Evidence map›Paper›PMID 23638793›Full record

ArticleStem cells and development2013

Efficacy of using cancer stem cell markers in isolating and characterizing liver cancer stem cells.

George S Wilson, Zenan Hu, Wei Duan, Aiping Tian, Xin M Wang, Duncan McLeod, Vincent Lam, Jacob George, Liang Qiao

Open access · hybridAbstract read
In one paragraph

Article in Stem cells and development, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

22 citing papers in PubMed, 53 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. In Vivo Study on the Effects of Xiaoaiping on the Stemness of Hepatocellular Carcinoma Cells.Evidence-based complementary and alternative medicine : eCAM · 2019
    Article
  10. Iron Metabolism in Liver Cancer Stem Cells.Frontiers in oncology · 2019
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. miR-221 regulates CD44 in hepatocellular carcinoma through the PI3K-AKT-mTOR pathway.Biochemical and biophysical research communications · 2017
    Article
  18. Epigenetics in cancer stem cells.Molecular cancer · 2017
    Review
  19. CD133Scientific reports · 2017
    Article
  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

9 authors at 4 institutions in 3 countries.

George S Wilson1 Storr Liver Unit, Westmead Millennium Institute, The University of Sydney and Westmead Hospital , Westmead, Australia .
Zenan Hu
Wei Duan
Aiping Tian
Xin M Wang
Duncan McLeod
Vincent Lam
Jacob George
Liang Qiao
The University of Sydney · AUDeakin University · AUFirst Hospital of Lanzhou University · CNWestmead Hospital · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent evidence suggests that a subset of hepatocellular carcinomas (HCCs) are derived from liver cancer stem cells (LCSCs). In order to isolate and characterize LCSCs, reliable markers that are specific to these cells are required. We evaluated the efficacy of a range of cancer stem cell (CSC) markers in isolating and characterizing LCSCs. We show that the most widely used CSC markers are not specific to LCSCs. By western analysis, protein expression of the common markers showed no significant difference between HCC tumor tissues and adjacent non-cancerous liver. Further, isolation of LCSCs from common HCC cell lines using FACScan and microbeads showed no consistent marker expression pattern. We also show that LCSCs have unique subtypes. Immunohistochemistry of HCC tissues showed that different HCCs express unique combinations of LCSC markers. Quantitative real-time polymerase chain reaction analysis showed that LCSCs isolated using different markers in the same HCC phenotype had different expression profiles. Likewise, LCSCs isolated from different HCC phenotypes with the same marker also had unique expression profiles and displayed varying resistance profiles to Sorafenib. Thus, using a range of commonly used CSC markers in HCCs and cell lines, we demonstrate that currently available markers are not specific for LCSCs. LCSCs have unique subtypes that express distinctive combinations of LCSC markers and altered drug resistance profiles, making their identification problematic.

Indexed as

Drug Resistance, NeoplasmAC133 Antigenalpha-FetoproteinsAntigens, CDAntigens, NeoplasmAntineoplastic AgentsBiomarkers, TumorCarcinoma, HepatocellularCell Adhesion MoleculesCell Line, TumorCell ProliferationEpithelial Cell Adhesion MoleculeGene Expression ProfilingGlycoproteinsHumansHyaluronan ReceptorsAC133 AntigenAFP protein, humanalpha-FetoproteinsAntigens, CDAntigens, NeoplasmAntineoplastic AgentsBiomarkers, TumorCell Adhesion MoleculesEPCAM protein, humanEpithelial Cell Adhesion MoleculeGlycoproteinsHyaluronan ReceptorsNiacinamidePeptidesPhenylurea CompoundsSorafenibThy-1 Antigens

Identifiers

PMID23638793
PMCPMC3780293
OpenAlexW2028025998

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.