Pathological and molecular biological approaches to early mesothelioma

Int J Clin Oncol. 2012 Feb;17(1):40-7. doi: 10.1007/s10147-011-0369-1. Epub 2012 Jan 12.


Malignant mesothelioma is an asbestos-related malignancy that arises primarily from mesothelial cells on the serosal surfaces of the pleural, peritoneal, and pericardial cavities. Malignant pleural mesothelioma (MPM) is most common, and its incidence is dramatically increasing worldwide as a result of widespread use of asbestos. Morphological discrimination between MPM and reactive mesothelial hyperplasia is difficult, and the most reliable pathological criterion for malignancy is mesothelial proliferation invading deeply into subpleural adipose tissues. To establish radical cure of MPM, it is crucial to find early-stage MPM of epithelial type, in which mesothelial proliferation is localized on the serosal surface of parietal pleura or limited within the submesothelial fibrous tissues of parietal pleura. The initial clinical presentation for patients with MPM is frequently dyspnea and/or chest pain due to large pleural effusion, and cytological analysis of pleural effusions is valuable to find patients with early-stage MPM of epithelial type. Recently, cytological features of MPM in pleural effusion, molecular markers for MPM, and genetic alternations of MPM have been reported. In this review, we discuss major issues on pathological and molecular biological approaches for diagnosis of early-stage MPM of epithelial type.

Publication types

  • Review

MeSH terms

  • Biomarkers, Tumor / genetics
  • Biomarkers, Tumor / metabolism*
  • Early Detection of Cancer*
  • Genes, p16
  • Humans
  • Mesothelioma / genetics
  • Mesothelioma / metabolism*
  • Mesothelioma / pathology*
  • Neoplasm Staging
  • Neurofibromin 2 / genetics
  • Neurofibromin 2 / metabolism
  • Pleural Effusion, Malignant / pathology
  • Pleural Neoplasms / genetics
  • Pleural Neoplasms / metabolism*
  • Pleural Neoplasms / pathology*
  • Tumor Suppressor Proteins / genetics
  • Tumor Suppressor Proteins / metabolism
  • Ubiquitin Thiolesterase / genetics
  • Ubiquitin Thiolesterase / metabolism


  • BAP1 protein, human
  • Biomarkers, Tumor
  • Neurofibromin 2
  • Tumor Suppressor Proteins
  • Ubiquitin Thiolesterase