Frontiers in Oncology (Oct 2023)

Similarities and differences in gene expression profiles of BRCA1 methylated and mutated epithelial ovarian cancers

  • Nora Sahnane,
  • Nora Sahnane,
  • Laura Libera,
  • Laura Libera,
  • Sofia Facchi,
  • Sofia Facchi,
  • Ileana Carnevali,
  • Ileana Carnevali,
  • Susanna Ronchi,
  • Susanna Ronchi,
  • Chiara Albeni,
  • Antonella Cromi,
  • Antonella Cromi,
  • Jvan Casarin,
  • Jvan Casarin,
  • Jvan Casarin,
  • Fausto Sessa,
  • Fausto Sessa,
  • Fausto Sessa,
  • Maria Grazia Tibiletti

DOI
https://doi.org/10.3389/fonc.2023.1268127
Journal volume & issue
Vol. 13

Abstract

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IntroductionBRCA1 methylated (BRCA1met) epithelial ovarian cancer (EOC) is a recently defined and not well-investigated subset of neoplasms. To date, no studies have focused on the transcriptional profiles of BRCA1met cases, and, as a matter of fact, we still do not know if this subset of EOCs is similar, and to what extent, to BRCA1 mutated (BRCA1mut) cases.MethodsWe compared a group of 17 BRCA1met cases against 10 BRCA1mut cases using a subset of carefully selected 17 BRCAwt EOCs as a control group.ResultsFirst, BRCA1met cases showed a downregulation of the relative transcript, while this association was not observed for BRCA1mut EOCs. The BRCA1met group exhibited a general upregulation of homologous recombination (HR)-related genes, as well as BRCA1mut. Overall, BRCA1met had a different gene expression profile, characterized by diffuse downregulation, whereas BRCA1mut showed a general upregulation (p < 0.0001). Both BRCA1-defective groups showed a slightly activated immune response mediated by interferon (IFN) gamma pathways.DiscussionIn conclusion, even if the expression profile of many genes related to DNA damage and repair system is shared between BRCA1mut and BRCA1met EOCs supporting that BRCA1met EOCs may benefit from PARPi therapies, our data demonstrate that BRCA1mut and BRCA1met EOCs show different expression profiles, suggesting a different mechanism of carcinogenesis that can be reflected in different responses to therapies and disease recovery.

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