| Literature DB >> 25663936 |
Ulyana Muñoz Acuña1, Nighat Fatima2, Safia Ahmed3, Leng Chee Chang4, Esperanza J Carcache de Blanco1.
Abstract
Nuclear factor κappa-B inhibitors isolated from natural sources that induce apoptosis are promising new agents with anticancer properties. Wortmannin and wortmannolone were isolated from endophytic fungus (Penicillum polonicum) and showed NF-κB inhibitory effects with inhibitory concentration (IC50) of 0.47 μM and 2.06 μM for wortmannin and wortmannolone, respectively. The activity was compared with rocaglamide (IC50=0.075 μM). The mechanism through which wortmannin and wortmannolone exhibited an attenuating effect on the NF-κB pathway was further evaluated in this study. Wortmannolone showed significant reactive oxygen species (ROS) inducing effects in HeLa cervical cells. The ROS inducing effect was concentration dependent, and the ROS generating activity was comparable with daunomycin, a potent chemotherapeutic agent. The findings suggested that the elevated formation of ROS was partially involved in the induction of apoptosis in treated cells. Potent cytotoxic and apoptotic effects were also displayed in MDA-MB-231 hormone independent breast cancer cells when treated with wortmannolone (IC50=3.79 nM). Thus, wortmannolone, a furanosteroid from an endophytic fungus, is a promising agent for further drug development.Entities:
Keywords: K-Ras and NF-κB mediated pathways; Reactive oxygen species; apoptosis; combination index; furanosteroids; synergy; wortmannolone
Year: 2013 PMID: 25663936 PMCID: PMC4318515
Source DB: PubMed Journal: Int J Cancer Res (Tortola) ISSN: 2051-784X