Evidence map›Paper›PMID 42744679›Full record

ReviewJournal of cystic fibrosis : official journal of the European Cystic Fibrosis Society2026

Epigenetic regulation and chromatin organization in cystic fibrosis airways.

Agustín De Ganzó, Brian Chan, Michael Rubinstein, Kenichi Okuda, Carla M P Ribeiro

Abstract readReview
In one paragraph

Review in Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Agustín De GanzóMarsico Lung Institute and Cystic Fibrosis Center, University of North Carolina at Chapel Hill, NC, USA.
Brian ChanThomas Lord Department of Mechanical Engineering and Materials Science, Duke University, Durham, NC, USA. Electronic address: brian.chan@duke.edu.
Michael RubinsteinMarsico Lung Institute and Cystic Fibrosis Center, University of North Carolina at Chapel Hill, NC, USA; Thomas Lord Department of Mechanical Engineering and Materials Science, Duke University, Durham, NC, USA; Departments of Biomedical Engineering, Chemistry, and Physics, Duke University, Durham, NC, USA; Institute for Chemical Reaction Design and Discovery (WPI-ICReDD), Hokkaido University, Sapporo, Japan.
Kenichi OkudaMarsico Lung Institute and Cystic Fibrosis Center, University of North Carolina at Chapel Hill, NC, USA; Department of Medicine, University of North Carolina at Chapel Hill, NC, USA.
Carla M P RibeiroMarsico Lung Institute and Cystic Fibrosis Center, University of North Carolina at Chapel Hill, NC, USA; Department of Medicine, University of North Carolina at Chapel Hill, NC, USA; Department of Cell Biology and Physiology, University of North Carolina at Chapel Hill, NC, USA.

Funding

Project 4: Biophysical and structural characterization of airway submucosal gland mucus in health and diseaseP01HL164320 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Richard Charles Boucher, Michael Rubinstein · 2022 to 2026
$13.9M
Mucociliary innate defense mechanism in the human distal airwayR01HL163602 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Kenichi Okuda · 2023 to 2026
$2.4M
Pre-Clinical Evaluation of IRE1beta as a Novel Therapeutic Target for Cystic Fibrosis Airway Mucus ProductionR01HL155261 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI RIBEIRO, CARLA MARIA PEDROSA · 2021 to 2024
$1.8M
NHLBI NIH HHS P01 HL164320NHLBI NIH HHS R01 HL155261NHLBI NIH HHS R01 HL163602
6 · The paper itself

Abstract

Cystic fibrosis (CF) is caused by pathogenic variants of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene. CF in the airways is associated with dehydrated and hyperconcentrated mucus, impaired mucociliary transport, and inflammation. Although CF is a genetic disorder, CFTR sequence variations alone may not fully explain its phenotypic variation. Additionally, while pharmacological CFTR modulators that correct CFTR protein function greatly improve clinical outcomes, people with CF treated with modulators can still exhibit abnormal mucus and persistent inflammation compared to non-CF individuals. As such, understanding the regulation of mucus and inflammation remains crucial to full characterization and management of CF. We suggest that non-DNA-sequence-based mechanisms that regulate CFTR, mucus, and inflammation contribute to CF pathogenesis. This review highlights three features of transcriptional regulation known to modify gene expression (DNA methylation, histone modifications, and three-dimensional chromatin organization) and their role in CF airways. For each feature, we discuss current knowledge of their role in regulating CFTR, gel-forming mucin genes, and inflammation in CF contexts. We also highlight exploratory efforts to target epigenetic mechanisms as CF treatment strategies and suggest that epigenetics and chromatin organization offer a rich space for future CF research.

Indexed as

Chromatin organizationEpigeneticsInflammationMucus hyperconcentration

Identifiers

PMID42744679
PMCPMC13578995

What OpenQuestion holds

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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.