Evidence map›Paper›PMID 18948067›Full record

ArticleDigestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver2009

Human cholangiocarcinoma development is associated with dysregulation of opioidergic modulation of cholangiocyte growth.

M Marzioni, P Invernizzi, C Candelaresi, M Maggioni, S Saccomanno, C Selmi, C Rychlicki, L Agostinelli, B Cassani, M Miozzo and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.6field-weighted citation impact, top 39% of its field
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

11 citing papers in PubMed, 14 citations in OpenAlex.

  1. Cholangiocytes' primary cilia regulate DNA damage response and repair.American journal of physiology. Gastrointestinal and liver physiology · 2025
    Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
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  9. Autocrine regulation of biliary pathology by activated cholangiocytes.American journal of physiology. Gastrointestinal and liver physiology · 2012
    Review
  10. Molecular pathogenesis of cholangiocarcinoma.International journal of hepatology · 2012
    Article
  11. Recent advances in the regulation of cholangiocarcinoma growth.American journal of physiology. Gastrointestinal and liver physiology · 2010
    Review
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

14 authors at 5 institutions in 2 countries.

M MarzioniDepartment of Gastroenterology, Politechnic University of Marche, Ancona, Italy. m.marzioni@univpm.it
P Invernizzi
C Candelaresi
M Maggioni
S Saccomanno
C Selmi
C Rychlicki
L Agostinelli
B Cassani
M Miozzo
S Pasini
G Fava
G Alpini
A Benedetti
Marche Polytechnic University · ITOspedale San Paolo · ITUniversity of California, Davis · USUniversity of Milan · ITCentral Texas Veterans Health Care System · US

Funding

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
NIDDK NIH HHS R01 DK062975
6 · The paper itself

Abstract

BACKGROUND/

aimsIncidence of cholangiocarcinoma is increasing worldwide, yet remaining highly aggressive and with poor prognosis. The mechanisms that drive cholangiocyte transition towards malignant phenotype are obscure. Cholangiocyte benign proliferation is subjected to a self-limiting mechanism based on the autocrine release of endogenous opioid peptides. Despite the presence of both, ligands interact with delta opioid receptor (OR), but not with microOR, with the consequent inhibition of cell growth. We aimed to verify whether cholangiocarcinoma growth is associated with failure of opioidergic regulation of growth control.

methodsWe evaluated the effects of OR selective agonists on cholangiocarcinoma cell proliferation, migration and apoptosis. Intracellular signals were also characterised.

resultsActivation of microOR, but not deltaOR, increases cholangiocarcinoma cell growth. Such an effect is mediated by ERK1/2, PI3K and Ca(2+)-CamKIIalpha cascades, but not by cAMP/PKA and PKCalpha. microOR activation also enhances cholangiocarcinoma cell migration and reduces death by apoptosis. The anti-apoptotic effect of microOR was PI3K dependent.

conclusionsOur data indicate that cholangiocarcinoma growth is associated with altered opioidergic regulation of cholangiocyte biology, thus opening new scenarios for future surveillance or early diagnostic strategies for cholangiocarcinoma.

Indexed as

Cell ProliferationApoptosisCell Line, TumorCell MovementCholangiocarcinomaHumansReceptors, Opioid, deltaReceptors, Opioid, muSignal TransductionReceptors, Opioid, deltaReceptors, Opioid, mu

Identifiers

PMID18948067
PMCPMC2692367
OpenAlexW2102707555

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.