Evidence map›Paper›PMID 25159851›Full record

ReviewPhysiological genomics2014

miR-21 in ischemia/reperfusion injury: a double-edged sword?

Xialian Xu, Alison J Kriegel, Xiaoyan Jiao, Hong Liu, Xiaowen Bai, Jessica Olson, Mingyu Liang, Xiaoqiang Ding

Abstract readReview
In one paragraph

Review in Physiological genomics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

67 citing papers in PubMed, 110 citations in OpenAlex.

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7 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

8 authors at 3 institutions in 2 countries.

Xialian XuDivision of Nephrology, Fudan University Zhongshan Hospital, Shanghai, Peoples Republic of China;
Alison J KriegelDepartment of Physiology, Medical College of Wisconsin, Milwaukee, Wisconsin;
Xiaoyan JiaoDivision of Nephrology, Fudan University Zhongshan Hospital, Shanghai, Peoples Republic of China;
Hong LiuDivision of Nephrology, Fudan University Zhongshan Hospital, Shanghai, Peoples Republic of China;
Xiaowen BaiDepartment of Anesthesiology, Medical College of Wisconsin, Milwaukee, Wisconsin;
Jessica OlsonDepartment of Physiology, Medical College of Wisconsin, Milwaukee, Wisconsin;
Mingyu LiangDepartment of Physiology, Medical College of Wisconsin, Milwaukee, Wisconsin;
Xiaoqiang DingDivision of Nephrology, Fudan University Zhongshan Hospital, Shanghai, Peoples Republic of China; Institutes of Biomedical Sciences of Shanghai Medical School, Fudan University, Shanghai, Peoples Republic of China; Kidney and Dialysis Institute of Shanghai, Shanghai, Peoples Republic of China; and Kidney and Blood Purification Laboratory of Shanghai, Shanghai, Peoples Republic of China ding.xiaoqiang@zs-hospital.sh.cn.
Medical College of Wisconsin · USFudan University · CNShanghai Blood Center · CN

Funding

Research ServicesP01HL082798 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI COWLEY, ALLEN W · 2006 to 2015
$22.0M
Clincal and Translational Science AwardUL1TR000055 · NCATS · MEDICAL COLLEGE OF WISCONSIN · PI SHAKER, REZA NONE · 2012 to 2015
$11.3M
microRNAs and Anesthetic-Induced Developmental NeurotoxicityR01GM112696 · NIGMS · MEDICAL COLLEGE OF WISCONSIN · PI BAI, XIAOWEN · 2014 to 2022
$3.0M
NCATS NIH HHS 8UL1TR-000055NCATS NIH HHS UL1 TR000055NHLBI NIH HHS HL-082798NHLBI NIH HHS HL-111580NHLBI NIH HHS HL-116264NHLBI NIH HHS P01 HL082798NIGMS NIH HHS R01 GM112696
6 · The paper itself

Abstract

MicroRNAs (miRNAs or miRs) are endogenous, small RNA molecules that suppress expression of targeted mRNA. miR-21, one of the most extensively studied miRNAs, is importantly involved in divergent pathophysiological processes relating to ischemia/reperfusion (I/R) injury, such as inflammation and angiogenesis. The role of miR-21 in renal I/R is complex, with both protective and pathological pathways being regulated by miR-21. Preconditioning-induced upregulation of miR-21 contributes to the protection against subsequent renal I/R injury through the targeting of genes such as the proapoptotic gene programmed cell death 4 and interactions between miR-21 and hypoxia-inducible factor. Conversely, long-term elevation of miR-21 may be detrimental to the organ by promoting the development of renal interstitial fibrosis following I/R injury. miR-21 is importantly involved in several pathophysiological processes related to I/R injury including inflammation and angiogenesis as well as the biology of stem cells that could be used to treat I/R injury; however, the effect of miR-21 on these processes in renal I/R injury remains to be studied.

Indexed as

AnimalsCell SurvivalFibrosisGene Expression RegulationHumansHypoxiaInflammationIschemiaIschemic PreconditioningKidneyMicroRNAsNeovascularization, PhysiologicReperfusion InjuryStem Cell TransplantationMicroRNAsMIRN21 microRNA, humanMIRN21 microRNA, mouseangiogenesisapoptosishypoxiainflammationmicroRNA

Identifiers

PMID25159851
PMCPMC4280148
OpenAlexW2059646584

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.