Chemical composition of total flavonoids from Salvia chinensia Benth and their pro-apoptotic effect on hepatocellular carcinoma cells: Potential roles of suppressing cellular NF-κB signaling

•TSFC induces HCC cell apoptosis in vitro and in vivo.•TSFC suppresses NF-κB activity in HCC cells.•TSFC exhibits low toxic effects to tumor-bearing mice. Salvia chinensia Benth (S. chinensia) is a medical plant that has been traditionally applied for centuries in the treatment of malignant diseases...

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Veröffentlicht in:Food and chemical toxicology 2013-12, Vol.62, p.420-426
Hauptverfasser: Xiang, Meixian, Su, Hanwen, Hu, Yajing, Hu, Yun, Yang, Tianming, Shu, Guangwen
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Sprache:eng
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Zusammenfassung:•TSFC induces HCC cell apoptosis in vitro and in vivo.•TSFC suppresses NF-κB activity in HCC cells.•TSFC exhibits low toxic effects to tumor-bearing mice. Salvia chinensia Benth (S. chinensia) is a medical plant that has been traditionally applied for centuries in the treatment of malignant diseases including hepatocellular carcinoma (HCC). However, the scientific basis underlying its anti-HCC activity has not been fully established. In this study, the chemical profiles of total flavonoids from S. chinensia (TFSC) were explored. Thirteen compounds which constituted the major components of TFSC were separated and identified. Flow cytometry analysis and caspase activity assays showed that TFSC dose-dependently induced HepG2 and Huh-7 HCC cell apoptosis. TFSC was also shown to substantially suppress NF-κB activity in HCC cells. Moreover, TFSC significantly repressed transplanted murine H22 ascitic hepatic cancer cell growth in vivo. Further studies revealed that TFSC induced HCC cell apoptosis and inhibited expressional levels of NF-κB responsive genes in transplanted tumor tissues. In addition, the toxic impact of TFSC on tumor-bearing mice was undetectable. These results indicate that TFSC induces HCC cell apoptosis both in vitro and in vivo. The suppression of cellular NF-κB activity is implicated in the TFSC-mediated HCC cell apoptosis.
ISSN:0278-6915
1873-6351
DOI:10.1016/j.fct.2013.09.008