the inhibition mediated by hsa-miR-5585-3p.

conclusionsHsa-miR-5585-3p may serve as a potential diagnostic biomarker for DKD, pending further validation. Moreover, hsa-miR-5585-3p regulated the inflammatory response and activation of the NLRP3 in HK-2 cells induced by HG through CHUK. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

CytokinesDiabetes Mellitus, Type 2Diabetic NephropathiesMicroRNAsNLR Family, Pyrin Domain-Containing 3 ProteinCell LineFemaleHumansMaleMiddle AgedCytokinesMicroRNAsNLR Family, Pyrin Domain-Containing 3 ProteinNLRP3 protein, humanCHUKDiabetic kidney diseaseHsa-miR-5585-3pInflammatory responseNLRP3 pathway

Identifiers

PMID42135680
PMCPMC13343648

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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.