Mesothelioma pathophysiology

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Feham Tariq, MD [2],Sujit Routray, M.D. [3]

Overview[edit | edit source]

Asbestos causes DNA damage directly by mechanically interfering with the segregation of chromosomes during mitosis and indirectly by inducing mesothelial cells and macrophages, to release mutagenic reactive oxygen and nitrogen species. Asbestos fibres have been shown to alter the function and secretory properties of macrophages, ultimately creating conditions which favor the development of mesothelioma. Following asbestos phagocytosis, macrophages generate increased amounts of hydroxyl radicals, which are normal by-products of cellular anaerobic metabolism. However, these free radicals are also known clastogenic and membrane-active agents thought to promote asbestos carcinogenicity. These oxidants can participate in the oncogenic process by directly and indirectly interacting with DNA, modifying membrane-associated cellular events, including oncogene activation and perturbation of cellular antioxidant defences. Genes involved in the pathogenesis of mesothelioma include BAP1, CDKN2A, WT1, NF2, and TP53. On gross pathology, pleural mesothelioma is characterized by discrete plaques and nodules that coalesce to produce a sheet-like tumor, with the pleural surface seeding of malignant mesothelioma cells. Based on the histology, mesothelioma may be classified into 3 subtypes: epithelial, sarcomatoid, and biphagic. Mesothelioma is demonstrated by positivity to tumor markers, such as calretinin, epithelial membrane antigen, cytokeratin, and mesothelin.

Pathogenesis[edit | edit source]

The pathogenesis of mesothelioma is influenced by the following factors:^[1][2][3][4]

• Asbestos fibres
• Radiation therapy
• Smoking

Types of Asbestos fibres[edit | edit source]

There are two types of asbestos fibers:

• Amphibole (sharp, rod-like)
• Serpentine

Role of Asbestos fibers[edit | edit source]

Asbestos fibers play the following role in the development of mesothelioma:

• The most common type of fibres found in US are the serpentine fibers, which are considered less carcinogenic than the amphibole ones.
• Following inhalation from the environment, these fibres are trapped in the lower third zone of the lung.
• They are phagocytosed by the mesothelial cells and initiate an oncogenic cascade of events which include:
  • Activation of c-Myc and c-Jun oncogene
  • Promotion of antiapoptotic genes such as Bcl-xL
  • Binding with epidermal growth factor receptor (EGFR)

• Asbestos causes DNA damage directly by mechanically interfering with the segregation of chromosomes during mitosis and indirectly by inducing mesothelial cells and macrophages, to release mutagenic reactive oxygen and nitrogen species.
• Asbestos fibres have been shown to alter the function and secretory properties of macrophages, ultimately creating conditions which favor the development of mesothelioma.
• Following asbestos phagocytosis, macrophages generate increased amounts of hydroxyl radicals, which are normal by-products of cellular anaerobic metabolism.
• However, these free radicals are also known clastogenic and membrane-active agents thought to promote asbestos carcinogenicity. These oxidants can participate in the oncogenic process by directly and indirectly interacting with DNA, modifying membrane-associated cellular events, including oncogene activation and perturbation of cellular antioxidant defences.
• The mesothelium consists of a single layer of flattened to cuboidal cells forming the epithelial lining of the serous cavities of the body including the peritoneal, pericardial and pleural cavities.
• Deposition of asbestos fibres in the parenchyma of the lung may result in the penetration of the visceral pleura from where the fibre can then be carried to the pleural surface, thus leading to the development of malignant mesothelial plaques.
• The processes leading to the development of peritoneal mesothelioma remain unresolved, although it has been proposed that asbestos fibres from the lung are transported to the abdomen and associated organs via the lymphatic system.
• Additionally, asbestos fibres may be deposited in the gut after ingestion of sputum contaminated with asbestos fibres.
• Asbestos also may possess immunosuppressive properties. For example, chrysotile fibres have been shown to depress the in-vitro proliferation of phytohemagglutinin-stimulated peripheral blood lymphocytes, suppress natural killer cell lysis, and significantly reduce lymphokine-activated killer cell viability and recovery.
• Furthermore, genetic alterations in asbestos-activated macrophages may result in the release of potent mesothelial cell mitogens such as platelet-derived growth factor (PDGF) and transforming growth factor-β (TGF-β) which in turn, may induce the chronic stimulation and proliferation of mesothelial cells after injury by asbestos fibres.

Radiation therapy[edit | edit source]

Survivors of radiation therapy have been found to develop mesothelioma according to several studies. Following cancers have been studied post-radiation therapy which are seen to develop mesothelioma:^[5][6][7]

• Non-Hodgkins lymphoma^[8]
• Testicular cancer
• Breast cancer

Smoking[edit | edit source]

• Smoking has a synergistic effect on asbestos fibre inhalation in the pathogenesis of mesothelioma.

Genetics[edit | edit source]

• Development of mesothelioma is the result of multiple genetic mutations.
• Genes involved in the pathogenesis of mesothelioma include:^{[9][10][11][12][13][14]}

• BAP1
• CDKN2A
• WT1
• NF2
• TP53
• PTEN
• MSLN
• LATS2

• Asbestos has also been shown to mediate the entry of foreign DNA into target cells. Incorporation of this foreign DNA may lead to mutations and oncogenesis, by several possible mechanisms:

• Inactivation of tumor suppressor genes
• Activation of oncogenes
• Activation of proto-oncogenes due to incorporation of foreign DNA containing a promoter region
• Activation of DNA repair enzymes, which may be prone to error
• Activation of telomerase
• Prevention of apoptosis

Gross Pathology[edit | edit source]

The following features are seen on gross pathology of mesothelioma:^[15]

• On gross pathology, pleural mesothelioma is characterized by discrete plaques and nodules that coalesce to produce a sheet-like tumor, with the pleural surface seeding of malignant mesothelioma cells.
• The growth usually starts at the inferior margins of the pleura and may invade the diaphragm.
• The lung and interlobar fissures may also be involved.

Gallery[edit | edit source]

• 

  _{Mesothelioma completely encasing the lung.<ref name=grosspictureofmesotheliomaimage1>Image courtesy of Dr. Yale Rosen. Radiopaedia (original file here). Creative Commons BY-SA-NC}

Microscopic Pathology[edit | edit source]

Based on the histology, mesothelioma may be classified into 3 subtypes:^[16]

• Epithelial
• Sarcomatoid
• Biphasic (mixed)

Immunohistochemistry[edit | edit source]

• The cytological and histological diagnosis can be difficult, with mesothelial hyperplasia and metastatic adenocarcinoma appearing similar. Specific markers may be helpful in the diagnosis of mesothelioma.^[17]
• Mesothelioma is demonstrated by positivity to tumor markers, such as:^[17][18]

• Calretinin
• Epithelial membrane antigen
• Cytokeratin
• Mesothelin
• WT1
• Podoplanin
• Osteopontin
• HBME-1

References[edit | edit source]

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