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Low incidence of SV40-like sequences in ependymal tumours
F J Reuther1, J Löhler, J Herms
1Department of Pathology, University Hospitals of Ulm, Ulm, Germany.
Insights
SV40 virus DNA was detected in only 5% of ependymoma tumors studied, suggesting low prevalence. This finding may indicate varying exposure levels to SV40-contaminated polio vaccines across different countries.
Area of Science:
- Oncology
- Virology
- Epidemiology
Background:
- SV40 (Simian virus 40) is a polyomavirus linked to ependymomas in animal models.
- SV40-contaminated poliovirus vaccines exposed millions between 1955-1963.
- Previous studies reported widely varying SV40 presence in human ependymomas (7-90%).
Purpose of the Study:
- To investigate the prevalence of SV40 sequences in archived ependymal tumors.
- To clarify the controversial association between SV40 and ependymoma development.
Main Methods:
- Analysis of 62 archived ependymal tumors (pediatric and adult) surgically treated between 1990-1999.
- Polymerase Chain Reaction (PCR) and DNA sequencing to detect SV40 subgenomic sequences.
Main Results:
- SV40 sequences were found in 3 out of 62 tumors (5%).
- No SV40 sequences were detected in tumors from patients born between 1920-1960.
- Positive cases represented 7% of grade II and III ependymomas, with identical SV40 DNA sequences.
Conclusions:
- The low incidence (5%) of SV40 in studied ependymomas suggests limited oncogenic role in this cohort.
- Observed prevalence is lower than many previous reports, indicating potential geographical variations.
- Differences in SV40-positive ependymoma rates may correlate with varying exposure to contaminated polio vaccines.
Abstract:
Between 1955 and 1963, millions of children and adults were exposed to SV40-contaminated poliovirus vaccines. The oncogenic potential of this polyomavirus was revealed when intracerebral inoculation of SV40 into newborn hamsters resulted in the development of ependymomas and choroid plexus papillomas. Subsequently, SV40-like sequences were repeatedly detected in human ependymomas with broadly ranging incidence rates of 7-90%. Most epidemiological studies, however, have not described an increased occurrence of ependymomas. To gain more data on this controversial issue, this study examined 62 archived ependymal tumours from 31 children and 31 adults who underwent surgery between 1990 and 1999. Only three (5%) of the tumours--including 24 classical, 20 anaplastic, and 12 myxopapillary ependymomas; one subependymoma; and five ependymoblastomas--revealed subgenomic SV40 sequences. None of the ependymomas in patients born between 1920 and 1960 demonstrated SV40-like sequences. The positive tumours represent 7% of grade II and III ependymomas (two paediatric and one adult tumour). DNA sequencing of the PCR product revealed identical sequences of SV40 in the positive ependymal tumours. Compared with the results from other countries, this incidence rate is relatively low. Therefore, it seems likely that significant differences between individual countries exist regarding the prevalence of SV40-positive ependymomas. These differences may reflect different degrees of exposure to SV40-contaminated polio vaccine.
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