Evidence map›Paper›PMID 30715692›Full record

ArticleInflammation2019

MicroRNA-155 Mediates Obesity-Induced Renal Inflammation and Dysfunction.

Chenfei Zheng, Ji Zhang, Xinxin Chen, Jianna Zhang, Xiaokai Ding, Xiaohan You, Lin Fan, Chaosheng Chen, Ying Zhou

Abstract read
PubMed Publisher
In one paragraph

Article in Inflammation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.1field-weighted citation impact, top 28% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 26 citations in OpenAlex.

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  11. Role of microRNAs in Obesity-Related Kidney Disease.International journal of molecular sciences · 2021
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4 · The record

Corrections and comments

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

9 authors at 1 institution in 1 country.

Chenfei ZhengDepartment of Nephrology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, China.
Ji ZhangDepartment of Nephrology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, China.
Xinxin ChenDepartment of Nephrology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, China.
Jianna ZhangDepartment of Nephrology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, China.
Xiaokai DingDepartment of Nephrology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, China.
Xiaohan YouDepartment of Nephrology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, China.
Lin FanDepartment of Nephrology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, China.
Chaosheng ChenDepartment of Nephrology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, China. wzccs8@163.com.
Ying ZhouDepartment of Nephrology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, China. zhouying610@yeah.net.ORCID http://orcid.org/0000-0002-3614-2647
Wenzhou Medical University · CN

Funding

Guangzhou Science and Technology Project of China 20170420167Medical Science and Technology Foundation of Guangdong Province (CN) A2018042Wenzhou Committee of Science and Technology of China ZS2017008;Y20170055Zhejiang Province Natural Science Foundation LY16H150007Zhejiang Province Public Welfare Technology Application Research Project (CN) LY14H050006
6 · The paper itself

Abstract

Chronic inflammation is a major contributor to obesity-related renal damage. Recent studies have demonstrated that microRNA (miR)-155 is closely associated with hyperglycemia-induced nephropathy, but whether renal miR-155 participates in the inflammatory response and development of obesity-related nephropathy is unknown. In present study, we investigated the pathophysiological role of renal miR-155 in palmitic acid (PA)-treated endothelial cell and high-fat-diet (HFD)-fed mouse models by specific miR-155 sponge. Mice fed with HFD exhibited higher levels of renal miR-155, which positively correlated with urine microalbumin and blood urea nitrogen. In vitro study, mouse renal vascular endothelial cells stimulated with PA also showed higher miR-155 levels, accompanied with increased inflammatory response. Suppression of renal miR-155 effectively attenuated HFD-induced renal structural damages and dysfunction. MiR-155 sponge treatment also significantly decreased NF-κB signaling and downstream gene expression in vitro and in vivo. The obesity-increased macrophage infiltration and lipotoxicity was decreased in mouse kidney after miR-155 sponge treatment. Mechanistically, miR-155 directly targeted 3'-UTR of SHIP1/INPP5D and suppressed its expression in vitro and in vivo, whereas silence of SHIP1/INPP5D abolished the renal protective benefits of miR-155 sponge in obese mice. Taken together, present findings for the first time provided evidence for the potential role of miR-155 in obesity-related nephropathy and clarified that SHIP1/NF-κB signaling was a potential molecular mechanism.

Indexed as

AnimalsCell MovementDiet, High-FatInflammationKidney DiseasesMacrophagesMiceMicroRNAsNF-kappa BObesityPhosphatidylinositol-3,4,5-Trisphosphate 5-PhosphatasesSignal TransductionInpp5d protein, mouseMicroRNAsMirn155 microRNA, mouseNF-kappa BPhosphatidylinositol-3,4,5-Trisphosphate 5-PhosphatasesinflammationmiR-155nephropathyobesitySHIP1/INPP5D

Identifiers

PMID30715692
OpenAlexW2913244196

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 OpenQuestion graph.