Evidence map›Paper›PMID 19291182›Full record

ArticleLiver international : official journal of the International Association for the Study of the Liver2009

Endothelin inhibits cholangiocarcinoma growth by a decrease in the vascular endothelial growth factor expression.

Giammarco Fava, Sharon Demorrow, Eugenio Gaudio, Antonio Franchitto, Paolo Onori, Guido Carpino, Shannon Glaser, Heather Francis, Monique Coufal, Luca Marucci and 6 more

Open access · greenAbstract read
In one paragraph

Article in Liver international : official journal of the International 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 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

22 citing papers in PubMed, 38 citations in OpenAlex.

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  14. Liver carcinogenesis: rodent models of hepatocarcinoma and cholangiocarcinoma.Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver · 2013
    Review
  15. Article
  16. Review
  17. Autocrine regulation of biliary pathology by activated cholangiocytes.American journal of physiology. Gastrointestinal and liver physiology · 2012
    Review
  18. Article
  19. Molecular pathogenesis of cholangiocarcinoma.International journal of hepatology · 2012
    Article
  20. 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

16 authors at 6 institutions in 2 countries.

Giammarco FavaDepartment of Gastroenterology, Universita' Politecnica delle Marche, Ancona, Italy.
Sharon Demorrow
Eugenio Gaudio
Antonio Franchitto
Paolo Onori
Guido Carpino
Shannon Glaser
Heather Francis
Monique Coufal
Luca Marucci
Domenico Alvaro
Marco Marzioni
Trenton Horst
Romina Mancinelli
Antonio Benedetti
Gianfranco Alpini
Marche Polytechnic University · ITSapienza University of Rome · ITTexas A&M Health Science Center · USBaylor Scott & White Medical Center - Temple · USCentral Texas Veterans Health Care System · USUniversity of L'Aquila · IT

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
Endocannabinoid Regulation of Cholangiocarcinoma Cell GrowthK01DK078532 · NIDDK · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI DEMORROW, SHARON · 2007 to 2011
$697k
NIDDK NIH HHS DK062975NIDDK NIH HHS DK58411NIDDK NIH HHS DK76898NIDDK NIH HHS K01 DK078532NIDDK NIH HHS KO1DK078532NIDDK NIH HHS R01 DK054811NIDDK NIH HHS R01 DK058411NIDDK NIH HHS R01 DK062975NIDDK NIH HHS R01 DK076898
6 · The paper itself

Abstract

backgroundEndothelins (ET-1, ET-2, ET-3) are peptides with vasoactive properties interacting with ET(A) and ET(B) receptors. ET-1 inhibits secretin-stimulated ductal secretion (hallmark of cholangiocyte growth) of cholestatic rats by interaction with ET receptors.

aimThe aims of the studies were to evaluate (i) the effect of ET-1 on cholangiocarcinoma growth in Mz-ChA-1 cells and nude mice and (ii) whether ET-1 regulation of cholangiocarcinoma growth is associated with changes in the expression of vascular endothelial growth factor-A (VEGF-A), VEGF-C, VEGF receptor-2 (VEGFR-2) and VEGFR-3.

methodsWe determined the expression of ET(A) and ET(B) receptors on normal and malignant (Mz-ChA-1) cholangiocytes and human cholangiocarcinoma tissue and the effect of ET-1 on the proliferation and expression of VEGF-A, VEGF-C (regulators of tumour angiogenesis) and its receptors, VEGFR-2 and VEGFR-3, in Mz-ChA-1 cells. In vivo, Mz-ChA-1 cells were injected into the flanks of athymic mice and injections of ET-1 or saline into the tumours were performed daily. The effect of ET-1 on tumour size, cell proliferation, apoptosis, collagen quantity and the expression of VEGF-A and VEGF-C and VEGFR-2 and VEGFR-3 were measured after 73 days.

resultsHigher expression of ET(A) and ET(B) was observed in malignant compared with normal cholangiocytes. ET-1 inhibited proliferation and VEGF-A, VEGF-C, VEGFR-2 and VEGFR-3 expression of Mz-ChA-1 cells. Chronic ET-1 treatment decreased tumour volume, tumour cell proliferation and VEGF-A and VEGF-C expression but increased apoptosis and collagen tissue deposition compared with controls.

conclusionsModulation of VEGF-A and VEGF-C (by ET-1) may be important for managing cholangiocarcinoma growth.

Indexed as

Cell ProliferationAnimalsApoptosisBile Duct NeoplasmsBile Ducts, IntrahepaticCell Line, TumorCholangiocarcinomaCollagenDown-RegulationEndothelin-1Gene Expression Regulation, NeoplasticHumansMaleMiceMice, Inbred BALB CMice, NudeCollagenEndothelin-1Receptor, Endothelin AReceptor, Endothelin BRNA, MessengerVascular Endothelial Growth Factor AVascular Endothelial Growth Factor CVascular Endothelial Growth Factor Receptor-2Vascular Endothelial Growth Factor Receptor-3VEGFA protein, human

Identifiers

PMID19291182
PMCPMC2706939
OpenAlexW2016331309

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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.