Evidence map›Paper›PMID 24644282›Full record

ArticleThe Journal of biological chemistry2014

miR-17-92 cluster targets phosphatase and tensin homology and Ikaros Family Zinc Finger 4 to promote TH17-mediated inflammation.

Si-Qi Liu, Shan Jiang, Chaoran Li, Baojun Zhang, Qi-Jing Li

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed, 1 pooled it
6.4field-weighted citation impact, top 3% 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

95 citing papers in PubMed, 1 synthesis or guideline pooled it, 145 citations in OpenAlex.

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35 more citing papers are in PubMed but not listed here.

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

5 authors at 2 institutions in 1 country.

Si-Qi LiuFrom the Department of Immunology, Duke University Medical Center, Durham, North Carolina 27710.
Shan Jiang
Chaoran Li
Baojun Zhang
Qi-Jing Li
Duke University Hospital · USDuke Medical Center · US

Funding

Women's Cancer Research ProgramP30CA014236 · NCI · DUKE UNIVERSITY · PI DONNA NIEDZWIECKI · 1985 to 2026
$174.8M
Regulatory mechanisms of miR-19b, a novel mediator of T cell autoimmunityR01AI091878 · NIAID · DUKE UNIVERSITY · PI LI, QIJING · 2012 to 2016
$1.8M
Harnessing microRNAs within miR-17-92 cluster for autoimmune interventionR56AI091878 · NIAID · DUKE UNIVERSITY · PI LI, QIJING · 2011 to 2011
$384k
NCI NIH HHS P30 CA014236NIAID NIH HHS R01 AI091878NIAID NIH HHS R56 AI091878PHS HHS RAI091878APHS HHS RAI091878B
6 · The paper itself

Abstract

The miR-17-92 cluster regulates a broad spectrum of biological processes of T cell immunity. This cluster was found to facilitate T cell proliferation, enhance antitumor activities and promote T cell-dependent antibody responses. However, little is known about the role of this miRNA cluster in the development of autoimmune diseases. Multiple sclerosis is a neuro-destructive autoimmune disease caused by the pathogenicity of TH17 cells, whose differentiation is tightly controlled by a variety of transcriptional and post-transcriptional regulators. Our study unveils the critical role of miR-17-92 in TH17 differentiation: T cell-specific miR-17-92 deficiency reduced TH17 differentiation and ameliorated experimental autoimmune encephalomyelitis (EAE) symptoms. We demonstrated that miR-17 and miR-19b are the two miRNAs in this cluster responsible for promoting TH17 responses. MiR-19b represses the expression of Phosphatase and Tensin Homology (PTEN), thereby augmenting the PI3K-AKT-mTOR axis essential for proper TH17 differentiation. Meanwhile, miR-17 enhances TH17 polarization by inhibiting a novel target, Ikaros Family Zinc Finger 4 (IKZF4). By establishing the miR-17-92 cluster as a key driver of TH17 responses, our data identify this miRNA cluster as a potential therapeutic target for the clinical intervention of multiple sclerosis.

Indexed as

AnimalsBlotting, WesternCarrier ProteinsCell DifferentiationCells, CulturedColitisDisease Models, AnimalDNA-Binding ProteinsEncephalomyelitis, Autoimmune, ExperimentalFlow CytometryGene Expression RegulationIkaros Transcription FactorInflammationMiceMice, Inbred C57BLMice, KnockoutCarrier ProteinsDNA-Binding ProteinsIkaros Transcription FactorMicroRNAsMIRN17-92 microRNA, mouseMirn17 microRNA, mouseMIRN19 microRNA, mouseNerve Tissue ProteinsPTEN PhosphohydrolasePten protein, mouseZfpn1a4 protein, mouseAutoimmunityCell DifferentiationIKZF4InflammationMicroRNAmiR-17-92PtenT CellTh17

Identifiers

PMID24644282
PMCPMC4007439
OpenAlexW2000316267

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.