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CWP232228 targets liver cancer stem cells through Wnt/?-catenin signaling: a novel therapeutic approach for liver cancer treatment.


ABSTRACT: 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.

SUBMITTER: Kim JY 

PROVIDER: S-EPMC4991463 | biostudies-literature | 2016 Apr

REPOSITORIES: biostudies-literature

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CWP232228 targets liver cancer stem cells through Wnt/β-catenin signaling: a novel therapeutic approach for liver cancer treatment.

Kim Ji-Young JY   Lee Hwa-Yong HY   Park Kwan-Kyu KK   Choi Yang-Kyu YK   Nam Jeong-Seok JS   Hong In-Sun IS  

Oncotarget 20160401 15


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/β-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/β-catenin signaling and that Wnt/β-c  ...[more]

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