Abstract
High-grade serous ovarian cancer (HGSC) patients with no gross residual disease (R0) after primary surgery have the greatest improvement in clinical outcomes. A deep understanding of molecular and cellular heterogeneity of HGSC is lacking. Findings by Lee et al. highlight major molecular and cellular differences between clinically defined subgroups of HGSC.
| Original language | English |
|---|---|
| Article number | 107502 |
| Journal | Cell Reports |
| Volume | 31 |
| Issue number | 2 |
| DOIs | |
| State | Published - 14 Apr 2020 |
| Externally published | Yes |
Keywords
- R0 resection
- copy number
- genomics
- immune monitoring
- multi-omics
- mutation
- neoadjuvant chemotherapy
- ovarian cancer
- proteome
- transcriptome