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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
Biomarkers for Malignant Pleural Mesothelioma-A Novel View on Inflammation
Melanie Vogl1, Anna Rosenmayr1, Tomas Bohanes1
1Department of General and Thoracic Surgery, Karl Landsteiner University of Health Sciences, University Hospital Krems, 3500 Krems an der Donau, Austria.
Abstract:
Malignant pleural mesothelioma (MPM) is an aggressive disease with limited treatment response and devastating prognosis. Exposure to asbestos and chronic inflammation are acknowledged as main risk factors. Since immune therapy evolved as a promising novel treatment modality, we want to reevaluate and summarize the role of the inflammatory system in MPM. This review focuses on local tumor associated inflammation on the one hand and systemic inflammatory markers, and their impact on MPM outcome, on the other hand. Identification of new biomarkers helps to select optimal patient tailored therapy, avoid ineffective treatment with its related side effects and consequently improves patient's outcome in this rare disease. Additionally, a better understanding of the tumor promoting and tumor suppressing inflammatory processes, influencing MPM pathogenesis and progression, might also reveal possible new targets for MPM treatment. After reviewing the currently available literature and according to our own research, it is concluded that the suppression of the specific immune system and the activation of its innate counterpart are crucial drivers of MPM aggressiveness translating to poor patient outcome.
Insights
Malignant pleural mesothelioma (MPM) involves inflammation. Suppressed specific immunity and activated innate immunity drive MPM aggressiveness and poor patient outcomes, highlighting potential therapeutic targets.
Area of Science:
- Oncology
- Immunology
- Pathology
Background:
- Malignant pleural mesothelioma (MPM) is an aggressive cancer with poor prognosis.
- Asbestos exposure and chronic inflammation are key risk factors for MPM.
- Immune therapy presents a promising treatment avenue for MPM.
Purpose of the Study:
- To reevaluate and summarize the role of the inflammatory system in MPM.
- To analyze local tumor-associated inflammation and systemic inflammatory markers in MPM.
- To identify potential biomarkers and therapeutic targets for MPM.
Main Methods:
- Literature review of current research on inflammation in MPM.
- Analysis of local and systemic inflammatory processes.
- Evaluation of the impact of inflammation on MPM pathogenesis and progression.
Main Results:
- Suppression of the specific immune system is observed in MPM.
- Activation of the innate immune system is a crucial driver in MPM.
- These inflammatory shifts correlate with MPM aggressiveness and poor patient outcomes.
Conclusions:
- Inflammatory processes significantly influence MPM pathogenesis and progression.
- Targeting inflammatory pathways may offer new therapeutic strategies for MPM.
- Understanding immune system dynamics is vital for improving MPM patient outcomes.

