Evidence map›Paper›PMID 26597881›Full record

ArticleThe American journal of pathology2016

Inhibition of Mast Cell-Derived Histamine Decreases Human Cholangiocarcinoma Growth and Differentiation via c-Kit/Stem Cell Factor-Dependent Signaling.

Christopher Johnson, Victoria Huynh, Laura Hargrove, Lindsey Kennedy, Allyson Graf-Eaton, Jennifer Owens, Jerome P Trzeciakowski, Kyle Hodges, Sharon DeMorrow, Yuyan Han and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

47 citing papers in PubMed, 69 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Article
  6. Pro-Tumorigenic Effect of Continuous Cromolyn Treatment in Bladder Cancer.International journal of molecular sciences · 2025
    Article
  7. Review
  8. Review
  9. Pathophysiological role of histamine signaling and its implications in glioblastoma.Biochimica et biophysica acta. Reviews on cancer · 2024
    Review
  10. Review
  11. Review
  12. Lymphatic vasculature in ovarian cancer.Biochimica et biophysica acta. Reviews on cancer · 2023
    Review
  13. Review
  14. Article
  15. Article
  16. The Functional Roles of Immune Cells in Primary Liver Cancer.The American journal of pathology · 2022
    Review
  17. Review
  18. Review
  19. Review
  20. 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

13 authors at 3 institutions in 1 country.

Christopher JohnsonScott & White Digestive Disease Research Center, Temple, Texas.
Victoria HuynhScott & White Digestive Disease Research Center, Temple, Texas.
Laura HargroveScott & White Digestive Disease Research Center, Temple, Texas.
Lindsey KennedyDepartment of Research, Central Texas Veterans Health Care System, Temple, Texas.
Allyson Graf-EatonDepartment of Research, Central Texas Veterans Health Care System, Temple, Texas.
Jennifer OwensDepartment of Research, Central Texas Veterans Health Care System, Temple, Texas.
Jerome P TrzeciakowskiDepartment of Medical Physiology, Texas A&M Health Science Center, Temple, Texas.
Kyle HodgesScott & White Digestive Disease Research Center, Temple, Texas.
Sharon DeMorrowScott & White Digestive Disease Research Center, Temple, Texas; Department of Research, Central Texas Veterans Health Care System, Temple, Texas; Department of Medicine, Scott & White Healthcare, Temple, Texas.
Yuyan HanScott & White Digestive Disease Research Center, Temple, Texas; Department of Medicine, Scott & White Healthcare, Temple, Texas.
Lucas WongScott & White Digestive Disease Research Center, Temple, Texas; Department of Medicine, Scott & White Healthcare, Temple, Texas.
Gianfranco AlpiniScott & White Digestive Disease Research Center, Temple, Texas; Department of Research, Central Texas Veterans Health Care System, Temple, Texas; Department of Medical Physiology, Texas A&M Health Science Center, Temple, Texas; Department of Medicine, Scott & White Healthcare, Temple, Texas.
Heather FrancisScott & White Digestive Disease Research Center, Temple, Texas; Department of Research, Central Texas Veterans Health Care System, Temple, Texas; Department of Medicine, Scott & White Healthcare, Temple, Texas. Electronic address: hfrancis@medicine.tamhsc.edu.
Baylor Scott & White Medical Center - Temple · USCentral Texas Veterans Health Care System · USTexas A&M Health Science Center · US

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
Dysregulation of hypothalamic neuropeptides is associated with biliary hyperplasiaR01DK082435 · NIDDK · UNIVERSITY OF TEXAS AT AUSTIN · PI DEMORROW, SHARON · 2010 to 2020
$2.7M
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
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
–
Mechanisms of synergistic regulation of biliary inflammation and fibrosisI01BX003031 · VA · RLR VA MEDICAL CENTER · PI FRANCIS, HEATHER L · 2016 to 2023
–
The role of hypothalamic neuropeptides on biliary function during cholestasisI01BX002638 · VA · OLIN TEAGUE VETERANS CENTER · PI DEMORROW, SHARON · 2015 to 2018
–
BLRD VA I01 BX000574BLRD VA I01 BX002638BLRD VA I01 BX003031NIDDK NIH HHS R01 DK054811NIDDK NIH HHS R01 DK076898NIDDK NIH HHS R01 DK082435NIDDK NIH HHS R01 DK107310NIDDK NIH HHS R01 DK108959
6 · The paper itself

Abstract

The tumor microenvironment of cholangiocarcinoma (CCA) is composed of numerous cells, including mast cells (MCs). MCs release histamine, which increases CCA progression and angiogenesis. Cholangiocytes secrete stem cell factor, which functions via the MC growth factor receptor c-Kit. Here, we show that cholangiocytes express histidine decarboxylase and its inhibition reduces CCA growth. MC recruitment in the tumor microenvironment increased CCA growth. MC infiltration and MC markers were detected by toluidine blue staining and real-time PCR in human biopsies and in tumors from athymic mice treated with saline, histamine, histidine decarboxylase inhibitor, or cromolyn sodium. Tumor growth, angiogenesis, and epithelial-mesenchymal transition (EMT)/extracellular matrix (ECM) markers were measured in mice treated with cromolyn sodium. In vitro, human CCA cells were treated with MC supernatant fluids before evaluating angiogenesis and EMT/ECM expression. Migration assays were performed with CCA cells treated with the stem cell factor inhibitor. MC supernatant fluids increased CCA histidine decarboxylase, vascular endothelial growth factor, and MC/EMT/ECM expression that decreased with pretreatment of cromolyn sodium. MCs were found in human biopsies. In mice treated with cromolyn sodium, MC infiltration and tumor growth decreased. Inhibition of CCA stem cell factor blocked MC migration and MC/EMT/ECM in CCA. MCs migrate into CCA tumor microenvironment via c-Kit/stem cell factor and increase tumor progression, angiogenesis, EMT switch, and ECM degradation.

Indexed as

AnimalsBile Duct NeoplasmsCell DifferentiationCell ProliferationCholangiocarcinomaEpithelial-Mesenchymal TransitionFluorescent Antibody TechniqueHeterograftsHistamineHumansImmunohistochemistryMast CellsMiceMice, NudeNeovascularization, PathologicProto-Oncogene Proteins c-kitHistamineProto-Oncogene Proteins c-kitStem Cell Factor

Identifiers

PMID26597881
PMCPMC5707204
OpenAlexW2172664276

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.