Evidence map›Paper›PMID 35326593›Full record

ReviewCancers2022

Molecular Mechanisms Linking Risk Factors to Cholangiocarcinoma Development.

Ludovica Ceci, Tianhao Zhou, Ilaria Lenci, Vik Meadows, Lindsey Kennedy, Ping Li, Burcin Ekser, Martina Milana, Wenjun Zhang, Chaodong Wu and 6 more

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
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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 4 institutions in 2 countries.

Ludovica CeciHepatology and Gastroenterology Division, Department of Medicine, Indiana University, Indianapolis, IN 46202, USA.
Tianhao ZhouHepatology and Gastroenterology Division, Department of Medicine, Indiana University, Indianapolis, IN 46202, USA.
Ilaria LenciUnit of Hepatology, Tor Vergata University, 00133 Rome, Italy.
Vik MeadowsHepatology and Gastroenterology Division, Department of Medicine, Indiana University, Indianapolis, IN 46202, USA.ORCID 0000-0002-8983-4305
Lindsey KennedyHepatology and Gastroenterology Division, Department of Medicine, Indiana University, Indianapolis, IN 46202, USA.
Ping LiDepartment of Surgery, Division of Transplant Surgery, Indiana University, Indianapolis, IN 46202, USA.
Burcin EkserDepartment of Surgery, Division of Transplant Surgery, Indiana University, Indianapolis, IN 46202, USA.ORCID 0000-0003-0741-8007
Martina MilanaUnit of Hepatology, Tor Vergata University, 00133 Rome, Italy.
Wenjun ZhangDepartment of Surgery, Division of Transplant Surgery, Indiana University, Indianapolis, IN 46202, USA.ORCID 0000-0001-9801-0634
Chaodong WuDepartment of Nutrition, Texas A&M University, College Station, TX 77843, USA.
Keisaku SatoHepatology and Gastroenterology Division, Department of Medicine, Indiana University, Indianapolis, IN 46202, USA.ORCID 0000-0001-5380-8001
Sanjukta ChakrabortyDepartment of Medical Physiology, Texas A&M University College of Medicine, Bryan, TX 77807, USA.ORCID 0000-0002-4869-3198
Shannon S GlaserDepartment of Medical Physiology, Texas A&M University College of Medicine, Bryan, TX 77807, USA.
Heather FrancisHepatology and Gastroenterology Division, Department of Medicine, Indiana University, Indianapolis, IN 46202, USA.
Gianfranco AlpiniHepatology and Gastroenterology Division, Department of Medicine, Indiana University, Indianapolis, IN 46202, USA.ORCID 0000-0002-6658-3021
Leonardo BaiocchiUnit of Hepatology, Tor Vergata University, 00133 Rome, Italy.
Indiana University – Purdue University Indianapolis · USRichard L. Roudebush VA Medical Center · USTexas A&M University · USUniversity of Rome Tor Vergata · 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
The Paracrine Regulation of Mast Cells During Biliary/Cholangiocyte Repair and DamageR01DK108959 · NIDDK · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI FRANCIS, HEATHER L · 2016 to 2024
$2.5M
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
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
Mechanisms of mast cell/cholangiocyte regulation of non-alcoholic fatty liver disease progressionR01DK119421 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI FRANCIS, HEATHER L · 2019 to 2022
$1.4M
Neuroendocrine Regulation of Biliary Growth and FibrosisR01DK110035 · NIDDK · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI ALPINI, GIANFRANCO D, GLASER, SHANNON STROUD · 2017 to 2020
$1.2M
Regulation of biliary growth and fibrosis by melatoninR01DK115184 · NIDDK · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI ALPINI, GIANFRANCO D, GLASER, SHANNON STROUD · 2017 to 2020
$1.2M
REGULATION OF CELLULAR SENESCENCE BY NON-CODING RNAS IN ALCOHOLIC LIVER INJURYR21AA025997 · NIAAA · SCOTT AND WHITE MEMORIAL HOSPITAL · PI ALPINI, GIANFRANCO D, MENG, FANYIN · 2017 to 2018
$435k
Role of stem cell derived microvesicles in alcoholic liver injuryR21AA025157 · NIAAA · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI ALPINI, GIANFRANCO D, MENG, FANYIN · 2017 to 2018
$350k
BLR&D Research Career Scientist AwardIK6BX005226 · VA · RLR VA MEDICAL CENTER · PI FRANCIS, HEATHER L · 2020 to 2024
–
Cholangiocyte-Derived Endothelin Signaling Mediates Biliary Injury and Liver FibrosisIK2BX005306 · VA · RLR VA MEDICAL CENTER · PI KENNEDY, LINDSEY · 2021 to 2024
–
BLRD VA I01 BX000574BLRD VA I01 BX003031BLRD VA IK2 BX005306BLRD VA IK6 BX004601BLRD VA IK6 BX005226NIH HHS AA025157NIH HHS AA025997NIH HHS DK054811NIH HHS DK062975NIH HHS DK076898NIH HHS DK107310NIH HHS DK108959NIH HHS DK110035NIH HHS DK115184NIH HHS DK119421
6 · The paper itself

Abstract

The poor prognosis of cholangiocarcinoma in humans is related to several factors, such as (i) the heterogeneity of the disease, (ii) the late onset of symptoms and (iii) the limited comprehension of the carcinogenic pathways determining neoplastic changes, which all limit the pursuit of appropriate treatment. Several risk factors have been recognized, including different infective, immune-mediated, and dysmorphogenic disorders of the biliary tree. In this review, we report the details of possible mechanisms that lead a specific premalignant pathological condition to become cholangiocarcinoma. For instance, during liver fluke infection, factors secreted from the worms may play a major role in pathogenesis. In primary sclerosing cholangitis, deregulation of histamine and bile-acid signaling may determine important changes in cellular pathways. The study of these molecular events may also shed some light on the pathogenesis of sporadic (unrelated to risk factors) forms of cholangiocarcinoma, which represent the majority (nearly 75%) of cases.

Indexed as

bile duct cystscholangiocarcinomacirrhosisliver flukeprimary sclerosing cholangitisrisk factor

Identifiers

PMID35326593
PMCPMC8945938
OpenAlexW4220988020

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.