Polyphyllin D is a potent apoptosis inducer in drug-resistant HepG2 cells

In a search for new anticancer agents, we identified a novel compound polyphyllin D (PD) (diosgenyl α- l-rhamnopyranosyl-(1→2)-(α- l-arabinofuranosyl)-(1→4)]-[β- d-glucopyranoside) that induced DNA fragmentation and phosphatidyl-serine (PS) externalization in a hepatocellular carcinoma cell line Hep...

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Veröffentlicht in:Cancer letters 2005-01, Vol.217 (2), p.203-211
Hauptverfasser: Yuen-Nei Cheung, Jenny, Chik-Ying Ong, Rose, Suen, Yick-Keung, Ooi, Vincent, Nai-Ching Wong, Henry, Chung-Wai Mak, Thomas, Fung, Kwok-Pui, Yu, Biao, Kong, Siu-Kai
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Sprache:eng
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Zusammenfassung:In a search for new anticancer agents, we identified a novel compound polyphyllin D (PD) (diosgenyl α- l-rhamnopyranosyl-(1→2)-(α- l-arabinofuranosyl)-(1→4)]-[β- d-glucopyranoside) that induced DNA fragmentation and phosphatidyl-serine (PS) externalization in a hepatocellular carcinoma cell line HepG2 derivative with drug resistance (R-HepG2). PD is a saponin originally found in a tradition Chinese medicinal herb Paris polyphylla. It has been used to treat liver cancer in China for many years. We evaluated the cell-killing mechanisms of this compound in R-HepG2 and its parental cells. The mitochondrial apoptotic pathway was found to be involved in the PD-induced apoptosis because PD elicited depolarization of mitochondrial transmembrane potential (Δ Ψm), generation of H 2O 2, as well as release of cytochrome c and apoptosis-inducing factor in a dose- and time-dependent manner. In conclusion, we show for the first time that PD is a potent anticancer agent that can overcome drug resistance in R-HepG2 cells and elicit programmed cell death via mitochondrial dysfunction.
ISSN:0304-3835
1872-7980
DOI:10.1016/j.canlet.2004.06.042