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10.3390/ijms18102025

http://scihub22266oqcxt.onion/10.3390/ijms18102025
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C5666707!5666707!28934130
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suck abstract from ncbi


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pmid28934130      Int+J+Mol+Sci 2017 ; 18 (10): ä
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  • Isoliquiritigenin Induces Autophagy and Inhibits Ovarian Cancer Cell Growth #MMPMID28934130
  • Chen HY; Huang TC; Shieh TM; Wu CH; Lin LC; Hsia SM
  • Int J Mol Sci 2017[Oct]; 18 (10): ä PMID28934130show ga
  • Ovarian cancer is one of the commonest gynecologic malignancies, which has a poor prognosis for patients at the advanced stage. Isoliquiritigenin (ISL), an active flavonoid component of the licorice plant, previously demonstrated antioxidant, anti-inflammatory, and tumor suppressive effects. In this study, we investigated the antitumor effect of ISL on human ovarian cancer in vitro using the human ovarian cancer cell lines, OVCAR5 and ES-2, as model systems. Our results show that ISL significantly inhibited the viability of cancer cells in a concentration- and time-dependent manner. Flow cytometry analysis indicated that ISL induced G2/M phase arrest. Furthermore, the expression of cleaved PARP, cleaved caspase-3, Bax/Bcl-2 ratio, LC3B-II, and Beclin-1 levels were increased in western blot analysis. To clarify the role of autophagy and apoptosis in the effect of ISL, we used the autophagy inhibitor?3-methyladenine (3-MA) to attenuate the punctate fluorescence staining pattern of the p62/sequestosome 1 (SQSTM1, red fluorescence) and LC3 (green fluorescence) proteins after ISL treatment, and 3-MA inhibited the cytotoxicity of ISL. These findings provide new information about the link between ISL-induced autophagy and apoptosis and suggest that ISL is a candidate agent for the treatment of human ovarian cancer.
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