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Acta Pharmaceutica Sinica ; (12): 655-660, 2013.
Article in Chinese | WPRIM | ID: wpr-235614

ABSTRACT

The poly(ADP-ribose) polymerases (PARPs) is an important group of enzymes in DNA repair pathways, especially the base excision repair (BER) for DNA single-strand breaks (SSBs) repair. Inhibition of PARP in DNA repair-defective tumors (like those with BRAC1/2 mutations) can lead to cell death and genomic instability, what is so called "synthetic lethality". Currently, PARP inhibitors combined with cytotoxic chemotherapeutic agents in the treatment of BRCA-1/2 deficient cancers are in the clinical development. In this review, we will be focused on the development of combination application of PARP inhibitors with other anticancer agents in clinical trials.


Subject(s)
Animals , Female , Humans , Antineoplastic Agents , Therapeutic Uses , Benzimidazoles , Therapeutic Uses , Breast Neoplasms , Drug Therapy , Genetics , DNA Repair , Drug Therapy, Combination , Enzyme Inhibitors , Therapeutic Uses , Indoles , Therapeutic Uses , Melanoma , Drug Therapy , Mutation , Ovarian Neoplasms , Drug Therapy , Genetics , Phthalazines , Therapeutic Uses , Piperazines , Therapeutic Uses , Poly(ADP-ribose) Polymerase Inhibitors
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