Evidence map›Paper›PMID 25977066›Full record

ArticleInternational journal of molecular medicine2015

Atypical nuclear localization of CD133 plasma membrane glycoprotein in rhabdomyosarcoma cell lines.

Alena Nunukova, Jakub Neradil, Jan Skoda, Josef Jaros, Ales Hampl, Jaroslav Sterba, Renata Veselska

Open access · hybridAbstract read
In one paragraph

Article in International journal of molecular medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

19 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Can CD133 Be Regarded as a Prognostic Biomarker in Oncology: Pros and Cons.International journal of molecular sciences · 2023
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Nuclear CD133 expression predicts poor prognosis for hepatocellular carcinoma.International journal of clinical and experimental pathology · 2018
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Cancer stem cell markers in pediatric sarcomas: Sox2 is associated with tumorigenicity in immunodeficient mice.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
  18. Article
  19. 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 1 country.

Alena NunukovaDepartment of Experimental Biology, Faculty of Science, Masaryk University, 61137 Brno, Czech Republic.
Jakub NeradilDepartment of Experimental Biology, Faculty of Science, Masaryk University, 61137 Brno, Czech Republic.
Jan SkodaDepartment of Experimental Biology, Faculty of Science, Masaryk University, 61137 Brno, Czech Republic.
Josef JarosDepartment of Histology and Embryology, Faculty of Medicine, Masaryk University, 61137 Brno, Czech Republic.
Ales HamplDepartment of Histology and Embryology, Faculty of Medicine, Masaryk University, 61137 Brno, Czech Republic.
Jaroslav SterbaRegional Centre for Applied Molecular Oncology, Masaryk Memorial Cancer Institute, 61137 Brno, Czech Republic.
Renata VeselskaDepartment of Experimental Biology, Faculty of Science, Masaryk University, 61137 Brno, Czech Republic.
Masaryk University · CZMasaryk Memorial Cancer Institute · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CD133 (also known as prominin-1) is a cell surface glycoprotein that is widely used for the identification of stem cells. Furthermore, its glycosylated epitope, AC133, has recently been discussed as a marker of cancer stem cells in various human malignancies. During our recent experiments on rhabdomyosarcomas (RMS), we unexpectedly identified an atypical nuclear localization of CD133 in a relatively stable subset of cells in five RMS cell lines established in our laboratory. To the best of our knowledge, this atypical localization of CD133 has not yet been proven or analyzed in detail in cancer cells. In the present study, we verified the nuclear localization of CD133 in RMS cells using three independent anti-CD133 antibodies, including both rabbit polyclonal and mouse monoclonal antibodies. Indirect immunofluorescence and confocal microscopy followed by software cross-section analysis, transmission electron microscopy and cell fractionation with immunoblotting were also employed, and all the results undeniably confirmed the presence of CD133 in the nuclei of stable minor subpopulations of all five RMS cell lines. The proportion of cells showing an exclusive nuclear localization of CD133 ranged from 3.4 to 7.5%, with only minor differences observed among the individual anti-CD133 antibodies. Although the role of CD133 in the cell nucleus remains unclear, these results clearly indicate that this atypical nuclear localization of CD133 in a minor subpopulation of cancer cells is a common phenomenon in RMS cell lines.

Indexed as

AC133 AntigenAntibodies, MonoclonalAntigens, CDBiomarkers, TumorCell Line, TumorCell NucleusFluorescent Antibody Technique, IndirectGlycoproteinsHumansMicroscopy, Electron, TransmissionPeptidesRhabdomyosarcomaAC133 AntigenAntibodies, MonoclonalAntigens, CDBiomarkers, TumorGlycoproteinsPeptidesPROM1 protein, humanProm1 protein, mouse

Identifiers

PMID25977066
PMCPMC4494592
OpenAlexW1829170902

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.