Abstract

Malignant pleural mesothelioma (MPM) is a rare, but severe form of cancer, with an incidence that varies significantly within and among different countries around the world. It develops in about one to two persons per million of the general population, leading to thousands of deaths every year worldwide. To date, the MPM is mostly associated with occupational asbestos exposure. Asbestos represents the predominant etiological factor, with approximately 70% of cases of MPM with well-documented occupational exposure to asbestos, with the exposure time, on average greater than 40 years. Environmental exposure to asbestos is increasingly becoming recognized as a cause of mesothelioma, together with gene mutations. The possible roles of other cofactors, such as viral infection and radiation exposure, are still debated. MPM is a fatal tumor. This cancer arises during its early phase without clinical signs. Consequently, its diagnosis occurs at advanced stages. Standard clinical therapeutic approaches include surgery, chemo- and radiotherapies. Preclinical and clinical researches are making great strides in the field of this deadly disease, identifying new biomarkers and innovative therapeutic approaches. Among the newly identified markers and potential therapeutic targets, circulating microRNAs and the Notch pathway represent promising avenues that could result in the early detection of the tumor and novel therapeutic approaches.

Highlights

  • Malignant pleural mesothelioma (MPM) represents about 80% of mesothelioma cases

  • The aim of this review is to describe currently available therapies and to discuss novel therapeutic targets and/or early detection markers that could be developed based on the dissection of the underlying molecular mechanism involved in the onset and progression of MPM

  • A study has found that 38% of MPM samples displayed Neurofibromin 2 (NF2) gene mutations, and 29.4% displayed deletions, while no NF2 mutations were found in non-small cell lung cancer patients [67]

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Summary

New Perspectives on Diagnosis and Therapy of Malignant Pleural Mesothelioma

Reviewed by: Giovanni Gaudino, Retired, Bellinzona, Switzerland Francine Baumann, University of New Caledonia, France Michele Carbone, University of Hawaii Cancer Center, United States. The MPM is mostly associated with occupational asbestos exposure. Asbestos represents the predominant etiological factor, with approximately 70% of cases of MPM with well-documented occupational exposure to asbestos, with the exposure time, on average greater than 40 years. Environmental exposure to asbestos is increasingly becoming recognized as a cause of mesothelioma, together with gene mutations. This cancer arises during its early phase without clinical signs. Preclinical and clinical researches are making great strides in the field of this deadly disease, identifying new biomarkers and innovative therapeutic approaches. Among the newly identified markers and potential therapeutic targets, circulating microRNAs and the Notch pathway represent promising avenues that could result in the early detection of the tumor and novel therapeutic approaches

INTRODUCTION
MOLECULAR MECHANISMS UNDERLYING MPM
Tumor Suppressor Genes in MPM
Oncogenes in MPM
The Oncogene Notch
Surgical Treatment
Multimodality Therapy
Immunotherapy and Targeted Therapy
NEW THERAPEUTIC APPROACHES AND NOVEL MOLECULAR TARGETS
Circulating Biomarkers of MPM
Targeting the Notch Pathway in MPM
Precision Oncology and Future Directions in the Treatments of MPM Patients
Findings
AUTHOR CONTRIBUTIONS

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