Cancer stem cell markers in pediatric sarcomas: Sox2 is associated with tumorigenicity in immunodeficient mice
Language English Country United States Media print-electronic
Document type Comparative Study, Journal Article
PubMed
26790443
DOI
10.1007/s13277-016-4837-0
PII: 10.1007/s13277-016-4837-0
Knihovny.cz E-resources
- Keywords
- Cancer stem cells, Markers, Pediatric sarcomas, Sox2, Tumorigenicity,
- MeSH
- ATP Binding Cassette Transporter, Subfamily G, Member 2 metabolism MeSH
- AC133 Antigen metabolism MeSH
- Child MeSH
- Adult MeSH
- Humans MeSH
- Adolescent MeSH
- Mice, Inbred NOD MeSH
- Mice, SCID MeSH
- Mice MeSH
- Cell Transformation, Neoplastic metabolism pathology MeSH
- Biomarkers, Tumor metabolism MeSH
- Cell Line, Tumor MeSH
- Neoplastic Stem Cells metabolism pathology MeSH
- Neoplasm Proteins metabolism MeSH
- Nestin metabolism MeSH
- Osteosarcoma metabolism pathology MeSH
- Child, Preschool MeSH
- Rhabdomyosarcoma metabolism pathology MeSH
- Sarcoma metabolism pathology MeSH
- SOXB1 Transcription Factors metabolism MeSH
- Animals MeSH
- Check Tag
- Child MeSH
- Adult MeSH
- Humans MeSH
- Adolescent MeSH
- Male MeSH
- Mice MeSH
- Child, Preschool MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Comparative Study MeSH
- Names of Substances
- ATP Binding Cassette Transporter, Subfamily G, Member 2 MeSH
- ABCG2 protein, human MeSH Browser
- AC133 Antigen MeSH
- Biomarkers, Tumor MeSH
- Neoplasm Proteins MeSH
- Nestin MeSH
- PROM1 protein, human MeSH Browser
- SOX2 protein, human MeSH Browser
- SOXB1 Transcription Factors MeSH
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.
Department of Experimental Biology School of Science Masaryk University Brno Czech Republic
Department of Histology and Embryology School of Medicine Masaryk University Brno Czech Republic
International Clinical Research Center St Anne's University Hospital Brno Brno Czech Republic
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