Abstract
To improve the understanding of chemo-refractory high-grade serous ovarian cancers (HGSOCs), we characterized the proteogenomic landscape of 242 (refractory and sensitive) HGSOCs, representing one discovery and two validation cohorts across two biospecimen types (formalin-fixed paraffin-embedded and frozen). We identified a 64-protein signature that predicts with high specificity a subset of HGSOCs refractory to initial platinum-based therapy and is validated in two independent patient cohorts. We detected significant association between lack of Ch17 loss of heterozygosity (LOH) and chemo-refractoriness. Based on pathway protein expression, we identified 5 clusters of HGSOC, which validated across two independent patient cohorts and patient-derived xenograft (PDX) models. These clusters may represent different mechanisms of refractoriness and implicate putative therapeutic vulnerabilities.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 3476-3498.e35 |
| Journal | Cell |
| Volume | 186 |
| Issue number | 16 |
| DOIs | |
| State | Published - Aug 3 2023 |
Bibliographical note
Publisher Copyright:© 2023 The Authors
Keywords
- chemorefractory
- high-grade serous ovarian cancer
- machine learning
- mass spectrometry
- multiple reaction monitoring
- platinum
- precision oncology
- predictive biomarker
- prognostic biomarker
- proteogenomic