Evidence map›Paper›PMID 26316103›Full record

ArticleScientific reports2015

Up-regulation of Serum MiR-130b-3p Level is Associated with Renal Damage in Early Lupus Nephritis.

Wanpeng Wang, Shan Mou, Ling Wang, Minfang Zhang, Xinghua Shao, Wei Fang, Renhua Lu, Chaojun Qi, Zhuping Fan, Qin Cao and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 3 pooled it
2.7field-weighted citation impact, top 10% 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

34 citing papers in PubMed, 3 syntheses or guidelines pooled it, 71 citations in OpenAlex.

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  11. Polyamines from myeloid-derived suppressor cells promote Th17 polarization and disease progression.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
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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

13 authors at 1 institution in 1 country.

Wanpeng WangDepartment of Nephrology, Renji Hospital, School of Medicine, Shanghai Jiaotong University.
Shan MouDepartment of Nephrology, Renji Hospital, School of Medicine, Shanghai Jiaotong University.
Ling WangDepartment of Nephrology, Renji Hospital, School of Medicine, Shanghai Jiaotong University.
Minfang ZhangDepartment of Nephrology, Renji Hospital, School of Medicine, Shanghai Jiaotong University.
Xinghua ShaoDepartment of Nephrology, Renji Hospital, School of Medicine, Shanghai Jiaotong University.
Wei FangDepartment of Nephrology, Renji Hospital, School of Medicine, Shanghai Jiaotong University.
Renhua LuDepartment of Nephrology, Renji Hospital, School of Medicine, Shanghai Jiaotong University.
Chaojun QiDepartment of Nephrology, Renji Hospital, School of Medicine, Shanghai Jiaotong University.
Zhuping FanDepartment of Health Care center, Renji Hospital, School of Medicine, Shanghai Jiaotong University.
Qin CaoDepartment of Health Care center, Renji Hospital, School of Medicine, Shanghai Jiaotong University.
Qin WangDepartment of Nephrology, Renji Hospital, School of Medicine, Shanghai Jiaotong University.
Yan FangDepartment of Nephrology, Renji Hospital, School of Medicine, Shanghai Jiaotong University.
Zhaohui NiDepartment of Nephrology, Renji Hospital, School of Medicine, Shanghai Jiaotong University.
Renji Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systemic lupus erythematosus (SLE) is a common but severe autoimmune systemic inflammatory disease. Lupus nephritis (LN) is a serious complication of SLE,affecting up to 70% of SLE patients. Circulating microRNAs (miRNA) are emerging as biomarkers for pathological conditions and play significant roles in intercellular communication. In present research, serum samples from healthy control, early and late stage LN patients were used to analyze the expression profile of miRNAs by microarray. Subsequent study demonstrated that miR-130b-3p in serum of patients with early stage LN were significantly up-regulated when compared with healthy controls. In addition,we have also observed that the expression of a large amount of circulating microRNAs significantly decreased in patients with late stage LN. The further analysis found that the expression of serum miR-130b-3p was positively correlated with 24-hour proteinuria and renal chronicity index in patients with early stage LN.Transfection of renal tubular cellline(HK-2)with miR-130b-3p mimics can promote epithelial-mesenchymal transition (EMT). The opposite effects were observed when transfected with miR-130b-3p inhibitors. MiR-130b-3p negatively regulated ERBB2IP expression by directly targeting the 3'-UTR of ERBB2IP The circulating miR-130b-3p might serve as a biomarker and play an important role in renal damage in early stage LN patients.

Indexed as

Up-RegulationAdaptor Proteins, Signal TransducingAdultCell LineEpithelial CellsEpithelial-Mesenchymal TransitionFemaleGene Expression ProfilingHumansKidneyKidney TubulesLupus Erythematosus, SystemicLupus NephritisMaleMicroRNAsReproducibility of ResultsAdaptor Proteins, Signal TransducingERBIN protein, humanMicroRNAsMIRN-1233 microRNA, humanMIRN130 microRNA, humanTransforming Growth Factor beta1

Identifiers

PMID26316103
PMCPMC4551961
OpenAlexW2409180880

What OpenQuestion holds

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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 OpenQuestion graph.