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The Combination of the PARP Inhibitor Rucaparib and 5FU Is an Effective Strategy for Treating Acute Leukemias

Authors :
Giovanni Martinelli
Andrea Ghelli Luserna di Rorà
Klaus-Michael Debatin
Francesco Bertolini
Chiara Ronchini
Lüder Hinrich Meyer
P G Pelicci
Mario Faretta
Ilaria Iacobucci
Stefania Orecchioni
Maria Vittoria Verga Falzacappa
Falzacappa, Maria Vittoria Verga
Ronchini, Chiara
Faretta, Mario
Iacobucci, Ilaria
Ghelli Luserna Di Rorà, Andrea
Martinelli, Giovanni
Meyer, Lüder Hinrich
Debatin, Klaus-Michael
Orecchioni, Stefania
Bertolini, Francesco
Pelicci, Pier Giuseppe
Source :
Molecular Cancer Therapeutics. 14:889-898
Publication Year :
2015
Publisher :
American Association for Cancer Research (AACR), 2015.

Abstract

The existing treatments to cure acute leukemias seem to be nonspecific and suboptimal for most patients, drawing attention to the need of new therapeutic strategies. In the last decade the anticancer potential of poly ADP-ribose polymerase (PARP) inhibitors became apparent and now several PARP inhibitors are being developed to treat various malignancies. So far, the usage of PARP inhibitors has been mainly focused on the treatment of solid tumors and not too much about their efficacy on leukemias is known. In this study we test, for the first time on leukemic cells, a combined therapy that associates the conventional chemotherapeutic agent fluorouracil (5FU), used as a source of DNA damage, and a PARP inhibitor, rucaparib. We demonstrate the efficacy and the specificity of this combined therapy in killing both acute myeloid leukemia and acute lymphoid leukemia cells in vitro and in vivo. We clearly show that the inhibition of DNA repair induced by rucaparib is synthetic lethal with the DNA damage caused by 5FU in leukemic cells. Therefore, we propose a new therapeutic strategy able to enhance the cytotoxic effect of DNA-damaging agents in leukemia cells via inhibiting the repair of damaged DNA. Mol Cancer Ther; 14(4); 889–98. ©2015 AACR.

Details

ISSN :
15388514 and 15357163
Volume :
14
Database :
OpenAIRE
Journal :
Molecular Cancer Therapeutics
Accession number :
edsair.doi.dedup.....91b50a31e340742409e9397be74f173d
Full Text :
https://doi.org/10.1158/1535-7163.mct-14-0276