Evidence map›Paper›PMID 36674762›Full record

ArticleInternational journal of molecular sciences2023

Phenotypic Alteration of an Established Human Airway Cell Line by Media Selection.

Galit Livnat, Jessica D Meeker, Alicia J Ostmann, Lauren M Strecker, John P Clancy, John J Brewington

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. 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

6 authors at 3 institutions in 2 countries.

Galit LivnatPediatric Pulmonology and CF Center, Carmel Medical Center, Haifa 3100000, Israel.ORCID 0000-0003-3132-7746
Jessica D MeekerDepartment of Pediatrics, College of Medicine, University of Cincinnati, Cincinnati, OH 45299, USA.
Alicia J OstmannDepartment of Pediatrics, College of Medicine, University of Cincinnati, Cincinnati, OH 45299, USA.
Lauren M StreckerDepartment of Pediatrics, College of Medicine, University of Cincinnati, Cincinnati, OH 45299, USA.
John P ClancyCystic Fibrosis Foundation, Bethesda, MD 20810, USA.
John J BrewingtonDepartment of Pediatrics, College of Medicine, University of Cincinnati, Cincinnati, OH 45299, USA.
Cincinnati Children's Hospital Medical Center · USCystic Fibrosis Foundation · USTechnion – Israel Institute of Technology · IL

Funding

Cystic Fibrosis Foundation CLANCY14XX0Cystic Fibrosis Foundation CLANCY15R0
6 · The paper itself

Abstract

Cystic Fibrosis (CF) is caused by mutations in the CF transmembrane conductance regulator (CFTR), a chloride/bicarbonate channel. Many studies utilize human airway cell models (cell lines and primary cells) to study different aspects of CFTR biology. Media selection can alter the growth and differentiation of primary cells, yet the impact on stable airway cell lines is unclear. To determine the impact of media and growth conditions on CFBE41o- cells stably transduced with wild-type or F508del CFTR, we examined four commonly used growth media, measuring epithelial and mesenchymal markers, as well as CFTR expression, maturation, and function. The selection of growth media altered the expression of epithelial and mesenchymal markers in the cell lines, and significantly impacted CFTR expression and subsequent function. These results highlight the importance of media selection to CFTR and cell line behavior and should be considered in both studies of primary human airway cells and stable cell lines.

Indexed as

Cystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorCell LineEpithelial CellsHumansMutationCystic Fibrosis Transmembrane Conductance RegulatorCFBE41o-CFTRcystic fibrosisgrowth mediatissue culture

Identifiers

PMID36674762
PMCPMC9862772
OpenAlexW4313824358

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.