Abstract |
Recent studies of the genomic landscape of salivary gland tumors have provided important insights into the molecular pathogenesis of these tumors. The most consistent alterations identified include a translocation-generated gene fusion network involving transcription factors, transcriptional coactivators, tyrosine kinase receptors, and other kinases. In addition, next-generation sequencing studies of a few subtypes of salivary neoplasms have revealed hotspot mutations in individual genes and mutations clustering to specific pathways frequently altered in cancer. Although limited, these studies have opened up new avenues for improved classification and targeted therapies of salivary gland cancers. In this review, we summarize the latest developments in this field, focusing on tumor types for which clinically important molecular data are available.
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Authors | Mattias K Andersson, Göran Stenman |
Journal | Oral oncology
(Oral Oncol)
Vol. 57
Pg. 63-9
(06 2016)
ISSN: 1879-0593 [Electronic] England |
PMID | 27101980
(Publication Type: Journal Article, Review)
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Copyright | Copyright © 2016 Elsevier Ltd. All rights reserved. |
Chemical References |
- Transcription Factors
- Receptor Protein-Tyrosine Kinases
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Topics |
- Gene Fusion
- Genomics
- Humans
- Mutation
- Receptor Protein-Tyrosine Kinases
(genetics)
- Salivary Gland Neoplasms
(diagnosis, genetics, therapy)
- Transcription Factors
(genetics)
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