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SV40 multiple tissue infection and asbestos exposure in a hyperendemic area for malignant mesothelioma
Manola Comar1, Clara Rizzardi, Renata de Zotti
1Department of Public Medicine Sciences, University of Trieste, Trieste, Italy.
Abstract:
To assess the presence of SV40 in malignant mesothelioma tissue, 19 formalin-fixed paraffin-embedded pleural cancer samples of patients from a hyperendemic area of northeastern Italy were analyzed retrospectively. A total of 48 other tissues from the malignant mesothelioma subjects were investigated. The SV40 load was determined by real-time quantitative PCR. Exposure to asbestos was evaluated through a careful review of the occupational history of patients, supplemented by histology and isolation of asbestos bodies. Three of 19 (15.8%) malignant mesothelioma tissues harbored SV40 genomic signals. Two patients with SV40-positive malignant mesothelioma had viral sequences in another tissue. Overall, 3 of 18 (16.7%) normal liver tissues tested positive for SV40, as did 1 of 8 (12.5%) kidney tissues. SV40 viral loads were higher in malignant mesothelioma than in normal cells (P = 0.045). This survey shows that SV40 sustains infections in multiple tissues in malignant mesothelioma patients from a geographic area affected with asbestos-related mesothelioma.
Insights
Simian virus 40 (SV40) was detected in malignant mesothelioma tissues from patients in northeastern Italy. This virus was also found in other tissues, with higher loads in cancer cells, suggesting SV40 sustains infections in mesothelioma patients.
Area of Science:
- Oncology
- Virology
- Environmental Health
Background:
- Malignant mesothelioma is a rare cancer strongly linked to asbestos exposure.
- Simian virus 40 (SV40) has been investigated for its potential role in human cancers, including mesothelioma.
- Previous studies suggest a possible association between SV40 and mesothelioma, but its presence in multiple tissues requires further investigation.
Purpose of the Study:
- To determine the prevalence of SV40 in malignant mesothelioma tissues.
- To investigate the presence of SV40 in other tissues of mesothelioma patients.
- To compare SV40 viral loads in malignant mesothelioma and normal tissues.
Main Methods:
- Retrospective analysis of 19 formalin-fixed paraffin-embedded malignant mesothelioma tissue samples.
- Real-time quantitative PCR (qPCR) to quantify SV40 DNA.
- Evaluation of asbestos exposure through occupational history and histological analysis.
Main Results:
- SV40 genomic signals were detected in 15.8% (3 of 19) of malignant mesothelioma tissues.
- SV40 was also found in other tissues of two patients, including liver (16.7%) and kidney (12.5%).
- SV40 viral loads were significantly higher in malignant mesothelioma tissues compared to normal tissues (P = 0.045).
Conclusions:
- SV40 infection is present in malignant mesothelioma patients from an area endemic for asbestos-related mesothelioma.
- SV40 appears to sustain infections across multiple tissues in these patients.
- The findings support a potential role for SV40 in the pathogenesis of malignant mesothelioma in conjunction with asbestos exposure.
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