Title :
Induction of Apoptosis in HepG2 Cells by Solanine
Author :
Gao, Shiyong ; Ji, Yubin ; Ji, Chenfeng ; Zou, Xiang
Author_Institution :
Center for Life Sci. & Environ. Sci., Harbin Commerce Univ., Harbin, China
Abstract :
The nightshade (Solanum nigrum Linn.) has been widely used in Chinese traditional medicine as a remedy for the treatment of digestive system cancer. The anti-tumor activity of solanine, a steroid alkaloid isolated from the nightshade has been demonstrated. To observe the effect of antitumor and mechanism of solanine. The MTT assay was used to evaluate the IC50 on the 3 digestive system tumor cell lines; The effect on the morphology was observed with a laser confocal microscopy; The rate of apoptosis and the cell cycle were measured using flow cytometry. The results show the IC50 for HepG2, SGC-7901, and LS-174 were 14.47, >50, and >50 mug/ml, respectively; The morphology of cells in the negative control was normal; For the treated groups, typical signs for apoptosis were found. The rate of apoptosis in HepG2 cells induced by solanine was found to be 6.0%, 14.4%, 17.3%, 18.9%, and 32.2%, respectively. Observation of the cell cycle showed that cells in the G2/M phases disappeared while the number of cells in the S phase increased significantly for treated groups. Therefore, the solanine could induce apoptosis in HepG2 cells.
Keywords :
biomedical measurement; biomedical optical imaging; cancer; cellular biophysics; drugs; laser applications in medicine; optical microscopy; patient treatment; tumours; Chinese traditional medicine; HepG2 cells; MTT assay; Solanum nigrum Linn; antitumor activity; apoptosis; cell cycle measurement; cell morphology; digestive system cancer treatment; flow cytometry; laser confocal microscopy; nightshade; solanine; steroid alkaloid; Bovine; Business; Cancer; Cells (biology); Digestive system; Drugs; Humans; Morphology; Pancreas; Tumors;
Conference_Titel :
Bioinformatics and Biomedical Engineering , 2009. ICBBE 2009. 3rd International Conference on
Conference_Location :
Beijing
Print_ISBN :
978-1-4244-2901-1
Electronic_ISBN :
978-1-4244-2902-8
DOI :
10.1109/ICBBE.2009.5162948