Podoplanin has become a useful immunohistochemical marker for identifying mesothelioma.
Through tissue staining, pathologists use podoplanin to tell the difference between epithelioid mesothelioma and adenocarcinoma — a type of cancer that forms in the mucus-secreting membranes throughout the body.
Podoplanin is better for detecting sarcomatoid mesothelioma than calretinin, another immunohistochemical marker. Sarcomatoid is the least common and hardest-to-treat cell type of malignant mesothelioma.
A 2017 study in Cancer Science discussed podoplanin as a potential target for mesothelioma treatment. Researchers in Japan showed how the protein promotes progression of malignant pleural mesothelioma. Podoplanin regulates tumor motility and focus formation.
What Is Podoplanin?
Podoplanin is a mucin-type transmembrane glycoprotein expressed in normal cells. The protein is expressed naturally in the brain, heart, kidneys and lungs. It is also expressed in osteoblasts (cells that form bones) and lymphoid organs (red bone marrow and the thymus gland).
The exact function of podoplanin is unknown in most of these tissues. Research shows podoplanin plays a role in forming connections between the cardiovascular and lymphatic systems.
While the specific function of this protein has yet to be determined, it has proven useful as a diagnostic marker for several cancers. It is highly expressed in squamous cell carcinomas, malignant mesothelioma and brain tumors.
Podoplanin to Diagnose Mesothelioma
Malignant mesothelioma cells show high expressions of podoplanin. In contrast, podoplanin is not expressed at all in adenocarcinomas of the lung and breast. This makes the protein an important marker in preventing mesothelioma misdiagnosis.
A 2010 study in Diagnostic Cytopathology showed podoplanin is expressed in 94 percent of malignant mesothelioma cases. It is also expressed in 97 percent of cases of reactive mesothelial cells, a common sign of infection or inflammation.
It is difficult to differentiate malignant adenocarcinoma effusions from those of mesothelial cells. Pathologists use podoplanin to find this difference.
The 2010 study concluded podoplanin and calretinin are superior to two other markers — cytokeratin 5/6 and WT-1 — when telling the difference between epithelial mesothelioma and adenocarcinoma.
A 2008 study in The American Journal of Surgical Pathology looked at podoplanin on its own. The researchers found podoplanin is better for detecting sarcomatoid mesothelioma than calretinin.
However, the researchers warned it should be used with caution. No single antibody has demonstrated absolute sensitivity or specificity for sarcomatoid mesothelioma.
Pathologists typically test for several proteins that occur in mesothelioma cells. They also apply other antibodies to check for proteins that are positive markers for other types of cancer, but not mesothelioma.
Other factors in diagnosing mesothelioma include the tumor’s pattern of formation and other features of the cancer cells.
6 Cited Article Sources
The sources on all content featured in The Mesothelioma Center at Asbestos.com include medical and scientific studies, peer-reviewed studies and other research documents from reputable organizations.
Hanna, A. et al. (2010, April). Podoplanin is a useful marker for identifying mesothelioma in malignant effusions.
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Pedgett, D. et al. (2008, January 1). Podoplanin is a Better Immunohistochemical Marker for Sarcomatoid Mesothelioma Than Calretinin.
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Kimura, N. and Kimura, I. (2005), Podoplanin as a marker for mesothelioma. Pathology International, 55: 83-86. doi:10.1111/j.1440-1827.2005.01791.x
Takeuchi, S. et al. (2017, April). Podoplanin promotes progression of malignant pleural mesothelioma by regulating motility and focus formation.
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Chernova, T. et al. (2016, February 19). Molecular profiling reveals primary mesothelioma cell lines recapitulate human disease.
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- Astarita, J., Acton, S. & Turley, S. (2012, September 12). Podoplanin: emerging functions in development, the immune system, and cancer. Retrieved from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3439854/
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Last Modified March 6, 2020