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Updated: May 8, 2026

Murine Model for Non-invasive Imaging to Detect and Monitor Ovarian Cancer Recurrence
Published on: November 2, 2014
Targeting TOP2A in Ovarian Cancer: Biological and Clinical Implications
Fulvio Borella1, Stefano Fucina1, Ylenia Seminara1
1Gynecology and Obstetrics 1U, Department of Surgical Sciences, University of Turin, 10126 Turin, Italy.
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.
Insights
Topoisomerase II alpha (TOP2A) is crucial for ovarian cancer cell growth. Targeting TOP2A offers a promising therapeutic strategy for epithelial ovarian cancer (EOC), potentially overcoming treatment resistance.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Topoisomerase II alpha (TOP2A) is vital for DNA replication and cell proliferation.
- Overexpression of TOP2A in epithelial ovarian cancer (EOC) correlates with poor prognosis and treatment resistance.
Purpose of the Study:
- To review the biological roles of TOP2A in EOC.
- To discuss TOP2A as a therapeutic target for EOC management.
Main Methods:
- Literature review of TOP2A's function in EOC.
- Analysis of mechanisms driving tumor progression and recurrence.
- Evaluation of clinical strategies targeting TOP2A.
Main Results:
- TOP2A overexpression contributes to EOC progression and recurrence.
- TOP2A inhibitors show potential in EOC treatment.
- Combination therapies involving TOP2A inhibitors may enhance efficacy.
Conclusions:
- Targeting TOP2A is a viable strategy for EOC therapy.
- Further research into TOP2A inhibitors and combination treatments is warranted.
- Understanding TOP2A's role is key to improving EOC patient outcomes.
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