Evidence map›Paper›PMID 24441869›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2014

Let-7d microRNA affects mesenchymal phenotypic properties of lung fibroblasts.

Luai Huleihel, Ahmi Ben-Yehudah, Jadranka Milosevic, Guoying Yu, Kusum Pandit, Koji Sakamoto, Hanadie Yousef, Megan LeJeune, Tiffany A Coon, Carrie J Redinger and 4 more

Abstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed, 1 pooled it
5.0field-weighted citation impact, top 4% 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

48 citing papers in PubMed, 1 synthesis or guideline pooled it, 82 citations in OpenAlex.

  1. A systematic review of overlapping microRNA patterns in systemic sclerosis and idiopathic pulmonary fibrosis.European respiratory review : an official journal of the European Respiratory Society · 2017
    Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. ADAR1 Isoforms RegulateInternational journal of molecular sciences · 2022
    Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Idiopathic Pulmonary Comorbidities and Mechanisms.International journal of inflammation · 2021
    Review
  17. More than a Genetic Code: Epigenetics of Lung Fibrosis.Molecular diagnosis & therapy · 2020
    Review
  18. Article
  19. Article
  20. 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

14 authors at 5 institutions in 2 countries.

Luai HuleihelYale Univ., School of Medicine, 300 Cedar St., TAC-441 South, New Haven, CT 06520. naftali.kaminski@yale.edu.
Ahmi Ben-Yehudah
Jadranka Milosevic
Guoying Yu
Kusum Pandit
Koji Sakamoto
Hanadie Yousef
Megan LeJeune
Tiffany A Coon
Carrie J Redinger
Lara Chensny
Ester Manor
Gerald Schatten
Naftali Kaminski
University of Pittsburgh · USYale University · USMagee-Womens Research Institute · USBen-Gurion University of the Negev · ILUniversity of Pittsburgh Medical Center · US

Funding

Molecular Phenotypes within and across disease boundaries in IPF and COPDR01HL095397 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KAMINSKI, NAFTALI, SHAPIRO, STEVEN D · 2008 to 2011
$3.0M
Modeling in vivo Protein-DNA Interactions from High-Throughput Data MP1/1R01LM009657 · NLM · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BENOS, PANAGIOTIS V, KAMINSKI, NAFTALI · 2007 to 2011
$2.5M
Gene networks beyond organ boundaries; heart, lung and pulmonary vascular diseaseU01HL108642 · NHLBI · YALE UNIVERSITY · PI AHMAD, FERHAAN, BENOS, PANAGIOTIS V · 2011 to 2014
$2.2M
NHLBI NIH HHS R01HL095397NHLBI NIH HHS U01 HL108642NHLBI NIH HHS U01HL108642NLM NIH HHS R01LM009657
6 · The paper itself

Abstract

MicroRNAs are small noncoding RNAs that inhibit protein expression. We have previously shown that the inhibition of the microRNA let-7d in epithelial cells caused changes consistent with epithelial-to-mesenchymal transition (EMT) both in vitro and in vivo. The aim of this study was to determine whether the introduction of let-7d into fibroblasts alters their mesenchymal properties. Transfection of primary fibroblasts with let-7d caused a decrease in expression of the mesenchymal markers α-smooth muscle actin, N-cadherin, fibroblast-specific protein-1, and fibronectin, as well as an increase in the epithelial markers tight junction protein-1 and keratin 19. Phenotypic changes were also present, including a delay in wound healing, reduced motility, and proliferation of fibroblasts following transfection. In addition, we examined the effects of transfection on fibroblast responsiveness to TGF-β, an important factor in many fibrotic processes such as lung fibrosis and found that let-7d transfection significantly attenuated high-mobility group-A2 protein induction by TGF-β. Our results indicate that administration of the epithelial microRNA let-7d can significantly alter the phenotype of primary fibroblasts.

Indexed as

Epithelial-Mesenchymal TransitionActinsCadherinsCalcium-Binding ProteinsCell MovementCell ProliferationCells, CulturedFibroblastsFibronectinsHMGA2 ProteinHMGB2 ProteinHumansIdiopathic Pulmonary FibrosisKeratin-19LungMicroRNAsACTA2 protein, humanActinsCadherinsCalcium-Binding ProteinsFibronectinsHMGA2 ProteinHMGB2 ProteinKeratin-19MicroRNAsmirnlet7 microRNA, humanS100A4 protein, humanS100 Calcium-Binding Protein A4SNAI1 protein, humanSnail Family Transcription FactorsTranscription FactorsTransforming Growth Factor betaZonula Occludens-1 Proteinepithelial-to-mesenchymal transitionfibrosishigh-mobility group-A2 proteinidiopathic pulmonary fibrosismicroRNASlugtransforming growth factor-β

Identifiers

PMID24441869
PMCPMC3949080
OpenAlexW2101577916

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.