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Implantation and Monitoring by PET/CT of an Orthotopic Model of Human Pleural Mesothelioma in Athymic Mice
Published on: December 21, 2019
A molecular epidemiology case control study on pleural malignant mesothelioma
Claudia Bolognesi1, Fernanda Martini, Mauro Tognon
1Environmental Carcinogenesis Unit, National Cancer Research Institute, L. go Rosanna Benzsi, 10 Genoa, Italy 16132. claudia.bolognesi@istge.it
Malignant mesothelioma patients show double the micronuclei frequency, indicating increased cytogenetic damage beyond asbestos exposure. This suggests other cofactors contribute to cancer development, highlighting a potential marker for cancer susceptibility.
Area of Science:
- Oncology
- Genetics
- Environmental Health
Background:
- Pleural malignant mesothelioma is rare, typically linked to asbestos, but increasing cases with low exposure suggest cofactors are involved.
- Genetic complexity and accumulated genomic damage are characteristic of mesothelioma.
- The cytokinesis-blocked micronucleus test in peripheral blood lymphocytes (PBL) is a key method for assessing genomic damage and chromosomal instability.
Purpose of the Study:
- To evaluate micronuclei frequency in PBLs of malignant mesothelioma patients compared to lung cancer, healthy, and risk controls.
- To assess micronuclei frequency as a marker of cancer susceptibility.
- To investigate the correlation with Simian Virus 40 (SV40) presence.
Main Methods:
- Biomonitoring study using the cytokinesis-blocked micronucleus test on peripheral blood lymphocytes (PBL).
- Comparison of micronuclei frequency in patients with pleural malignant mesothelioma, lung cancer, healthy controls, and risk controls.
- Analysis for the presence of SV40 DNA sequences in T lymphocytes.
Main Results:
- Malignant mesothelioma patients exhibited significantly increased micronuclei frequency compared to all other groups.
- The mean micronuclei frequency was approximately double in mesothelioma patients versus healthy, risk, and lung adenocarcinoma controls.
- SV40 large T antigen DNA sequences were found at low prevalence in both cancer patients and controls.
Conclusions:
- Elevated micronuclei frequency in mesothelioma patients suggests significant cytogenetic damage.
- This damage may result from exogenous and endogenous cofactors in addition to asbestos exposure.
- Micronuclei frequency in PBLs could serve as a biomarker for cancer susceptibility in mesothelioma.
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