LncRNASNHG12 regulates the development of diabetic nephropathy through miR-129-5p/IL6ST axis.

Authors

Liping Dong, Pengcheng Sun, Yutong Hu, Zihui Xu, Fei Xiong, Yuxin Xian

Published in

Molecular biology reports. Volume 53. Issue 1. Aug 11, 2026. Epub Aug 11, 2026.

Abstract

Diabetic Nephropathy (DN) pathogenesis remains incompletely understood.
This study aimed to explore the mechanistic function of long non-coding RNA (lncRNA) SNHG12 in the progression of DN.
In this study, 150 type 2 diabetes mellitus (T2DM) patients and 150 DN patients were recruited. Human kidney-2 (HK-2) cells were exposed to high glucose (HG) to establish a DN cell model. The target gene expression was assessed by reverse transcription quantitative real-time PCR (RT-qPCR), cell proliferation was evaluated using the Cell Counting Kit-8 (CCK-8) assay, cell apoptosis was determined by flow cytometry, inflammatory factor levels were measured by enzyme-linked immunosorbent assay (ELISA), and molecular interactions were confirmed through the RNA immunoprecipitation (RIP) and dual-luciferase reporter assay.
In DN patients, SNHG12 and interleukin 6 signal transducer (IL6ST) were significantly elevated, whereas miR-129-5p expression was down-regulated, indicating that SNHG12 may serve as a potential biomarker for the auxiliary diagnosis of DN. Multivariate regression analysis showed that SNHG12 was a risk factor for DN. Moreover, under HG conditions, silencing of SNHG12 promoted cell proliferation, inhibited apoptosis, and mitigated inflammatory responses, as well as attenuated fibrosis, reflected by decreased expression of transforming growth factor-beta 1 (TGF-β1) and alpha-smooth muscle actin (α-SMA). Furthermore, SNHG12 could directly bind to and regulate miR-129-5p, which in turn targeted the 3'UTR of IL6ST. Inhibition of miR-129-5p or overexpression of IL6ST partially reversed the protective effects of SNHG12 knockdown on cellular functions.
SNHG12 promoted the progression of DN by upregulating IL6ST expression through the sponging of miR-129-5p.

PMID:
42579189
Bibliographic data and abstract were imported from PubMed on 11 Aug 2026.

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