Evidence map›Paper›PMID 29248454›Full record

ArticleThe American journal of pathology2018

Acquisition of Cholangiocarcinoma Traits during Advanced Hepatocellular Carcinoma Development in Mice.

Liyuan Li, Maoxiang Qian, I-Hsuan Chen, David Finkelstein, Arzu Onar-Thomas, Melissa Johnson, Christopher Calabrese, Armita Bahrami, Dolores H López-Terrada, Jun J Yang and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

20 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
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  6. Organoids and spheroids: advancedFrontiers in cell and developmental biology · 2024
    Review
  7. Article
  8. Article
  9. Article
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  12. Review
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  14. KIF2C promotes the proliferation of hepatocellular carcinoma cellsExperimental and therapeutic medicine · 2021
    Article
  15. Article
  16. Review
  17. Review
  18. Organoids for the Study of Liver Cancer.Seminars in liver disease · 2021
    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

12 authors at 3 institutions in 1 country.

Liyuan LiDepartment of Pharmaceutical Sciences, St. Jude Children's Research Hospital, Memphis, Tennessee.
Maoxiang QianDepartment of Pharmaceutical Sciences, St. Jude Children's Research Hospital, Memphis, Tennessee.
I-Hsuan ChenDepartment of Biochemistry, Purdue University, West Lafayette, Indiana.
David FinkelsteinDepartment of Computational Biology, St. Jude Children's Research Hospital, Memphis, Tennessee.
Arzu Onar-ThomasDepartment of Statistics, St. Jude Children's Research Hospital, Memphis, Tennessee.
Melissa JohnsonDepartment of Small Animal Imaging Core, St. Jude Children's Research Hospital, Memphis, Tennessee.
Christopher CalabreseDepartment of Small Animal Imaging Core, St. Jude Children's Research Hospital, Memphis, Tennessee.
Armita BahramiDepartment of Pathology, St. Jude Children's Research Hospital, Memphis, Tennessee.
Dolores H López-TerradaDepartment of Pathology, Texas Children's Hospital and Baylor College of Medicine, Houston, Texas.
Jun J YangDepartment of Pharmaceutical Sciences, St. Jude Children's Research Hospital, Memphis, Tennessee.
W Andy TaoDepartment of Biochemistry, Purdue University, West Lafayette, Indiana.
Liqin ZhuDepartment of Pharmaceutical Sciences, St. Jude Children's Research Hospital, Memphis, Tennessee. Electronic address: liqin.zhu@stjude.org.
St. Jude Children's Research Hospital · USPurdue University West Lafayette · USBaylor College of Medicine · US

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
New Proteomic Technologies for the Analysis of Tyrosine Kinase Signaling PathwaysR01GM088317 · NIGMS · PURDUE UNIVERSITY · PI TAO, W. ANDY · 2010 to 2014
$1.6M
A Proteomic Platform to identify and Validate Biomarkers in Metabolic Syndrome and Coronary Artery DiseaseR01GM111788 · NIGMS · PURDUE UNIVERSITY · PI TAO, W. ANDY · 2015 to 2017
$900k
NCI NIH HHS P30 CA021765NIGMS NIH HHS R01 GM088317NIGMS NIH HHS R01 GM111788
6 · The paper itself

Abstract

Past studies have identified hepatic tumors with mixed hepatocellular carcinoma (HCC) and cholangiocarcinoma (CC) characteristics that have a more aggressive behavior and a poorer prognosis than classic HCC. Whether this pathologic heterogeneity is due to a cell of origin of bipotent liver progenitors or the plasticity of cellular constituents comprising these tumors remains debated. In this study, we investigated the potential acquisition of CC-like traits during advanced development of HCC in mice. Primary and rare high-grade HCC developed in a genetic mouse model. A mouse model of highly efficient HCC invasion and metastasis by orthotopic transplantation of liver cancer organoids propagated from primary tumors in the genetic model was further developed. Invasive/metastatic tumors developed in both models closely recapitulated advanced human HCC and displayed a striking acquisition of CC-related pathologic and molecular features, which was absent in the primary HCC tumors. Our study directly demonstrates the pathologic evolution of HCC during advanced tumor development, providing the first evidence that tumors with mixed HCC and CC features, or at least a subset of these tumors, represent a more advanced developmental stage of HCC. Finally, liver cancer organoid-generated high-grade tumors exhibited significantly increased extracellular vesicle secretion, suggesting that identifying tumor-specific extracellular vesicle proteins in plasma may be a promising tool for liver cancer detection.

Indexed as

AnimalsCarcinoma, HepatocellularCholangiocarcinomaDisease Models, AnimalGene Expression Regulation, NeoplasticLiverLiver NeoplasmsMiceMice, KnockoutNeoplasm InvasivenessPrognosisTumor Burden

Identifiers

PMID29248454
PMCPMC5840495
OpenAlexW2774608833

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.