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Deprecated: Implicit conversion from float 243.2 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Oncotarget 2016 ; 7 (15): 20395-409 Nephropedia Template TP
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CWP232228 targets liver cancer stem cells through Wnt/?-catenin signaling: a novel therapeutic approach for liver cancer treatment #MMPMID26967248
Kim JY; Lee HY; Park KK; Choi YK; Nam JS; Hong IS
Oncotarget 2016[Apr]; 7 (15): 20395-409 PMID26967248show ga
Liver cancer stem cells (CSCs) are resistant to conventional chemotherapy and radiation, which may destroy tumor masses, but not all liver CSCs contribute to tumor initiation, metastasis, and relapse. In the present study, we showed that liver CSCs with elevated Wnt/?-catenin signaling possess much greater self-renewal and clonogenic potential. We further documented that the increased clonogenic potential of liver CSCs is highly associated with changes in Wnt/?-catenin signaling and that Wnt/?-catenin signaling activity is positively correlated with CD133 expression and aldehyde dehydrogenase (ALDH) enzymatic activity. Notably, the small molecule inhibitor CWP232228, which antagonizes the binding of ?-catenin to TCF in the nucleus, inhibits Wnt/?-catenin signaling and depletes CD133+/ALDH+ liver CSCs, thus ultimately diminishing the self-renewal capacity of CSCs and decreasing tumorigenicity in vitro and in vivo. Taken together, our findings suggest that CWP232228 acts as a candidate therapeutic agent for liver cancer by preferentially targeting liver CSCs.