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Abstract Objective To evaluate the anti-tumor activity and possible mechanism(s) of Platycodin D (PD), a major saponin
derived from Platycodin grandi?orum, in human prostate cancer cell lines. Methods Human prostate cancer cell lines (PC3, DU145
and LNCaP cells), and the non-malignant human prostate epithelial cell line, RWPE-1, were exposed to various concentrations of PD
to evaluate its cytotoxicity in vitro (via the MTT assay). Cell cycle analysis was indicated by PI staining with ?ow cytometry. Cell
cycle-related proteins levels were assessed by Western blotting. Results PD exerted cytotoxicity against three prostate cancer cell
lines, PC3 cells, DU145 cells, and LNCaP cells, with half-maximal inhibitory concentrations (IC50) in the range of 11.17 to 26.13
μmol/L. The PC3 cells were the most sensitive to PD. After being treated with PD for 48 hours, the PC3 cells were arrested in the G2/
M phase, and the DU145 and LNCaP cells were arrested in the G0 /G1 phase. Western blotting analysis indicated that PD exposure
decreased the levels of cell cycle-related proteins, including E2F1, CDK2, CDK4, CDK6, CyclinD1, Cdc2, CyclinB1. Conclusions
PD exhibits signifcant inhibitory activities against prostate cancer cells, which provides a basis for future development of human
prostate cancer chemotherapy.
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| [1] |
1ZHU He-cheng, 1YANG Sheng, 2ZHU Bin, 1XU Yang, 1YAO Yi, 1LI Wang, 1TANG Da-han, 1HUANG Ya-jing, 1LUO Yi, 2REN Cai-ping . Antitumor experimental study on compound of phytochemicals[J]. Electronic Journal of Metabolism and Nutrition of, 2019, 6(1): 47-52. |
| [2] |
. Dietary fiber and prostate cancer risk[J]. Electronic Journal of Metabolism and Nutrition of, 2016, 3(1): 63-65. |
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2015, Vol. 2 
