Evidence map›Paper›PMID 33657462›Full record

ArticleMolecular immunology2021

HIF-1α and miR-210 differential and lineage-specific expression in systemic lupus erythematosus.

Barry Garchow, Yvan Maque Acosta, Marianthi Kiriakidou

Open access · hybridAbstract read
In one paragraph

Article in Molecular immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 17% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

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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

3 authors at 1 institution in 1 country.

Barry GarchowDepartment of Medicine, Division of Rheumatology, Sidney Kimmel Medical College, Thomas Jefferson University, 211 S. 9(th)St. Suite 210, Philadelphia, PA 19107, USA.
Yvan Maque AcostaDepartment of Medicine, Division of Rheumatology, Sidney Kimmel Medical College, Thomas Jefferson University, 211 S. 9(th)St. Suite 210, Philadelphia, PA 19107, USA.
Marianthi KiriakidouDepartment of Medicine, Division of Rheumatology, Sidney Kimmel Medical College, Thomas Jefferson University, 211 S. 9(th)St. Suite 210, Philadelphia, PA 19107, USA. Electronic address: marianthi.kiriakidou@jefferson.edu.
Thomas Jefferson University · US

Funding

Effects of miR-21 and miR-155 inhibition in SLER21AR063416 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI KIRIAKIDOU, MARIANTHI · 2013 to 2014
$368k
Characterization of microRNA-regulated signaling pathways in mouse SLER03AR060988 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI KIRIAKIDOU, MARIANTHI · 2011 to 2013
$272k
NIAMS NIH HHS R03 AR060988NIAMS NIH HHS R21 AR063416
6 · The paper itself

Abstract

Systemic lupus erythematosus (SLE, lupus) is a chronic autoimmune disease characterized by loss of peripheral tolerance to nuclear self-antigens. It is increasingly recognized that aberrant T cell metabolism is a critical mediator of SLE immunopathology. Hypoxia inducible factor 1⍺ (HIF-1α) is a key transcription factor that regulates T cell metabolism in response to immune stimuli. T cell activation induces HIF-1α expression and transcriptional activation of HIF-responsive genes. HypoxamiRs are a group of microRNAs sensitive to HIF-1α transcriptional regulation that function to fine-tune the HIF-driven transcriptional program. The 'master' hypoxamiR, miR-210 is transcriptionally regulated by HIF-1α and negatively regulates HIF-1α activity. Although a key role for HIF-1α in has been described in a number of autoimmune and inflammatory diseases and abnormal microRNA expression profiles correlate with poor clinical outcome in a number of rheumatologic diseases, the expression and function of HIF-1α and miR-210 in lupus remains largely uncharacterized. Here we report HIF-1α and miR-210 differential and lineage-specific expression in systemic lupus erythematosus. We show that HIF-1α mRNA and protein is overexpressed in human lupus CD4

Indexed as

AnimalsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesForkhead Transcription FactorsGene Expression RegulationHumansHypoxia-Inducible Factor 1, alpha SubunitLupus Erythematosus, SystemicLymphocyte ActivationMiceMice, Inbred C57BLMicroRNAsNuclear Receptor Subfamily 1, Group F, Member 3Forkhead Transcription FactorsFOXP3 protein, humanHIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitMicroRNAsMIRN210 microRNA, humanNuclear Receptor Subfamily 1, Group F, Member 3RORC protein, humanAutoimmune diseaseCD4HIF-1αIL-17LupusLymphocytesmicroRNAmiR-210PBMCSLET cellTCRTh17

Identifiers

PMID33657462
PMCPMC8026684
OpenAlexW3135335565

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.