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

被引:28
作者
Frizzell, Kristine M. [1 ,2 ]
Kraus, W. Lee [1 ,2 ,3 ]
机构
[1] Cornell Univ, Dept Mol Biol & Genet, Ithaca, NY 14853 USA
[2] Cornell Univ, Grad Field Biochem Mol & Cell Biol, Ithaca, NY 14853 USA
[3] Cornell Univ, Weill Med Coll, Dept Pharmacol, New York, NY 10021 USA
来源
BREAST CANCER RESEARCH | 2009年 / 11卷 / 06期
关键词
POLY(ADP-RIBOSE) POLYMERASE; GENE;
D O I
10.1186/bcr2451
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
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页数:2
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