| Literature DB >> 24576622 |
Giacomo Cossa1, Cinzia Lanzi1, Giuliana Cassinelli1, Nives Carenini1, Noemi Arrighetti1, Laura Gatti1, Elisabetta Corna1, Franco Zunino1, Nadia Zaffaroni1, Paola Perego2.
Abstract
Deregulated pro-survival signalling plays a role in ovarian carcinoma drug resistance. Here, we show that cisplatin or oxaliplatin in combination with the MEK1/2 inhibitor CI-1040 resulted in a synergistic effect associated with enhanced apoptotic response in platinum-sensitive cells. The drug combinations were additive in platinum-resistant cells exhibiting increased phospho-ERK1/2, down-regulation of apoptosis-related factors (BAX, PUMA, FOXO1) and of phosphatases inhibiting ERK1/2 (DUSP5, DUSP6). Consistently, FOXO1 knockdown in sensitive cells reduced the efficacy of the combination treatment. Pharmacological targeting of ERK1/2 pathway increases cell sensitivity to platinum compounds by interfering with multiple events, ultimately favouring apoptosis induction in selected molecular backgrounds.Entities:
Keywords: Drug resistance; FOXO1; MEK inhibitors; Ovarian carcinoma; Platinum compounds
Mesh:
Substances:
Year: 2014 PMID: 24576622 DOI: 10.1016/j.canlet.2014.02.016
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679