Xia Ding1, Fang-Shi Zhu, Min Li, Si-Guo Gao. 1. Department of Chemistry, College of Science, Nanjing Agricutural University, Nanjing, PR China. dingxia@njau.edu.cn
Abstract
ETHNOPHARMACOLOGICAL RELEVANCE: Solanum nigrum L. (SNL), a traditional Chinese medicinal herb endowed with diuretic, antipyretic and hepatoprotective effects, has been used as a major ingredient of folk prescriptions for anticancer treatment in China. AIM OF THE STUDY: The purpose of this study was to evaluate the inhibitory effect of solamargine (SM), a major steroidal alkaloid glycoside purified from SNL, on human hepatoma SMMC-7721 cells and investigate the possible mechanism of SM. MATERIALS AND METHODS: The MTT assay was used to evaluate the IC(50) on tumor cell lines. The effect on morphology was observed with a light or fluorescence microscopy. The rate of apoptosis and the cell cycle were measured using flow cytometry (FCM). The expression of caspase-3 protein was measured by colorimetric assay. RESULTS: SM significantly inhibited the growth of SMMC-7721 and HepG2 cells and induced cell apoptosis. Cell cycle analysis revealed that SM caused cell cycle arrest at the G2/M phase. Moreover, SM could up-regulate the expression of caspase-3. CONCLUSIONS: This study indicated that SM exerted potential anticancer activity on SMMC-7721 cells in vitro through the activation of caspase-3 and the regulation of the cell cycle progression to induce apoptosis and inhibit hepatoma cells proliferation.
ETHNOPHARMACOLOGICAL RELEVANCE: Solanum nigrum L. (SNL), a traditional Chinese medicinal herb endowed with diuretic, antipyretic and hepatoprotective effects, has been used as a major ingredient of folk prescriptions for anticancer treatment in China. AIM OF THE STUDY: The purpose of this study was to evaluate the inhibitory effect of solamargine (SM), a major steroidal alkaloidglycoside purified from SNL, on humanhepatomaSMMC-7721 cells and investigate the possible mechanism of SM. MATERIALS AND METHODS: The MTT assay was used to evaluate the IC(50) on tumor cell lines. The effect on morphology was observed with a light or fluorescence microscopy. The rate of apoptosis and the cell cycle were measured using flow cytometry (FCM). The expression of caspase-3 protein was measured by colorimetric assay. RESULTS:SM significantly inhibited the growth of SMMC-7721 and HepG2 cells and induced cell apoptosis. Cell cycle analysis revealed that SM caused cell cycle arrest at the G2/M phase. Moreover, SM could up-regulate the expression of caspase-3. CONCLUSIONS: This study indicated that SM exerted potential anticancer activity on SMMC-7721 cells in vitro through the activation of caspase-3 and the regulation of the cell cycle progression to induce apoptosis and inhibit hepatoma cells proliferation.