Compartment-specific multiomic profiling identifies SRC and GNAS as candidate drivers of epithelial-to-mesenchymal transition in ovarian carcinosarcoma

Br J Cancer. 2024 Feb;130(2):327-335. doi: 10.1038/s41416-023-02508-3. Epub 2023 Dec 14.

Abstract

Background: Ovarian carcinosarcoma (OCS) is an exceptionally aggressive and understudied ovarian cancer type harbouring distinct carcinomatous and sarcomatous compartments. Here, we seek to identify shared and compartment-specific events that may represent potential therapeutic targets and candidate drivers of sarcomatous compartment formation through epithelial-to-mesenchymal transition (EMT).

Methods: We performed multiomic profiling (exome sequencing, RNA-sequencing, microRNA profiling) of paired carcinomatous and sarcomatous components in 12 OCS cases.

Results: While paired sarcomatous and carcinomatous compartments demonstrate substantial genomic similarities, multiple loci are recurrently copy number-altered between components; regions containing GNAS and SRC are recurrently gained within the sarcomatous compartment. CCNE1 gain is a common event in OCS, occurring more frequently than in high grade serous ovarian carcinoma (HGSOC). Transcriptomic analysis suggests increased MAPK activity and subtype switching toward poor prognosis HGSOC-derived transcriptomic subtypes within the sarcomatous component. The two compartments show global differences in microRNA profiles, with differentially expressed microRNAs targeting EMT-related genes (SIRT1, ZEB2) and regulators of pro-tumourigenic pathways (TGFβ, NOTCH); chrX is a highly enriched target of these microRNAs and is also frequently deleted across samples. The sarcomatous component harbours significantly fewer CD8-positive cells, suggesting poorer immune engagement.

Conclusion: CCNE1 gain and chrX loss are frequent in OCS. SRC gain, increased GNAS expression and microRNA dysregulation represent potential mechanisms driving sarcomatous compartment formation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carcinosarcoma* / genetics
  • Carcinosarcoma* / metabolism
  • Carcinosarcoma* / pathology
  • Chromogranins / genetics
  • Epithelial-Mesenchymal Transition / genetics
  • Female
  • GTP-Binding Protein alpha Subunits, Gs / genetics
  • Humans
  • MicroRNAs* / genetics
  • Multiomics
  • Ovarian Neoplasms* / pathology
  • Sarcoma*

Substances

  • MicroRNAs
  • GNAS protein, human
  • Chromogranins
  • GTP-Binding Protein alpha Subunits, Gs