Evidence map›Paper›PMID 32182218›Full record

ArticleJCI insight2020

Interstitial microRNA miR-214 attenuates inflammation and polycystic kidney disease progression.

Ronak Lakhia, Matanel Yheskel, Andrea Flaten, Harini Ramalingam, Karam Aboudehen, Silvia Ferrè, Laurence Biggers, Abheepsa Mishra, Christopher Chaney, Darren P Wallace and 3 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
8.5field-weighted citation impact, top 2% 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

33 citing papers in PubMed, 63 citations in OpenAlex.

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  13. MicroRNAs in kidney injury and disease.Nature reviews. Nephrology · 2022
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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 4 institutions in 1 country.

Ronak LakhiaDepartment of Internal Medicine, University of Texas (UT) Southwestern Medical Center, Dallas, Texas, USA.
Matanel YheskelDepartment of Internal Medicine, University of Texas (UT) Southwestern Medical Center, Dallas, Texas, USA.
Andrea FlatenDepartment of Internal Medicine, University of Texas (UT) Southwestern Medical Center, Dallas, Texas, USA.
Harini RamalingamDepartment of Internal Medicine, University of Texas (UT) Southwestern Medical Center, Dallas, Texas, USA.
Karam AboudehenDepartment of Medicine, University of Minnesota School of Medicine, Minneapolis, Minnesota, USA.
Silvia FerrèDepartment of Internal Medicine, University of Texas (UT) Southwestern Medical Center, Dallas, Texas, USA.
Laurence BiggersDepartment of Internal Medicine, University of Texas (UT) Southwestern Medical Center, Dallas, Texas, USA.
Abheepsa MishraDepartment of Internal Medicine, University of Texas (UT) Southwestern Medical Center, Dallas, Texas, USA.
Christopher ChaneyDepartment of Internal Medicine, University of Texas (UT) Southwestern Medical Center, Dallas, Texas, USA.
Darren P WallaceDepartment of Medicine and the Jared Grantham Kidney Institute, University of Kansas Medical Center, Kansas City, Kansas, USA.
Thomas CarrollDepartment of Internal Medicine, University of Texas (UT) Southwestern Medical Center, Dallas, Texas, USA.
Peter IgarashiDepartment of Medicine, University of Minnesota School of Medicine, Minneapolis, Minnesota, USA.
Vishal PatelDepartment of Internal Medicine, University of Texas (UT) Southwestern Medical Center, Dallas, Texas, USA.
Southwestern Medical CenterSouthwestern Medical Center · USUniversity of Minnesota · USUniversity of Kansas Medical Center · US

Funding

UT Southwestern O'Brien Kidney Research Core CenterP30DK079328 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI MOE, ORSON W · 2007 to 2021
$16.9M
Engineering erythropoietin-producing cellsR24DK106743 · NIDDK · ROGOSIN INSTITUTE · PI CARROLL, THOMAS JOSEPH, CLEAVER, ONDINE B · 2015 to 2019
$7.0M
Pilot and Feasibility CoreP30DK106912 · NIDDK · UNIVERSITY OF KANSAS MEDICAL CENTER · PI CALVET, JAMES P · 2015 to 2019
$5.5M
The impact of RNA chemical modifications on polycystic kidney disease progressionR01DK102572 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI PATEL, VISHAL · 2015 to 2024
$3.5M
Interactions between the stroma and progenitor cells during kidney developmentR01DK095057 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI CARROLL, THOMAS JOSEPH · 2013 to 2016
$1.4M
The Role of Peroxisome Proliferator Activated Receptor Alpha in Autosomal Dominant Polycystic Kidney DiseaseK08DK117049 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI LAKHIA, RONAK · 2018 to 2022
$770k
NIDDK NIH HHS K08 DK117049NIDDK NIH HHS P30 DK079328NIDDK NIH HHS P30 DK106912NIDDK NIH HHS R01 DK095057NIDDK NIH HHS R01 DK102572NIDDK NIH HHS R24 DK106743
6 · The paper itself

Abstract

Renal cysts are the defining feature of autosomal dominant polycystic kidney disease (ADPKD); however, the substantial interstitial inflammation is an often-overlooked aspect of this disorder. Recent studies suggest that immune cells in the cyst microenvironment affect ADPKD progression. Here we report that microRNAs (miRNAs) are new molecular signals in this crosstalk. We found that miR-214 and its host long noncoding RNA Dnm3os are upregulated in orthologous ADPKD mouse models and cystic kidneys from humans with ADPKD. In situ hybridization revealed that interstitial cells in the cyst microenvironment are the primary source of miR-214. While genetic deletion of miR-214 does not affect kidney development or homeostasis, surprisingly, its inhibition in Pkd2- and Pkd1-mutant mice aggravates cyst growth. Mechanistically, the proinflammatory TLR4/IFN-γ/STAT1 pathways transactivate the miR-214 host gene. miR-214, in turn as a negative feedback loop, directly inhibits Tlr4. Accordingly, miR-214 deletion is associated with increased Tlr4 expression and enhanced pericystic macrophage accumulation. Thus, miR-214 upregulation is a compensatory protective response in the cyst microenvironment that restrains inflammation and cyst growth.

Indexed as

Signal TransductionAnimalsInflammationMiceMice, TransgenicMicroRNAsPolycystic Kidney, Autosomal DominantMicroRNAsMirn214 microRNA, mouseMonogenic diseasesNephrologyNoncoding RNAs

Identifiers

PMID32182218
PMCPMC7205276
OpenAlexW3010843717

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.