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Intracranial Orthotopic Allografting of Medulloblastoma Cells in Immunocompromised Mice
Published on: October 4, 2010
Medulloblastomas and primitive neuroectodermal tumors rarely contain polyomavirus DNA sequences
John Y H Kim1, Igor J Koralnik, Mark LeFave
1Division of Neuroscience, Department of Neurology, Children's Hospital, Harvard Medical School, 300 Longwood Avenue, Boston, MA 02115, USA.
Abstract:
To address the hypothesis that medulloblastoma or supratentorial primitive neuroectodermal tumor (sPNET) can arise through infection by polyomaviruses, we examined genomic DNA isolated from 15 primary medulloblastoma and 5 sPNET biopsy specimens and from 2 medulloblastoma cell lines for the presence of DNA sequences from the polyomaviruses simian virus 40 (SV40), JC virus, and BK virus. These polyomaviruses have oncogenic potential in animals, and their DNA sequences have been detected in other surveys of various solid tumors, including childhood brain tumors. The tumor DNA samples were analyzed by Southern blot hybridization of polymerase chain reaction products that employed probes designed to detect specific polyomavirus sequences. Neither JC virus nor BK virus DNA sequences were detected in any of the specimens. None of the primary medulloblastoma or sPNET specimens contained SV40 sequences. However, SV40 DNA coding and noncoding sequences were detected in the D283-Med (medulloblastoma) cell line. Immunocytochemical studies of D283-Med revealed nuclear expression of SV40 large T antigen. In contrast to childhood ependymomas and choroid plexus tumors, medulloblastomas and sPNETs infrequently express evidence of polyomavirus infection.
Insights
Polyomavirus infection was investigated as a cause for medulloblastoma and supratentorial primitive neuroectodermal tumors (sPNETs). SV40 DNA was detected in one medulloblastoma cell line, but not in primary tumors.
Area of Science:
- Oncology
- Virology
- Molecular Biology
Background:
- Polyomaviruses, including simian virus 40 (SV40), JC virus, and BK virus, possess oncogenic potential.
- Previous studies have detected polyomavirus DNA in various solid tumors, including pediatric brain tumors.
Purpose of the Study:
- To investigate the hypothesis that medulloblastoma and supratentorial primitive neuroectodermal tumors (sPNETs) may arise from polyomavirus infections.
- To screen for the presence of SV40, JC virus, and BK virus DNA in primary tumor samples and cell lines.
Main Methods:
- Genomic DNA from 15 medulloblastoma and 5 sPNET biopsy specimens, plus 2 medulloblastoma cell lines, was analyzed.
- Southern blot hybridization and polymerase chain reaction (PCR) with specific polyomavirus probes were employed.
Main Results:
- JC virus and BK virus DNA were not detected in any of the analyzed specimens.
- SV40 DNA sequences were absent in all primary medulloblastoma and sPNET samples.
- SV40 DNA (coding and noncoding) and nuclear expression of SV40 large T antigen were identified in the D283-Med cell line.
Conclusions:
- Medulloblastomas and sPNETs infrequently show evidence of polyomavirus infection compared to other pediatric brain tumors like ependymomas.
- While SV40 was not found in primary tumors, its presence in a medulloblastoma cell line warrants further investigation.
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