Evidence map›Paper›PMID 42634972›Full record

ReviewDisease models & mechanisms2026

The instructive scar - the dynamic role of extracellular matrix in biliary pathophysiology.

Scott H Waddell, Euan Brennan, Luke Boulter

Abstract readReview
In one paragraph

Review in Disease models & mechanisms, 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

3 authors.

Scott H WaddellInstitute of Genetics and Cancer, University of Edinburgh, Crewe Road South, Edinburgh EH4 2XU, UK.ORCID 0000-0002-8696-5481
Euan BrennanInstitute of Genetics and Cancer, University of Edinburgh, Crewe Road South, Edinburgh EH4 2XU, UK.ORCID 0009-0004-5311-1676
Luke BoulterInstitute of Genetics and Cancer, University of Edinburgh, Crewe Road South, Edinburgh EH4 2XU, UK.ORCID 0000-0002-7954-6705

Funding

Cancer Research UK C52499/A27948Cancer Research UK CTRQQR-2021\100006Cancer Research UK PRCBTP-May24/100001Carnegie Dunfermline Trust RIG012508Chief Scientist Office EPD/22/12Medical Research Council MR/Z506199/1
6 · The paper itself

Abstract

Cholangiopathies - congenital and acquired diseases of the hepatic bile ducts within the liver - are often considered rare pathologies but contribute to a significant proportion of all liver transplantations. Cholangiopathies present a challenge in the clinic, often due to a lack of targeted, specific therapies, thereby underscoring the need for the development of new treatments. As with many chronic diseases, cholangiopathies exist as a spectrum; they are associated with increased inflammation and fibrosis throughout disease progression that, ultimately, result in reduced liver function and increased likelihood of developing biliary tract cancers (cholangiocarcinoma). Fibrotic scarring surrounding diseased bile ducts is characterised by aberrant changes to the molecular composition of the extracellular matrix. The contribution of individual cell types to the deposition and remodelling of the extracellular matrix, as well as its molecular composition, varies between cholangiopathies. Although a broad-strokes characterisation of the extracellular matrix is well established, how it conveys biochemical and biomechanical signals to the biliary epithelial cells (cholangiocytes) and how these interactions inform ductular cells to coordinate tissue-level regeneration and underpin the molecular pathology of the cholangiopathies is not well understood. In this Review, we explore the mechanisms and roles of an altered extracellular matrix in cholangiopathies and discuss the current and future perspectives for therapeutic strategies for targeting these processes in the clinic to intervene in cholangiopathies.

Indexed as

Biliary TractCicatrixExtracellular MatrixAnimalsHumansBile ductCholangiopathiesDiseaseExtracellular matrixScar

Identifiers

PMID42634972
PMCPMC13580602

What OpenQuestion holds

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Registered trials

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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.