APOBEC3B stratifies ovarian clear cell carcinoma with distinct immunophenotype and prognosis

Br J Cancer. 2023 Jun;128(11):2054-2062. doi: 10.1038/s41416-023-02239-5. Epub 2023 Mar 30.

Abstract

Background: Ovarian clear cell carcinoma (OCCC) is a challenging disease due to its intrinsic chemoresistance. Immunotherapy is an emerging treatment option but currently impeded by insufficient understanding of OCCC immunophenotypes and their molecular determinants.

Methods: Whole-genome sequencing on 23 pathologically confirmed patients was employed to depict the genomic profile of primary OCCCs. APOBEC3B expression and digital pathology-based Immunoscore were assessed by performing immunohistochemistry and correlated with clinical outcomes.

Results: An APOBEC-positive (APOBEC+) subtype was identified based on the characteristic mutational signature and prevalent kataegis events. APOBEC + OCCC displayed favourable prognosis across one internal and two external patient cohorts. The improved outcome was ascribable to increased lymphocytic infiltration. Similar phenomena of APOBEC3B expression and T-cell accumulation were observed in endometriotic tissues, suggesting that APOBEC-induced mutagenesis and immunogenicity could occur early during OCCC pathogenesis. Corroborating these results, a case report was presented for an APOBEC + patient demonstrating inflamed tumour microenvironment and clinical response to immune checkpoint blockade.

Conclusions: Our findings implicate APOBEC3B as a novel mechanism of OCCC stratification with prognostic value and as a potential predictive biomarker that may inform immunotherapeutic opportunities.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma, Clear Cell* / genetics
  • Carcinoma*
  • Cytidine Deaminase
  • Female
  • Humans
  • Minor Histocompatibility Antigens
  • Mutation
  • Ovarian Neoplasms* / genetics
  • Prognosis
  • T-Lymphocytes / pathology
  • Tumor Microenvironment

Substances

  • APOBEC3B protein, human
  • Cytidine Deaminase
  • Minor Histocompatibility Antigens