Abstract
Cancer genetics is increasingly becoming central in the course of patients’ care. Genetic testing for pathogenic variants in ovarian cancer (OC) is becoming widely available and represents a cornerstone for cancer risk assessment, prediction of prognosis, and targeted treatments. The introduction of novel technologies for sequencing has enabled large-scale multigene panel genomic testing. In this chapter, the current genetic variants and genetic testing guidelines for OC are reviewed. We also discussed potential applications of next-generation sequencing in understanding OC genetics and its impact on patients’ outcomes according to the latest research findings. We finally depict the potential of single-cell sequencing in understanding OC heterogeneity based on recent proof-of-concept studies.
| Original language | English |
|---|---|
| Title of host publication | Ovarian Cancer Biomarkers |
| Subtitle of host publication | Mapping to Improve Outcomes |
| Publisher | Springer Nature |
| Pages | 203-229 |
| Number of pages | 27 |
| ISBN (Electronic) | 9789811618734 |
| ISBN (Print) | 9789811618727 |
| DOIs | |
| State | Published - Jan 1 2021 |
| Externally published | Yes |
ASJC Scopus Subject Areas
- General Medicine
- General Biochemistry,Genetics and Molecular Biology
Keywords
- Genetic testing
- Next-generation sequencing
- Ovarian cancer
- Single-cell sequencing
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