Evidence map›Paper›PMID 30152192›Full record

ArticleInternational forum of allergy & rhinology2019

Resveratrol and ivacaftor are additive G551D CFTR-channel potentiators: therapeutic implications for cystic fibrosis sinus disease.

Do-Yeon Cho, Shaoyan Zhang, Ahmed Lazrak, Jessica W Grayson, Jaime A Peña Garcia, Daniel F Skinner, Dong Jin Lim, Calvin Mackey, Catherine Banks, Sadis Matalon and 1 more

Abstract read
In one paragraph

Article in International forum of allergy & rhinology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

12 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Observational
  6. Review
  7. Antibiotic eluting sinus stents.Laryngoscope investigative otolaryngology · 2020
    Review
  8. Review
  9. Resveratrol restores intracellular transport in cystic fibrosis epithelial cells.American journal of physiology. Lung cellular and molecular physiology · 2020
    Article
  10. Article
  11. Mutation-specific dual potentiators maximize rescue of CFTR gating mutants.Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society · 2020
    Article
  12. Review
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

11 authors at 1 institution in 1 country.

Do-Yeon ChoDepartment of Otolaryngology, University of Alabama at Birmingham, Birmingham, AL.
Shaoyan ZhangDepartment of Otolaryngology, University of Alabama at Birmingham, Birmingham, AL.
Ahmed LazrakGregory Fleming James Cystic Fibrosis Research Center, University of Alabama at Birmingham, Birmingham, AL.
Jessica W GraysonDepartment of Otolaryngology, University of Alabama at Birmingham, Birmingham, AL.
Jaime A Peña GarciaDepartment of Otolaryngology, University of Alabama at Birmingham, Birmingham, AL.
Daniel F SkinnerDepartment of Otolaryngology, University of Alabama at Birmingham, Birmingham, AL.
Dong Jin LimDepartment of Otolaryngology, University of Alabama at Birmingham, Birmingham, AL.
Calvin MackeyDepartment of Otolaryngology, University of Alabama at Birmingham, Birmingham, AL.
Catherine BanksDepartment of Otolaryngology, University of Alabama at Birmingham, Birmingham, AL.
Sadis MatalonGregory Fleming James Cystic Fibrosis Research Center, University of Alabama at Birmingham, Birmingham, AL.
Bradford A WoodworthDepartment of Otolaryngology, University of Alabama at Birmingham, Birmingham, AL.
University of Alabama at Birmingham · US

Funding

UAB CF Research and Translation Core CenterP30DK072482 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Brian R. Davis · 2007 to 2026
$23.0M
Translational Program in CFTR-Related Airway DiseasesR35HL135816 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI ROWE, STEVEN MARK · 2017 to 2022
$6.3M
Ivacaftor for Acquired CFTR Dysfunction in Chronic RhinosinusitisR01HL133006 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI WOODWORTH, BRADFORD ALAN · 2016 to 2020
$1.7M
NHLBI NIH HHS R01 HL133006NHLBI NIH HHS R35 HL135816NIDDK NIH HHS P30 DK072482
6 · The paper itself

Abstract

backgroundMutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene result in defective Cl

methodsFisher rat thyroid cells (FRT) transfected with G551D CFTR and human sinonasal epithelial cells (HSNE) containing the CFTR G551D mutation were subjected to pharmacologic manipulation of transepithelial ion transport in Ussing chambers. Activity was further evaluated using whole-cell patch clamp methods in G551D FRT cells.

resultsIn G551D FRT cells, resveratrol (100 μM) and ivacaftor (10 μM) significantly increased Cl

conclusionAdditive improvement in G551D CFTR-mediated Cl

Indexed as

AminophenolsAnimalsCells, CulturedChloridesCystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorDrug SynergismDrug Therapy, CombinationHumansIon TransportMucociliary ClearanceMutationNasal MucosaParanasal Sinus DiseasesQuinolonesRatsAminophenolsCFTR protein, humanChloridesCystic Fibrosis Transmembrane Conductance RegulatorivacaftorQuinolonesResveratrolCFTRCFTR potentiatorchronic rhinosinusitischronic sinusitiscystic fibrosisG551Divacaftormucociliary clearanceresveratrolsinusitis

Identifiers

PMID30152192
PMCPMC6318032
OpenAlexW2889277879

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.