The Role of Molecular Testing in the Differential Diagnosis of Salivary Gland Carcinomas
Language English Country United States Media print
Document type Journal Article, Review
- MeSH
- Biopsy MeSH
- Molecular Diagnostic Techniques * MeSH
- Diagnosis, Differential MeSH
- Phenotype MeSH
- Gene Fusion MeSH
- Genetic Predisposition to Disease MeSH
- Carcinoma genetics pathology therapy MeSH
- Humans MeSH
- Mutation MeSH
- Biomarkers, Tumor genetics MeSH
- Salivary Gland Neoplasms genetics pathology therapy MeSH
- Predictive Value of Tests MeSH
- Neoplasm Grading MeSH
- Translocation, Genetic MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Review MeSH
- Names of Substances
- Biomarkers, Tumor MeSH
Salivary gland neoplasms are a morphologically heterogenous group of lesions that are often diagnostically challenging. In recent years, considerable progress in salivary gland taxonomy has been reached by the discovery of tumor type-specific fusion oncogenes generated by chromosome translocations. This review describes the clinicopathologic features of a selected group of salivary gland carcinomas with a focus on their distinctive genomic characteristics. Mammary analog secretory carcinoma is a recently described entity characterized by a t(12;15)(p13;q25) translocation resulting in an ETV6-NTRK3 fusion. Hyalinizing clear cell carcinoma is a low-grade tumor with infrequent nodal and distant metastasis, recently shown to harbor an EWSR1-ATF1 gene fusion. The CRTC1-MAML2 fusion gene resulting from a t(11;19)(q21;p13) translocation, is now known to be a feature of both low-grade and high-grade mucoepidermoid carcinomas associated with improved survival. A t(6;9)(q22-23;p23-34) translocation resulting in a MYB-NFIB gene fusion has been identified in the majority of adenoid cystic carcinomas. Polymorphous (low-grade) adenocarcinoma and cribriform adenocarcinoma of (minor) salivary gland origin are related entities with partly differing clinicopathologic and genomic profiles; they are the subject of an ongoing taxonomic debate. Polymorphous (low-grade) adenocarcinomas are characterized by hot spot point E710D mutations in the PRKD1 gene, whereas cribriform adenocarcinoma of (minor) salivary glands origin are characterized by translocations involving the PRKD1-3 genes. Salivary duct carcinoma (SDC) is a high-grade adenocarcinoma with morphologic and molecular features akin to invasive ductal carcinoma of the breast, including HER2 gene amplification, mutations of TP53, PIK3CA, and HRAS and loss or mutation of PTEN. Notably, a recurrent NCOA4-RET fusion has also been found in SDC. A subset of SDC with apocrine morphology is associated with overexpression of androgen receptors. As these genetic aberrations are recurrent they serve as powerful diagnostic tools in salivary gland tumor diagnosis, and therefore also in refinement of salivary gland cancer classification. Moreover, they are promising as prognostic biomarkers and targets of therapy.
Coordinator of the International Head and Neck Scientific Group Padua Italy
Department of Anatomical Pathology University of Calgary Foothills Medical Centre Calgary AB Canada
Department of Oncology Section Head and Neck Oncology KU Leuven Leuven Belgium
Department of Pathology Allegiance Health Jackson MI
Department of Pathology University of Arkansas for Medical Sciences Little Rock AR
Department of Pathology University of Texas Southwestern Medical Center Dallas TX
European Salivary Gland Society Geneva Switzerland
Molecular and Genetic Laboratory Biopticka Lab Ltd Plzen Czech Republic
Otorhinolaryngology Head and Neck Surgery University Hospitals Leuven
References provided by Crossref.org
Molecular pathology in diagnosis and prognostication of head and neck tumors
Development of head and neck pathology in Europe
Prognostic significance of 1p36 locus deletion in adenoid cystic carcinoma of the salivary glands
Polymorphous adenocarcinoma of the salivary glands: reappraisal and update