Evidence map›Paper›PMID 26273695›Full record

ArticleCellular and molecular gastroenterology and hepatology2015

Functional and structural features of cholangiocytes in health and disease.

Luca Maroni, Bai Haibo, Debolina Ray, Tianhao Zhou, Ying Wan, Fanyin Meng, Marco Marzioni, Gianfranco Alpini

Abstract read
In one paragraph

Article in Cellular and molecular gastroenterology and hepatology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing 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

69 citing papers in PubMed.

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9 more citing papers are in PubMed but not listed here.

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

8 authors.

Luca MaroniDepartment of Gastroenterology and Hepatology, Università Politecnica delle Marche, Ancona, Italy.
Bai HaiboScott & White Digestive Disease Research Center, Scott & White, Texas A&M University Health Science Center, Temple, TX 76504.
Debolina RayDepartment of Medicine, Division Gastroenterology, Texas A&M University Health Science Center, Temple, TX 76504.
Tianhao ZhouDepartment of Medicine, Division Gastroenterology, Texas A&M University Health Science Center, Temple, TX 76504.
Ying WanScott & White Digestive Disease Research Center, Scott & White, Texas A&M University Health Science Center, Temple, TX 76504.
Fanyin MengResearch, Central Texas Veterans Health Care System, Texas A&M University Health Science Center, Temple, TX 76504 ; Scott & White Digestive Disease Research Center, Scott & White, Texas A&M University Health Science Center, Temple, TX 76504 ; Department of Medicine, Division Gastroenterology, Texas A&M University Health Science Center, Temple, TX 76504.
Marco MarzioniDepartment of Gastroenterology and Hepatology, Università Politecnica delle Marche, Ancona, Italy.
Gianfranco AlpiniResearch, Central Texas Veterans Health Care System, Texas A&M University Health Science Center, Temple, TX 76504 ; Scott & White Digestive Disease Research Center, Scott & White, Texas A&M University Health Science Center, Temple, TX 76504 ; Department of Medicine, Division Gastroenterology, Texas A&M University Health Science Center, Temple, TX 76504.

Funding

GROWTH REGULATION OF THE INTRAHEPATIC BILIARY TREER01DK054811 · NIDDK · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI ALPINI, GIANFRANCO D, GLASER, SHANNON STROUD · 2000 to 2021
$3.8M
Role of Sensory Neuropeptides in the Regulation of Biliary FunctionR01DK076898 · NIDDK · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI ALPINI, GIANFRANCO D, GLASER, SHANNON STROUD · 2008 to 2016
$1.8M
The Role of Stem Cell Derived Microvesicles in Cholestatic Liver InjuryR01DK107310 · NIDDK · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI ALPINI, GIANFRANCO D, GLASER, SHANNON STROUD · 2015 to 2019
$1.7M
Autocrine/Paracrine Regulation of Intrahepatic Bile Duct GrowthI01BX000574 · VA · RLR VA MEDICAL CENTER · PI ALPINI, GIANFRANCO D · 2009 to 2022
–
Functional characters of non-coding RNAs in alcoholic liver injuryI01BX001724 · VA · RLR VA MEDICAL CENTER · PI MENG, FANYIN · 2012 to 2024
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BLRD VA I01 BX000574BLRD VA I01 BX001724NIDDK NIH HHS R01 DK054811NIDDK NIH HHS R01 DK076898NIDDK NIH HHS R01 DK107310
6 · The paper itself

Abstract

Cholangiocytes are the epithelial cells that line the bile ducts. Along the biliary tree, two different kinds of cholangiocytes exist; small and large cholangiocytes. Each type has important differences in their biological role in physiological and pathological conditions. In response to injury, cholangiocytes become reactive and acquire a neuroendocrine-like phenotype with the secretion of a number of peptides. These molecules act in an autocrine/paracrine fashion to modulate cholangiocyte biology and determine the evolution of biliary damage. The failure of such mechanisms is believed to influence the progression of cholangiopathies, a group of diseases that selectively target biliary cells. Therefore, the understanding of mechanisms regulating cholangiocyte response to injury is expected to foster the development of new therapeutic options to treat biliary diseases. In the present review, we will discuss the most recent findings in the mechanisms driving cholangiocyte adaptation to damage, with particular emphasis on molecular pathways that are susceptible of therapeutic intervention. Morphogenic pathways (Hippo, Notch, Hedgehog), which have been recently shown to regulate biliary ontogenesis and response to injury, will also be reviewed. In addition, the results of ongoing clinical trials evaluating new drugs for the treatment of cholangiopathies will be discussed.

Indexed as

Biliary EpitheliumPrimary Biliary CirrhosisPrimary Sclerosing Cholangitis

Identifiers

PMID26273695
PMCPMC4530547

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.