Targeting TOP2A in Ovarian Cancer: Biological and Clinical Implications

Curr Oncol. 2024 Dec 20;31(12):8054-8074. doi: 10.3390/curroncol31120594.

Abstract

The enzyme topoisomerase II alpha (TOP2A) plays a critical role in DNA replication and cell proliferation, making it a promising target for cancer therapy. In epithelial ovarian cancer (EOC), TOP2A overexpression is associated with poor prognosis and resistance to conventional treatments. This review explores the biological functions of TOP2A in EOC and discusses its potential as a therapeutic target. We highlight studies on the mechanisms through which TOP2A contributes to tumor progression and recurrence. Additionally, we evaluate the clinical implications of targeting TOP2A, including the use of TOP2A inhibitors and their combination with novel drugs. We provide a comprehensive overview of the current understanding and future directions for targeting TOP2A in the management of EOC.

Keywords: PARPi; TOP2A; anthracyclines; doxorubicin; etoposide; immune checkpoint inhibitors; ovarian cancer; topoisomerase.

Publication types

  • Review

MeSH terms

  • Antigens, Neoplasm
  • Carcinoma, Ovarian Epithelial / drug therapy
  • DNA Topoisomerases, Type II* / metabolism
  • Female
  • Humans
  • Molecular Targeted Therapy / methods
  • Ovarian Neoplasms* / drug therapy
  • Ovarian Neoplasms* / genetics
  • Poly-ADP-Ribose Binding Proteins / genetics
  • Topoisomerase II Inhibitors / pharmacology
  • Topoisomerase II Inhibitors / therapeutic use

Substances

  • DNA Topoisomerases, Type II
  • TOP2A protein, human
  • Poly-ADP-Ribose Binding Proteins
  • Topoisomerase II Inhibitors
  • Antigens, Neoplasm

Grants and funding

This research received no external funding.