Evidence map›Paper›PMID 26790443›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2016

Cancer stem cell markers in pediatric sarcomas: Sox2 is associated with tumorigenicity in immunodeficient mice.

Jan Skoda, Alena Nunukova, Tomas Loja, Iva Zambo, Jakub Neradil, Peter Mudry, Karel Zitterbart, Marketa Hermanova, Ales Hampl, Jaroslav Sterba and 1 more

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2016. 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
1.7field-weighted citation impact, top 14% 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, 33 citations in OpenAlex.

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  17. Unraveling the journey of cancer stem cells from origin to metastasis.Biochimica et biophysica acta. Reviews on cancer · 2019
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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

11 authors at 3 institutions in 1 country.

Jan SkodaDepartment of Experimental Biology, School of Science, Masaryk University, Brno, Czech Republic.
Alena NunukovaDepartment of Experimental Biology, School of Science, Masaryk University, Brno, Czech Republic.
Tomas LojaDepartment of Experimental Biology, School of Science, Masaryk University, Brno, Czech Republic.
Iva Zambo1st Institute of Pathologic Anatomy, St. Anne's University Hospital and School of Medicine, Masaryk University, Brno, Czech Republic.
Jakub NeradilDepartment of Experimental Biology, School of Science, Masaryk University, Brno, Czech Republic.
Peter MudryDepartment of Pediatric Oncology, University Hospital Brno and School of Medicine, Masaryk University, Brno, Czech Republic.
Karel ZitterbartDepartment of Pediatric Oncology, University Hospital Brno and School of Medicine, Masaryk University, Brno, Czech Republic.
Marketa Hermanova1st Institute of Pathologic Anatomy, St. Anne's University Hospital and School of Medicine, Masaryk University, Brno, Czech Republic.
Ales HamplDepartment of Histology and Embryology, School of Medicine, Masaryk University, Brno, Czech Republic.
Jaroslav SterbaDepartment of Pediatric Oncology, University Hospital Brno and School of Medicine, Masaryk University, Brno, Czech Republic.
Renata VeselskaDepartment of Experimental Biology, School of Science, Masaryk University, Brno, Czech Republic. veselska@sci.muni.cz.
Masaryk University · CZSt. Anne's University Hospital Brno · CZUniversity Hospital Brno · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The three most frequent pediatric sarcomas, i.e., Ewing's sarcoma, osteosarcoma, and rhabdomyosarcoma, were examined in this study: three cell lines derived from three primary tumor samples were analyzed from each of these tumor types. Detailed comparative analysis of the expression of three putative cancer stem cell markers related to sarcomas-ABCG2, CD133, and nestin-was performed on both primary tumor tissues and corresponding cell lines. The obtained results showed that the frequency of ABCG2-positive and CD133-positive cells was predominantly increased in the respective cell lines but that the high levels of nestin expression were reduced in both osteosarcomas and rhabdomyosarcomas under in vitro conditions. These findings suggest the selection advantage of cells expressing ABCG2 or CD133, but the functional tests in NOD/SCID gamma mice did not confirm the tumorigenic potential of cells harboring this phenotype. Subsequent analysis of the expression of common stem cell markers revealed an evident relationship between the expression of the transcription factor Sox2 and the tumorigenicity of the cell lines in immunodeficient mice: the Sox2 levels were highest in the two cell lines that were demonstrated as tumorigenic. Furthermore, Sox2-positive cells were found in the respective primary tumors and all xenograft tumors showed apparent accumulation of these cells. All of these findings support our conclusion that regardless of the expression of ABCG2, CD133 and nestin, only cells displaying increased Sox2 expression are directly involved in tumor initiation and growth; therefore, these cells fit the definition of the cancer stem cell phenotype.

Indexed as

AC133 AntigenAdolescentAdultAnimalsATP Binding Cassette Transporter, Subfamily G, Member 2Biomarkers, TumorCell Line, TumorCell Transformation, NeoplasticChildChild, PreschoolFemaleHumansMaleMiceMice, Inbred NODMice, SCIDABCG2 protein, humanAC133 AntigenATP Binding Cassette Transporter, Subfamily G, Member 2Biomarkers, TumorNeoplasm ProteinsNestinPROM1 protein, humanSOX2 protein, humanSOXB1 Transcription FactorsCancer stem cellsMarkersPediatric sarcomasSox2Tumorigenicity

Identifiers

PMID26790443
OpenAlexW2292009157

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.