PARP inhibitors and the treatment of breast cancer: beyond BRCA1/2?

Breast Cancer Res. 2009;11(6):111. doi: 10.1186/bcr2451. Epub 2009 Nov 26.

Abstract

Poly(ADP-ribose) polymerase (PARP) inhibitors have been explored as therapeutic agents for the treatment of hereditary breast and ovarian cancers harboring mutations in BRCA1 or BRCA2. In a new study, Inbar-Rozensal and colleagues show that phenanthridine-derived PARP inhibitors promote cell cycle arrest and cell death in breast cancer cells lacking BRCA1 and BRCA2 mutations and prevent the growth of tumors from xenografts of these cells in immunocompromised mice. These results suggest a potential broader utility of PARP-1 inhibitors in the treatment of breast cancer, although further mechanistic studies are needed.

Publication types

  • Editorial
  • Comment

MeSH terms

  • Animals
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / enzymology
  • Breast Neoplasms / genetics*
  • Enzyme Inhibitors / pharmacology*
  • Female
  • Genes, BRCA1*
  • Genes, BRCA2*
  • Humans
  • Mice
  • Phenanthridines / pharmacology*
  • Poly (ADP-Ribose) Polymerase-1
  • Poly(ADP-ribose) Polymerase Inhibitors*

Substances

  • Enzyme Inhibitors
  • Phenanthridines
  • Poly(ADP-ribose) Polymerase Inhibitors
  • PARP1 protein, human
  • Poly (ADP-Ribose) Polymerase-1