| Literature DB >> 26961871 |
Vittorio Caropreso1, Emad Darvishi1, Thomas J Turbyville2, Ranjala Ratnayake1, Patrick J Grohar3, James B McMahon1, Girma M Woldemichael4.
Abstract
High-throughput screening of extracts from plants, marine, and micro-organisms led to the identification of the extract from the plant Phyllanthus engleri as the most potent inhibitor of EWS-FLI1 induced luciferase reporter expression. Testing of compounds isolated from this extract in turn led to the identification of Englerin A (EA) as the active constituent of the extract. EA induced both necrosis and apoptosis in Ewing cells subsequent to a G2M accumulation of cells in the cell cycle. It also impacted clonogenic survival and anchorage-independent proliferation while also decreasing the proportion of chemotherapy-resistant cells identified by high ALDH activity. EA also caused a sustained increase in cytosolic calcium levels. EA appears to exert its effect on Ewing cells through a decrease in phosphorylation of EWS-FLI1 and its ability to bind DNA. This effect is mediated, at least in part, through a decrease in the levels of the calcium-dependent protein kinase PKC-βI after a transient up-regulation.Entities:
Keywords: DNA-binding protein; EWS-FLI1; Englerin A; Ewings sarcoma; calcium; inhibition mechanism; inhibitor; transcription factor
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Year: 2016 PMID: 26961871 PMCID: PMC4858959 DOI: 10.1074/jbc.M115.701375
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157