Evidence map›Paper›PMID 22194419›Full record

ReviewAmerican journal of physiology. Gastrointestinal and liver physiology2012

Autocrine regulation of biliary pathology by activated cholangiocytes.

Kendal Jensen, Marco Marzioni, Kamruzzaman Munshi, Syeda Afroze, Gianfranco Alpini, Shannon Glaser

Abstract readReview
In one paragraph

Review in American journal of physiology. Gastrointestinal and liver physiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Functional and structural features of cholangiocytes in health and disease.Cellular and molecular gastroenterology and hepatology · 2015
    Article
  8. Article
  9. General mechanisms of nicotine-induced fibrogenesis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2012
    Review
  10. 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.

Kendal JensenScott & White Digestive Disease Research Center, TX, USA.
Marco Marzioni
Kamruzzaman Munshi
Syeda Afroze
Gianfranco Alpini
Shannon Glaser

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
Regulation of Bile Duct Growth in Bile Duct Ligated RatsR01DK062975 · NIDDK · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI ALPINI, GIANFRANCO D, GLASER, SHANNON STROUD · 2005 to 2014
$1.9M
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
TOWARD THE OPTIMAL TIMING OF INITIATION OF DIALYSISR01DK058411 · NIDDK · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI CHERTOW, GLENN MATTHEW · 2001 to 2003
$1.8M
Role of the Renin-Angiotensin System in the Regulation of Biliary ProliferationR01DK081442 · NIDDK · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI GLASER, SHANNON STROUD · 2009 to 2010
$628k
NIDDK NIH HHS DK054811NIDDK NIH HHS DK58411NIDDK NIH HHS DK76898NIDDK NIH HHS R01 DK054811NIDDK NIH HHS R01 DK058411NIDDK NIH HHS R01 DK062975NIDDK NIH HHS R01 DK076898NIDDK NIH HHS R01 DK-081442NIDDK NIH HHS R01 DK081442
6 · The paper itself

Abstract

The bile duct system of the liver is lined by epithelial cells (i.e., cholangiocytes) that respond to a large number of neuroendocrine factors through alterations in their proliferative activities and the subsequent modification of the microenvironment. As such, activation of biliary proliferation compensates for the loss of cholangiocytes due to apoptosis and slows the progression of toxic injury and cholestasis. Over the course of the last three decades, much progress has been made in identifying the factors that trigger the biliary epithelium to remodel and grow. Because a large number of autocrine factors have recently been identified as relevant clinical targets, a compiled review of their contributions and function in cholestatic liver diseases would be beneficial. In this context, it is important to define the specific processes triggered by autocrine factors that promote cholangiocytes to proliferate, activate neighboring cells, and ultimately lead to extracellular matrix deposition. In this review, we discuss the role of each of the known autocrine factors with particular emphasis on proliferation and fibrogenesis. Because many of these molecules interact with one another throughout the progression of liver fibrosis, a model speculating their involvement in the progression of cholestatic liver disease is also presented.

Indexed as

AnimalsAutocrine CommunicationBile DuctsBiliary TractCell ProliferationEndothelinsEpithelial CellsEstrogensHumansIntegrinsLiver CirrhosisNeuropeptidesPeptide HormonesPlatelet-Derived Growth FactorRenin-Angiotensin SystemTransforming Growth Factor betaEndothelinsEstrogensIntegrinsNeuropeptidesPeptide HormonesPlatelet-Derived Growth Factorplatelet-derived growth factor ATransforming Growth Factor beta

Identifiers

PMID22194419
PMCPMC3774492

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.