Dual inhibition of ATR and PARP reverses acquired PARP inhibitor resistance in triple negative breast cancer. [PDF]
Guney Eskiler G +3 more
europepmc +1 more source
PARP inhibitor and PRMT5 inhibitor synergy is independent of BRCA1/2 and MTAP status in breast cancer cells. [PDF]
Suresh S, McPherson L, Ford JM.
europepmc +1 more source
Differential PARP inhibitor responses in BRCA1-deficient and resistant cells in competitive co-culture. [PDF]
Soetomo SA, Sharp MF, Crismani W.
europepmc +1 more source
Metabolic subtyping reveals PDIK1L as a dual-functional regulator of progression and PARP inhibitor sensitivity in prostate cancer. [PDF]
Wang Z +10 more
europepmc +1 more source
Comprehensive genomic profiling for homologous recombination deficiency guides PARP inhibitor therapy recommendations in ovarian cancer. [PDF]
Inci A +5 more
europepmc +1 more source
Genetic evidence for PARP1 trapping as a driver of PARP inhibitor efficacy in BRCA mutant cancer cells. [PDF]
Ribeiro J +14 more
europepmc +1 more source
The Real-World Impact of PARP Inhibitor Maintenance Therapy in High Grade Serous Tubo-Ovarian and Peritoneal Cancers. [PDF]
Al-Ani M +15 more
europepmc +1 more source
PARP inhibitor combination therapy
In 2014, olaparib (Lynparza) became the first PARP (Poly(ADP-ribose) polymerase) inhibitor to be approved for the treatment of cancer. When used as single agents, PARP inhibitors can selectively target tumour cells with BRCA1 or BRCA2 tumour suppressor ...
Christopher J Lord, Alan Ashworth
exaly +5 more sources
Related searches:
Poly (ADP-ribose) polymerase (PARP) is a novel therapeutic target in cancer. Preclinical studies demonstrate that PARP inhibitors selectively kill BRCA-deficient cells and potentiate the effects of DNA-damaging agents. There are several PARP inhibitors in clinical development, including olaparib, iniparib, veliparib, PF-01367338, and MK-4827.
Hongyan Liang, Antoinette R. Tan
openaire +2 more sources

