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The development of PARP inhibitors in ovarian cancer: from bench to bedside
Yvette Drew1,2
1Northern Institute for Cancer Research, Newcastle University, Newcastle upon Tyne, UK.
Abstract:
The nuclear enzyme poly (ADP-ribose) polymerase (PARP) represents an important novel target in the treatment of ovarian cancer. This article charts over 50 years of research from the discovery of the first PARP enzyme in 1963, to the approval and licensing in 2015 of the first PARP inhibitor, olaparib (Lynparza), in the treatment of BRCA-mutated ovarian cancer.
Insights
Poly (ADP-ribose) polymerase (PARP) inhibitors are a novel treatment for ovarian cancer. Research over 50 years led to the 2015 approval of olaparib for BRCA-mutated ovarian cancer.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- The nuclear enzyme poly (ADP-ribose) polymerase (PARP) has emerged as a significant therapeutic target in ovarian cancer treatment.
- Over five decades of research have elucidated the role of PARP enzymes.
Purpose of the Study:
- To provide a historical overview of PARP research in ovarian cancer.
- To highlight the development and approval of PARP inhibitors.
Main Methods:
- Literature review of PARP enzyme discovery and development of inhibitors.
- Chronological analysis of key research milestones.
Main Results:
- The first PARP enzyme was discovered in 1963.
- The first PARP inhibitor, olaparib (Lynparza), was approved in 2015 for BRCA-mutated ovarian cancer.
Conclusions:
- PARP inhibitors represent a major advancement in ovarian cancer therapy.
- Continued research into PARP pathways may yield further therapeutic strategies.
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