Abstract
Sarcomas are rare mesenchymal malignancies arising in the soft tissues or bone that are known to be genetically diverse and notoriously difficult to treat. Advances in genomics fueled by massively parallel methods such as next-generation sequencing and array technologies have facilitated integrative analyses of genetic alterations with expression and clinical data, heralding opportunities for leveraging targeted therapies in the management of this challenging family of diseases. This chapter discusses how genomic progress has elevated understanding of the molecular mechanisms of sarcoma and its association with heritable cancer predisposition syndromes as well as the therapeutic implications consequent to this new knowledge.
Original language | English |
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Title of host publication | Oncogenomics |
Subtitle of host publication | From Basic Research to Precision Medicine |
Publisher | Elsevier |
Pages | 609-621 |
Number of pages | 13 |
ISBN (Electronic) | 9780128117859 |
ISBN (Print) | 9780128117866 |
DOIs | |
Publication status | Published - Jan 1 2018 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2019 Elsevier Inc. All rights reserved.
ASJC Scopus Subject Areas
- General Medicine
Keywords
- Bone sarcoma
- Cancer predisposition syndromes
- Molecular genetics
- Soft tissue sarcoma
- Targeted therapy