Author/Authors :
Yuen-Nei Cheung، نويسنده , , Jenny and Chik-Ying Ong، نويسنده , , Rose and Suen، نويسنده , , Yick-Keung and Ooi، نويسنده , , Vincent and Nai-Ching Wong، نويسنده , , Henry and Chung-Wai Mak، نويسنده , , Thomas and Fung، نويسنده , , Kwok-Pui and Yu، نويسنده , , Biao and Kong، نويسنده , , Siu Kai Kong، نويسنده ,
Abstract :
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 (ΔΨm), generation of H2O2, 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.
Keywords :
Polyphyllin D , Drug resistance , HepG2 , apoptosis