| Literature DB >> 24863036 |
Jiawei Liu1, Qing Zhang2, Yushan Ye3, Wuguo Li3, Junxin Qiu3, Jingli Liu2, Ruoting Zhan3, Weiwen Chen3, Qiang Yu2.
Abstract
STAT3 signaling pathway is an important target for human cancer therapy. Thus, the identification of small-molecules that target STAT3 signaling will be of great interests in the development of anticancer agents. The aim of this study was to identify novel inhibitors of STAT3 pathway from the roots of Zanthoxylum nitidum (Roxb.) DC. The bioassay-guided fractionation of MeOH extract of Z. nitidum using a STAT3-responsive gene reporter assay led to the isolation of angoline (1) as a potent and selective inhibitor of the STAT3 signaling pathway (IC50=11.56 μM). Angoline inhibited STAT3 phosphorylation and its target gene expression and consequently induced growth inhibition of human cancer cells with constitutively activated STAT3 (IC50=3.14-4.72 μM). This work provided a novel lead for the development of anti-cancer agents targeting the STAT3 signaling pathway.Entities:
Keywords: Angoline; Inhibitor; STAT3 signaling pathway; Zanthoxylum nitidum
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Year: 2014 PMID: 24863036 DOI: 10.1016/j.phymed.2014.04.001
Source DB: PubMed Journal: Phytomedicine ISSN: 0944-7113 Impact factor: 5.340