Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/50324
Title: Pure curcumin inhibits exogenous Wilms' tumor (WT1) (+/+) isoform protein via degradation pathway and protein kinase C in transfected U937 cells
Authors: Suwanna Semsri
Songyot Anuchapreeda
Nujeera Intasai
Tanyarat Jomgeow
Singkome Tima
Colleen Sweeney
Pornngarm Limtrakul
Keywords: Pharmacology, Toxicology and Pharmaceutics
Issue Date: 29-Oct-2011
Abstract: Wilms' tumor (WT1) gene overexpresses in leukemic cells which is alternatively spliced at two sites, yielding four isoforms: WT1 (+/+), (+/-), (-/+), and (-/-). Curcumin is one of major active components of the spice turmeric, widely known as anticancer. This study investigated the effects and inhibitory mechanism of pure curcumin on WT1 isoform-transfected U937 cells. WT1 transfected U937 cells were initially treated for 24 h, with 10 μM pure curcumin. Pure curcumin exhibited a strong inhibitory effect on WT1 (+/+) mRNA level detected by real time PCR. Treatment of WT1 transfected U937 cells with non-cytotoxic doses (10, 15, and 17 μM) of pure curcumin decreased WT1 protein levels in a dose dependent manner. Pure curcumin at the concentration of 15 μM significantly decreased the protein levels of the WT (+/+) isoform in a time-dependent manner. It also decreased exogenous WT1 (+/+) protein half-life. WT1 protein expression was inhibited by protein kinase C inhibitor (GF109203x) suggesting that pure curcumin decreased exogenous WT1 (+/+) expression in transfected U937 cells via protein kinase C during post-translational processing. ©2011 Academic Journals.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=80655146486&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/50324
ISSN: 19960816
Appears in Collections:CMUL: Journal Articles

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