Evidence map›Paper›PMID 24293012›Full record

ArticleMolecules and cells2013

Isolation of EpCAM(+)/CD133 (-) hepatic progenitor cells.

Pei-Pei Hao, Mi-Jin Lee, Goung-Ran Yu, In-Hee Kim, Yong-Gon Cho, Dae-Ghon Kim

Open access · bronzeAbstract read
In one paragraph

Article in Molecules and cells, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

14 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Functional characterization of CD49fJournal of molecular histology · 2022
    Article
  6. Article
  7. Article
  8. Article
  9. Shedding light on the EpCAM: An overview.Journal of cellular physiology · 2019
    Review
  10. Article
  11. Article
  12. Article
  13. Role of liver progenitors in liver regeneration.Hepatobiliary surgery and nutrition · 2015
    Review
  14. 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

6 authors at 1 institution in 1 country.

Pei-Pei HaoDivision of Gastroenterology and Hepatology, Departments of Internal Medicine, Chonbuk National University Medical School and Hospital, Jeonju, 561-712, Korea.
Mi-Jin Lee
Goung-Ran Yu
In-Hee Kim
Yong-Gon Cho
Dae-Ghon Kim
Jeonbuk National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Progenitor cell-derived hepatocytes are critical for hepatocyte replenishment. Therefore, we established a line of human hepatic progenitor (HNK1) cells and determined their biological characteristics for experimental and therapeutic applications. HNK1 cells, isolated from human noncirrhotic liver samples with septal fibrosis, showed high expression of the hepatic progenitor cell (HPC) markers EpCAM, CK7, CK19, alpha-fetoprotein (AFP), CD90 (Thy1), and EFNA1. Expression of CD133 was very low. Ductular reactions at the periphery of cirrhotic nodules were immunohistochemically positive for these HPC markers, including EFNA1. Sodium butyrate, a differentiation inducer, induced hepatocyte-like morphological changes in HNK1 cells. It resulted in down-regulation of the hepatic progenitor cell markers EpCAM, CK7, CK19, AFP, and EFNA1 and up-regulation of mature hepatocyte markers, including albumin, CK8, and CK18. Furthermore, sodium butyrate treatment and a serial passage of HNK1 cells resulted in enhanced albumin secretion, ureagenesis, and CYP enzyme activity, all of which are indicators of differentiation in hepatocytes. However, HNK1 cells at passage 50 did not exhibit anchorage-independent growth capability and caused no tumors in immunodeficient mice, suggesting that they had no spontaneous malignant transformation ability. From this evidence, HNK1 cells were found to be EpCAM(+)/CD133(-) hepatic progenitor cells without spontaneous malignant transformation ability. We therefore conclude that HNK1 cells could be useful for experimental and therapeutic applications.

Indexed as

AC133 AntigenAnimalsAntigens, CDAntigens, NeoplasmBiomarkersButyric AcidCell Adhesion MoleculesCell DifferentiationCells, CulturedCell SeparationEpithelial Cell Adhesion MoleculeFemaleGlycoproteinsHumansLiverLiver CirrhosisAC133 AntigenAntigens, CDAntigens, NeoplasmBiomarkersButyric AcidCell Adhesion MoleculesEpithelial Cell Adhesion MoleculeGlycoproteinsPeptidesPROM1 protein, humanProm1 protein, mouse

Identifiers

PMID24293012
PMCPMC3887933
OpenAlexW1988504408

What OpenQuestion holds

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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.