| Literature DB >> 29974605 |
I-Lun Hsin1,2, Jen-Chieh Hsu1, Wen-Jun Wu1, Hsueh-Ju Lu3,4, Ming-Fang Wu1,3,4,5, Jiunn-Liang Ko1,3,4.
Abstract
β-catenin is important in development of lung cancer. In our previous study, GMI, a fungal immunomodulatory protein, inhibits lung cancer cell survival. The aim of this study is to evaluate the effect of GMI on β-catenin inhibition and apoptosis induction. GMI induced apoptosis in lung cancer cells bearing wild-type and mutated EGFR. GMI did not reduce the β-catenin mRNA expression but suppressed the protein expressions of β-catenin that resulted in the transcriptional downregulation of its target genes: survivin and cyclin-D1. The transcriptional activation activity of β-catenin was demonstrated by TOPFLASH/FOPFLASH luciferase reporter assay. Inhibition of GSK-3β and proteasome blocked the inhibiting effect of GMI on β-catenin and its target genes. β-catenin silencing increased activation of apoptosis in GMI-treated H1355 cells. This is the first study to reveal the novel function of GMI in inducing apoptosis via β-catenin inhibition. These results provide a new potential of GMI in against lung cancer.Entities:
Keywords: GMI; apoptosis; fungal immunomodulatory protein; lung cancer; β-catenin
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Year: 2018 PMID: 29974605 DOI: 10.1002/tox.22582
Source DB: PubMed Journal: Environ Toxicol ISSN: 1520-4081 Impact factor: 4.119