Evidence map›Paper›PMID 30418172›Full record

ArticleThe Journal of clinical investigation2018

A protective role for microRNA-688 in acute kidney injury.

Nicholas Chun, Steven G Coca, John Cijiang He

Abstract readComment
In one paragraph

Article in The Journal of clinical investigation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

  1. Article
  2. Review
  3. Unique miRomics Expression Profiles inInternational journal of molecular sciences · 2023
    Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Nicholas ChunDepartment of Medicine/Nephrology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Steven G CocaDepartment of Medicine/Nephrology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
John Cijiang HeDepartment of Medicine/Nephrology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.

Funding

Complement Dependent Inflammation and Murine Heart Transplant RejectionK08AI135101 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CHUN, NICHOLAS · 2018 to 2022
$951k
6 · The paper itself

Abstract

Ischemia-reperfusion (I/R) sets off a devastating cascade of events, leading to cell death and possible organ failure. Treatments to limit I/R-associated damage are lacking, and the pathways that drive injury are poorly understood. In this issue of the JCI, Wei and colleagues identify microRNA-668 (miR-668) as a protective factor in acute kidney injury (AKI). miR-668 was shown to repress mitochondrial fission-associated protein MTP18, thereby inhibiting pathogenic mitochondrial fragmentation. In murine models of I/R-induced AKI, treatment with a miR-668 mimetic reduced mitochondrial fragmentation and improved renal function. Moreover, HIF-1α was shown to be required for miR-688 expression in response to I/R. Importantly, Wei et al. show miR-668 upregulation in a cohort of human patients with AKI. Together, these results identify a HIF-1α/miR-668/MTP18 axis that may have potential as a therapeutic target for AKI.

Indexed as

Acute Kidney InjuryMicroRNAsReperfusion InjuryAnimalsApoptosisHumansMiceMitochondrial DynamicsMitochondrial ProteinsMicroRNAsMitochondrial ProteinsMTFP1 protein, human

Identifiers

PMID30418172
PMCPMC6264641

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.