Induction of Apoptosis in Human Promyelocytic Leukemia HL60 Cells by Panaxynol and Panaxydol

被引:28
|
作者
Yan, Zhonghong [1 ]
Yang, Ruolin [1 ]
Jiang, Yi [2 ]
Yang, Zhihui [3 ]
Yang, Junrui [2 ]
Zhao, Qian [2 ]
Lu, Yang [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Dept Pharm, Shanghai 200025, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Med, Dept Pathophysiol, Shanghai 200025, Peoples R China
[3] Louisiana State Univ, Hlth Sci Ctr, Ctr Neurosci Excellence, New Orleans, LA 70112 USA
关键词
panaxynol; panaxydol; apoptosis; promyelocytic leukemia cell; KINASE-C-DELTA; FLOW-CYTOMETRY; GINSENG; POLYACETYLENES; PROLIFERATION; VEGETABLES; ETOPOSIDE;
D O I
10.3390/molecules16075561
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Panaxynol and panaxydol are naturally occurring polyacetylenes, isolated from the lipophilic fractions of Panax notoginseng, that exert anti-proliferative effects against malignant cells. However, to the best of our knowledge, no study concerning the inhibitory effects of the two polyacetylenes on cell growth of human promyelocytic leukemia cells has been reported. In this paper, we examined the antiproliferation and proapoptotic effects of panaxynol and panaxydol on HL60 cells and investigated their mechanism of action. Cell growth inhibition of panaxynol and panaxydol were determined by trypan blue dye exclusion assays. Apoptosis of cells was revealed by morphological observation, analysis for nuclear DNA distribution and by annexin V-FITC/PI staining using flow cytometry. It was found that panaxynol and panaxydol markedly inhibited proliferation of HL60 cells in a time-and dose-dependent manner via an apoptotic pathway. In concern with these findings, Western blot analysis showed proteolytic activation of PKC delta, caspase-3 activation and cleavage of poly (ADP [adenosine diphosphate]-ribose) polymerase in HL60 cells treated by panaxynol and panaxydol. In conclusion, panaxynol and panaxydol have profound effects on growth and apoptosis of HL60 cells, suggesting those substances are worthy of further exploration as potential anti-cancer agents.
引用
收藏
页码:5561 / 5573
页数:13
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