Evidence map›Paper›PMID 42918857›Full record

ReviewNature reviews. Rheumatology2026

Primary cilia as regulators of fibrosis and potential therapeutic targets.

Maria E Teves, John Varga

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Rheumatology, 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

2 authors.

Maria E TevesDepartment of Obstetrics & Gynecology, Virginia Commonwealth University, Richmond, VA, USA. maria.teves@vcuhealth.org.
John VargaDivision of Rheumatology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI, USA. vargaj@umich.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fibrosis complicates numerous rheumatic diseases and accounts for considerable morbidity and mortality. Developing more effective treatments will require a deeper understanding of fibrosis. Discoveries over the past decade implicate the ubiquitous cellular organelle primary cilium in modulating tissue repair in health and disease. In particular, emerging evidence shows that dysregulated function of primary cilia might have a previously unrecognized pathogenic role in fibrosis across multiple organs and conditions. Historically considered vestigial organelles, primary cilia are complex microtubule-based solitary organelles present on most vertebrate cells. They function as signalling hubs for Toll-like receptors and receptors for morphogen and growth factors and thereby regulate physiological and pathological tissue remodelling. Pharmacological modulation of primary cilia represents a potential approach to target cellular function and could offer a future therapeutic strategy for fibrotic diseases.

Identifiers

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.