Alternate therapeutic pathways for PARP inhibitors and potential mechanisms of resistance

Cancer therapy: Expanding the use of a class of drugs that promote DNA damage PARP inhibitors (PARPi) target a protein called PARP-1 to treat specific types of breast and ovarian cancers with mutations in the BRCA1 and BRCA2 genes, but they may be effective against even more cancers. W. Lee Kraus at the University of Texas Southwestern Medical Center, Dallas, USA, and co-workers review how PARPi work, including mechanisms of action, ongoing clincal trials, and combination therapies. They report that PARPi, acting through PARP-1, function by inhibiting DNA repair and causing replication stress, thereby promoting DNA damage and marking cancer cells for destruction. However, cancers develop resistance to PARPi; further research is needed to determine how these drugs can be used to optimize their efficacy. Improving our understanding of how PARPi function could help to guide wider application of these powerful cancer therapeutics. Homologous recombination (HR) repair deficiency impairs the proper maintenance of genomic stability, thus rendering cancer cells vulnerable to loss or inhibition of DNA repair proteins, such as poly(ADP-ribose) polymerase-1 (PARP-1). Inhibitors of nuclear PARPs are effective therapeutics for a number of different types of cancers. Here we review key concepts and current progress on the therapeutic use of PARP inhibitors (PARPi). PARPi selectively induce synthetic lethality in cancer cells with homologous recombination deficiencies (HRDs), the most notable being cancer cells harboring mutations in the BRCA1 and BRCA2 genes. Recent clinical evidence, however, shows that PARPi can be effective as cancer therapeutics regardless of BRCA1/2 or HRD status, suggesting that a broader population of patients might benefit from PARPi therapy. Currently, four PARPi have been approved by the Food and Drug Administration (FDA) for the treatment of advanced ovarian and breast cancer with deleterious BRCA mutations. Although PARPi have been shown to improve progression-free survival, cancer cells inevitably develop resistance, which poses a significant obstacle to the prolonged use of PARP inhibitors. For example, somatic BRCA1/2 reversion mutations are often identified in patients with BRCA1/2-mutated cancers after treatment with platinum-based therapy, causing restoration of HR capacity and thus conferring PARPi resistance. Accordingly, PARPi have been studied in combination with other targeted therapies to overcome PARPi resistance, enhance PARPi efficacy, and sensitize tumors to PARP inhibition. Moreover, multiple clinical trials are now actively underway to evaluate novel combinations of PARPi with other anticancer therapies for the treatment of PARPi-resistant cancer. In this review, we highlight the mechanisms of action of PARP inhibitors with or without BRCA1/2 defects and provide an overview of the ongoing clinical trials of PARPi. We also review the current progress on PARPi-based combination strategies and PARP inhibitor resistance.

Automated summary

PARPi target PARP-1 protein to cause DNA damage in cancer cells, but resistance can develop, requiring further research for optimization. They can also be effective against other cancers, and ongoing clinical trials are evaluating combination therapies and resistance mechanisms.