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Published on: December 21, 2019
MicroRNA-98 is a prognostic factor for asbestos-induced mesothelioma
Kihun Kim1, Yeji Ko2, Hyeoncheol Oh1
1Department of Occupational and Environmental Medicine, Kosin University Gospel Hospital, Busan, Republic of Korea.
Abstract:
Malignant pleural mesothelioma (MPM) is a type of cancer characterized by a short survival time and poor prognosis. Malignant pleural mesothelioma is most frequently associated with exposure to asbestos and other elongated mineral fibers. The aim of this study was to examine molecular differences between asbestos-exposed and non-exposed MPM patients and assess prognostic significances of molecular factors. Clinical and genetic data were downloaded from Cancer Genome Atlas. To identify the molecular differences, Significant Analysis of Microarray method was used. Prognostic significances of differentially expressed genes were confirmed by using Kaplan-Meier curve with the Log-Rank test. Although mRNAs did not exhibit any significant differences between the two patient groups, nine miRNAs were found to be down-regulated in the asbestos-exposed group. The top five pathways most relevant to the selected miRNAs were extracted through pathway enrichment analysis. Survival analysis revealed that high expression of only hsa-miR-98 was significantly associated with poor prognosis in patients with asbestos-exposed MPM. Evidence suggests that management of the aggressiveness and progression of asbestos-induced MPM may require high levels of hsa-miR-98 due to its tumor-suppressive role. This study might be helpful in enhancing our understanding of the biological mechanisms underlying asbestos-induced MPM and for acquiring greater insights into targeted therapy.Abbreviations: FDR: false discovery rate; MM: malignant mesothelioma; MPM: malignant pleural mesothelioma; mRNA: messenger RNA; miRNA: microRNA; SAM: significance analysis of microarrays; TCGA: the cancer genome atlas.
Insights
This study found nine microRNAs (miRNAs) down-regulated in asbestos-exposed malignant pleural mesothelioma (MPM) patients. High expression of hsa-miR-98 indicates poor prognosis in asbestos-induced MPM.
Area of Science:
- Oncology
- Molecular Biology
- Environmental Health
Background:
- Malignant pleural mesothelioma (MPM) is an aggressive cancer with poor prognosis, strongly linked to asbestos exposure.
- Understanding molecular distinctions between asbestos-exposed and non-exposed MPM is crucial for targeted therapies.
Purpose of the Study:
- To investigate molecular differences between asbestos-exposed and non-exposed MPM patients.
- To identify molecular factors with prognostic significance in MPM.
Main Methods:
- Utilized clinical and genetic data from The Cancer Genome Atlas (TCGA).
- Employed Significance Analysis of Microarrays (SAM) to identify molecular differences.
- Confirmed prognostic significance using Kaplan-Meier curves and Log-Rank tests.
Main Results:
- No significant differences in messenger RNA (mRNA) expression were observed between groups.
- Nine microRNAs (miRNAs) were found to be significantly down-regulated in asbestos-exposed MPM patients.
- High expression of hsa-miR-98 was significantly associated with poor prognosis in asbestos-exposed MPM.
Conclusions:
- Asbestos exposure leads to specific miRNA expression changes in MPM.
- hsa-miR-98 may play a tumor-suppressive role in asbestos-induced MPM.
- Targeting hsa-miR-98 could be a potential therapeutic strategy for asbestos-related MPM.
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