Evidence map›Paper›PMID 29095436›Full record

ArticleCell death & disease2017

RNA-sequencing-based comparative analysis of human hepatic progenitor cells and their niche from alcoholic steatohepatitis livers.

An Ceulemans, Stefaan Verhulst, Matthias Van Haele, Olivier Govaere, Juan-Jose Ventura, Leo A van Grunsven, Tania Roskams

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 18% 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, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. IL-1 family of cytokines in gastrointestinal and liver disorders.Nature reviews. Gastroenterology & hepatology · 2026
    Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Complement C1q mediates the expansion of periportal hepatic progenitor cells in senescence-associated inflammatory liver.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  9. Article
  10. Review
  11. 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

7 authors at 2 institutions in 2 countries.

An CeulemansDepartment of Imaging and Pathology, Translational Cell and Tissue Research, KU Leuven and University Hospitals, Leuven, Belgium.
Stefaan VerhulstLiver Cell Biology Lab, Department of Basic Biomedical Sciences, Vrije Universiteit Brussel, Brussels, Belgium.
Matthias Van HaeleDepartment of Imaging and Pathology, Translational Cell and Tissue Research, KU Leuven and University Hospitals, Leuven, Belgium.
Olivier GovaereLaboratory for Translational Cell and Tissue Research, Department of Imaging and Pathology, KU Leuven - University of Leuven, Leuven, Belgium.
Juan-Jose VenturaDepartment of Imaging and Pathology, Translational Cell and Tissue Research, KU Leuven and University Hospitals, Leuven, Belgium.
Leo A van GrunsvenLiver Cell Biology Lab, Department of Basic Biomedical Sciences, Vrije Universiteit Brussel, Brussels, Belgium.
Tania RoskamsDepartment of Imaging and Pathology, Translational Cell and Tissue Research, KU Leuven and University Hospitals, Leuven, Belgium.
KU Leuven · BEVrije Universiteit Brussel · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatic progenitor cells (HPCs) are small cells with a relative large oval nucleus and a scanty cytoplasm situated in the canals of Hering that express markers of (immature) hepatocytes and cholangiocytes. HPCs are present in large numbers in alcoholic steatohepatitis (ASH), one of the leading causes of chronic liver disease. To date, the mechanisms responsible for proliferation and differentiation of human HPCs are still poorly understood and the role of HPCs in ASH development is unknown. In this study, we aimed to characterise human HPCs and their interactions with other cells through comparison, on both protein and RNA level, of HPC-enriched cell populations from adult human liver tissue using different isolation methods. Fresh human liver tissue was collected from ASH explant livers and HPC-enriched cell populations were obtained via four different isolation methods: side population (SP), epithelial cell adhesion molecule (EpCAM) and trophoblast antigen 2 (TROP-2) membrane marker isolation and laser capture microdissection. Gene expression profiles of fluorescent-activated cell-sorted HPCs, whole liver extracts and laser microdissected HPC niches were determined by RNA-sequencing. Immunohistochemical evaluation of the isolated populations indicated the enrichment of HPCs in the SP, EpCAM

Indexed as

Antigens, NeoplasmAutocrine CommunicationCell Adhesion MoleculesCell Culture TechniquesCluster AnalysisCytokine TWEAKEpithelial Cell Adhesion MoleculeFatty Liver, AlcoholicHepatocyte Growth FactorHumansImmunohistochemistryInsulin-Like Growth Factor IInterleukin-17LiverMacrophage Migration-Inhibitory FactorsMicroscopy, FluorescenceAntigens, NeoplasmCell Adhesion MoleculesCytokine TWEAKEpithelial Cell Adhesion MoleculeHepatocyte Growth FactorInsulin-Like Growth Factor IInterleukin-17Macrophage Migration-Inhibitory FactorsRNATACSTD2 protein, humanTNFSF12 protein, human

Identifiers

PMID29095436
PMCPMC5775409
OpenAlexW2766680276

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.