| Literature DB >> 27931843 |
Amy Dréan1, Christopher J Lord2, Alan Ashworth3.
Abstract
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 gene mutations through synthetic lethality. However, PARP inhibition also shows considerable promise when used together with other therapeutic agents. Here, we summarise both the pre-clinical and clinical evidence for the utility of such combinations and discuss the future prospects and challenges for PARP inhibitor combinatorial therapies. Copyright ÂEntities:
Keywords: BRCA1; BRCA2; Drug combinations; PARP inhibitor
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Year: 2016 PMID: 27931843 DOI: 10.1016/j.critrevonc.2016.10.010
Source DB: PubMed Journal: Crit Rev Oncol Hematol ISSN: 1040-8428 Impact factor: 6.312