Evidence map›Paper›PMID 26303294›Full record

ReviewDrug development research2015

Alteration of Aging-Dependent MicroRNAs in Idiopathic Pulmonary Fibrosis.

Richard Seonghun Nho

Open access · hybridAbstract readReview
In one paragraph

Review in Drug development research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

14 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Investigating Matrix-Fibroblast Regulation of MicroRNAs. A Dice(r)y Proposition.American journal of respiratory and critical care medicine · 2018
    Article
  13. Review
  14. Epithelial to mesenchymal transition-related proteins ZEB1, β-catenin, and β-tubulin-III in idiopathic pulmonary fibrosis.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2017
    Article
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

1 author at 1 institution in 1 country.

Richard Seonghun NhoDepartment of Medicine, University of Minnesota, Minneapolis, MN, 55455, USA.
University of Minnesota · US

Funding

Pathological alteration of FoxO3a in IPF pathogenesisR01HL114662 · NHLBI · UNIVERSITY OF MINNESOTA · PI NHO, RICHARD S. · 2013 to 2016
$1.5M
NHLBI NIH HHS R01 HL114662
6 · The paper itself

Abstract

Preclinical Research Idiopathic Pulmonary Fibrosis (IPF) is the most severe fibrotic lung disease and characterized by the accumulation of (myo)fibroblasts and collagen within the alveolar wall resulting in obliteration of the gas-exchange surface. Although the detailed pathogenesis is not understood, recent studies have found that several microRNAs (miRNAs) are associated with the progression of lung diseases including IPF. IPF is a fibrotic disease and, most frequently found in an aged population. In this review, the functional roles of miRNAs that are deregulated in IPF progression are discussed together with how aging affects the miRNA signature, altering the fibroblast phenotype and promoting lung fibrosis. Finally, the possibility of targeting miRNAs as a therapeutic approach for the treatment of IPF is discussed.

Indexed as

AgingHumansIdiopathic Pulmonary FibrosisMicroRNAsModels, GeneticMolecular Targeted TherapyMicroRNAsagingidiopathic pulmonary fibrosismicroRNAreactive oxygen species

Identifiers

PMID26303294
PMCPMC4615542
OpenAlexW1831442459

What OpenQuestion holds

Textmetadata
LicenceTDM
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.