Title : Inhibiting inducible miR-223 further reduces viable cells in human cancer cell lines MCF-7 and PC3 treated by celastrol.

Pub. Date : 2015 Nov 9

PMID : 26552919






4 Functional Relationships(s)
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1 Celastrol"s miR-223 induction might be due to NF-kappaB inhibition and transient mTOR activation: these two events occurred prior to miR-223 elevation in celastrol-treated cells. celastrol mechanistic target of rapamycin kinase Homo sapiens
2 NF-kappaB inhibitor, like celastrol, could induce miR-223; the induction of miR-223 by NF-kappaB inhibitor or celastrol was reduced by the use of mTOR inhibitor. celastrol mechanistic target of rapamycin kinase Homo sapiens
3 NF-kappaB inhibitor, like celastrol, could induce miR-223; the induction of miR-223 by NF-kappaB inhibitor or celastrol was reduced by the use of mTOR inhibitor. celastrol mechanistic target of rapamycin kinase Homo sapiens
4 Finally and interestingly, miR-223 also could affect NF-kappaB and mTOR and the effects were different between cells treated or not treated with celastrol, thus providing an explanation for differing effects of miR-223 alteration on cellular viability in the presence of celastrol or not. celastrol mechanistic target of rapamycin kinase Homo sapiens