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Published on: December 21, 2019
MicroRNA and mRNA features of malignant pleural mesothelioma and benign asbestos-related pleural effusion
Guntulu Ak1, Sandra C Tomaszek2, Farhad Kosari3
1Department of Chest Diseases, Medical Faculty, Eskisehir Osmangazi University, 26480 Eskisehir, Turkey.
Introduction:
We investigated the expression of microRNAs and mRNAs in pleural tissues from patients with either malignant pleural mesothelioma or benign asbestos-related pleural effusion.
Methods:
Fresh frozen tissues from a total of 18 malignant pleural mesothelioma and 6 benign asbestos-related pleural effusion patients were studied. Expression profiling of mRNA and microRNA was performed using standard protocols.
Results:
We discovered significant upregulation of multiple microRNAs in malignant pleural mesothelioma compared to benign asbestos-related pleural effusion. Hsa-miR-484, hsa-miR-320, hsa-let-7a, and hsa-miR-125a-5p were able to discriminate malignant from benign disease. Dynamically regulated mRNAs were also identified. MET was the most highly overexpressed gene in malignant pleural mesothelioma compared to benign asbestos-related pleural effusion. Integrated analyses examining microRNA-mRNA interactions suggested multiple altered targets within the Notch signaling pathway.
Conclusions:
Specific microRNAs and mRNAs may have diagnostic utility in differentiating patients with malignant pleural mesothelioma from benign asbestos-related pleural effusion. These studies may be particularly helpful in patients who reside in a region with a high incidence of mesothelioma.
Insights
Specific microRNAs and messenger RNAs (mRNAs) show promise in distinguishing malignant pleural mesothelioma from benign asbestos-related pleural effusion, aiding diagnosis in high-incidence areas.
Area of Science:
- Molecular Biology
- Oncology
- Respiratory Medicine
Background:
- Investigated microRNA (miRNA) and mRNA expression in pleural tissues.
- Compared tissues from patients with malignant pleural mesothelioma (MPM) and benign asbestos-related pleural effusion (BAPE).
Purpose of the Study:
- To identify specific miRNAs and mRNAs with diagnostic utility for differentiating MPM from BAPE.
- To explore potential molecular mechanisms underlying MPM development.
Main Methods:
- Analyzed fresh frozen pleural tissues from 18 MPM and 6 BAPE patients.
- Performed expression profiling for both mRNA and miRNA using standard protocols.
Main Results:
- Identified significant upregulation of several miRNAs (hsa-miR-484, hsa-miR-320, hsa-let-7a, hsa-miR-125a-5p) in MPM compared to BAPE.
- Discovered MET as the most overexpressed gene in MPM.
- Integrated analyses revealed altered targets within the Notch signaling pathway through miRNA-mRNA interactions.
Conclusions:
- Specific miRNAs and mRNAs demonstrate diagnostic potential for distinguishing MPM from BAPE.
- Findings may be particularly valuable for early diagnosis in high-incidence mesothelioma regions.
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