TY - JOUR
T1 - Predictive biomarkers for cancer therapy with PARP inhibitors
AU - Michels, J.
AU - Vitale, I.
AU - Saparbaev, M.
AU - Castedo, M.
AU - Kroemer, G.
N1 - Funding Information:
The authors would like to thank Lorenzo Galluzzi (Université Paris Descartes, Paris, France) for assistance with manuscript preparation. The authors are supported by the Ligue contre le Cancer (équipe labellisée), Agence National de la Recherche, AXA Chair for Longevity Research, Association pour la Recherche sur le Cancer, Associazione Italiana per la Ricerca sul Cancro (AIRC), Cancéropôle Ile-de-France, Institut National du Cancer (INCa), Fondation Bettencourt-Schueller, Fondation de France, Fondation pour la Recherche Médicale, the European Commission (ArtForce), the European Research Council, the LabEx Immuno-Oncology, Action Lions ‘Vaincre le Cancer’, Luxembourg, the SIRIC Stratified Oncology Cell DNA Repair and Tumor Immune Elimination (Socrate) and Cancer Research and Personalized Medicine (Carpem) and the Paris Alliance of Cancer Research Institutes.
PY - 2014/7/24
Y1 - 2014/7/24
N2 - Poly(ADP-ribose) polymerase (PARP) inhibitors have raised high expectations for the treatment of multiple malignancies. PARP inhibitors, which can be used as monotherapies or in combination with DNA-damaging agents, are particularly efficient against tumors with defects in DNA repair mechanisms, in particular the homologous recombination pathway, for instance due to BRCA mutations. Thus, deficient DNA repair provides a framework for the success of PARP inhibitors in medical oncology. Here, we review encouraging results obtained in recent clinical trials investigating the safety and efficacy of PARP inhibitors as anticancer agents. We discuss emerging mechanisms of regulation of homologous recombination and how inhibition of DNA repair might be used in cancer therapy. We surmise that the identification of patients that are likely to benefit from PARP inhibition will improve the clinical use of PARP inhibitors in a defined target population. Thus, we will place special emphasis on biomarker discovery.
AB - Poly(ADP-ribose) polymerase (PARP) inhibitors have raised high expectations for the treatment of multiple malignancies. PARP inhibitors, which can be used as monotherapies or in combination with DNA-damaging agents, are particularly efficient against tumors with defects in DNA repair mechanisms, in particular the homologous recombination pathway, for instance due to BRCA mutations. Thus, deficient DNA repair provides a framework for the success of PARP inhibitors in medical oncology. Here, we review encouraging results obtained in recent clinical trials investigating the safety and efficacy of PARP inhibitors as anticancer agents. We discuss emerging mechanisms of regulation of homologous recombination and how inhibition of DNA repair might be used in cancer therapy. We surmise that the identification of patients that are likely to benefit from PARP inhibition will improve the clinical use of PARP inhibitors in a defined target population. Thus, we will place special emphasis on biomarker discovery.
UR - http://www.scopus.com/inward/record.url?scp=84904978889&partnerID=8YFLogxK
U2 - 10.1038/onc.2013.352
DO - 10.1038/onc.2013.352
M3 - Review article
C2 - 24037533
AN - SCOPUS:84904978889
SN - 0950-9232
VL - 33
SP - 3894
EP - 3907
JO - Oncogene
JF - Oncogene
IS - 30
ER -