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Published on: December 21, 2019
Molecular Insights into Pleural Mesothelioma: Unveiling Pathogenic Mechanisms and Therapeutic Opportunities
Teodora Zahiu1, Carmen Mihaela Mihu2, Bianca A Bosca2
1Radiology and Imaging Department, County Emergency Hospital, 400006 Cluj-Napoca, Romania.
Abstract:
Pleural mesothelioma (PM) is a rare disease, which is going to be a global medical concern in the 21st century, because of its aggressiveness, late diagnosis, and insufficient therapies. This review seeks to enhance the comprehension of medical professionals regarding the risk factors and environmental influences that contribute to the development of the disease, as well as its underlying mechanisms. In addition, we aim to provide a schematic yet thorough overview of diagnostic techniques in PM, emphasizing the significance of the immunohistochemical markers BAP1 and MTAP, with the latter serving as an almost ideal surrogate for the gold-standard diagnostic approach, FISH p16/CDKN2A deletion. The scientific world is grappling with BAP1, MTAP, and the tumour inflammatory microenvironment, because they are the key for personalized treatments and palliative care in this disease. Considering that the survival rate for patients with PM seldom surpasses five years, every moment is significant. Therefore, our article also highlights recent advancements in clinical assessments related to prognostic scoring and treatment options. PM is a complex disease, with gradual progression over decades, which requires further investigation covering the prevention, mutations, diagnosis and treatment.
Insights
Pleural mesothelioma (PM) is a rare but aggressive cancer. This review details risk factors, diagnostic markers like BAP1 and MTAP, and emerging treatments for this challenging disease.
Area of Science:
- Oncology
- Environmental Medicine
- Pathology
Background:
- Pleural mesothelioma (PM) is an aggressive malignancy with a poor prognosis, posing a growing global health challenge.
- Its rarity, late diagnosis, and limited therapeutic options necessitate a deeper understanding of its development and management.
- Environmental factors and underlying genetic predispositions are key contributors to PM pathogenesis.
Purpose of the Study:
- To enhance medical professionals' understanding of PM risk factors and environmental influences.
- To provide a comprehensive overview of diagnostic modalities, including novel immunohistochemical markers.
- To highlight recent advancements in prognostic scoring and treatment strategies for PM.
Main Methods:
- Review of current literature on pleural mesothelioma epidemiology, pathogenesis, diagnosis, and treatment.
- Emphasis on immunohistochemical markers (BAP1, MTAP) and genetic testing (FISH p16/CDKN2A deletion).
- Analysis of recent clinical trial data and prognostic scoring systems.
Main Results:
- BAP1 and MTAP immunohistochemistry are significant diagnostic tools, with MTAP as a surrogate for FISH p16/CDKN2A deletion.
- The tumor inflammatory microenvironment is crucial for developing personalized treatments.
- Recent advancements offer improved prognostic assessment and therapeutic avenues.
Conclusions:
- A comprehensive understanding of PM's complexity, from environmental triggers to molecular mechanisms, is vital.
- Early diagnosis and personalized treatment strategies targeting BAP1, MTAP, and the tumor microenvironment are critical for improving patient outcomes.
- Continued research into prevention, mutation analysis, diagnosis, and treatment is essential for combating this disease.
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