Abstract
Abstract Ovarian cancer is the most lethal of all gynecological cancers. Current treatment of advanced ovarian cancers, which includes debulking surgery and chemotherapy, is initially effective in majority of patients; however, 70-90% of them eventually develop disease recurrence with limited treatment options. This recurrence can be attributed to therapy-resistant cancer stem cells (CSC), which represent a subset of all malignant cells that form the bulk of ovarian cancers. CSC may remain as a minimal residual disease after the bulk of ovarian tumor mass has been removed by surgery and/or chemotherapy; therefore, there is considerable current interest in the development of new therapies that can effectively target this insidious subpopulation of tumor cells. Here we report on the anticancer activity of camalexin, a major indole phytoalexin of Arabidopsis thaliana, against ovarian cancer stem cells. We demonstrate that camalexin inhibits proliferation and induces cell death in ovarian cancer stem cells that exhibit various molecular mechanisms of anticancer drug resistance. Furthermore, we present the mode of action of this prospective anticancer agent identified by combined approach that included in silico predictions, comprehensive analysis of whole-genome gene expression data and target-specific assays. Lastly, we demonstrate the relevance of the identified mode of action in context of ovarian cancer cell signaling. Citation Format: Roman Mezencev, John F. McDonald. Camalexin, an indole phytoalexin from Arabidopsis thaliana, displays activity against ovarian cancer stem cells. [abstract]. In: Proceedings of the 107th Annual Meeting of the American Association for Cancer Research; 2016 Apr 16-20; New Orleans, LA. Philadelphia (PA): AACR; Cancer Res 2016;76(14 Suppl):Abstract nr 1292.
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