Relation of apoptosis of K562 cells induced by naringenin in vitro to enzyme activity changes of caspase-3 and caspase-8 and expression of FAS/FASL proteins.
- Author:
Xue-Lan ZUO
1
;
Ying ZHOU
;
Rui-Fang LI
;
Ying-Qian FENG
;
Li HE
;
Ming-Hui LIU
Author Information
1. Department of Hematology, Zhongnan Hospital, Wuhan University, Wuhan 430071, Hubei Province, China. zuoxuelan2004@126.com
- Publication Type:Journal Article
- MeSH:
Antineoplastic Agents, Phytogenic;
pharmacology;
Apoptosis;
drug effects;
Caspase 3;
metabolism;
Caspase 8;
metabolism;
Fas Ligand Protein;
genetics;
metabolism;
Flavanones;
pharmacology;
Humans;
K562 Cells;
fas Receptor;
genetics;
metabolism
- From:
Journal of Experimental Hematology
2008;16(2):286-289
- CountryChina
- Language:Chinese
-
Abstract:
The objective of this study was to investigate the apoptosis-inducing effect and underlying mechanism of naringenin (NGEN) on K562 cells in vitro. The inhibition of NGEN on K562 cells was evaluated by means of MTT assay so as to observe the cytotoxicity of NGEN; The morphological changes of the cells treated by NGEN were observed by transmission electron microscope; cell apoptosis rate influenced by NGEN was assessed by flow cytometry; the enzyme activity changes of caspase-3 and caspase-8 in the process of NGEN-induced K562 apoptosis were detected by Caspase Colorimetric Assay Kit; immunohistochemistry technique was used to detect FAS, FASL protein expression in K562 cells. The results showed that the growth of cells was inhibited by NGEN in dose-and time-dependent manners (p<0.05); NGEN-induced K562 cells apoptosis and sub-G1 peak was observed; some typically early and final phase changes of cell apoptosis were revealed under transmission electron microscope; the enzyme activity of caspase-3 and caspase-8 and the expression of FAS remarkably increased, meanwhile the expression of FASL was down-regulated (p<0.05). It is concluded that NGEN exerts anti-cancer effect by inducing K562 cell apoptosis, and the regulation of the expression of FAS and FASL. The caspase-3 and caspase-8 co-pathway brings about one of the mechanisms.
