Effects of TIEG1 on K562 cell apoptosis and expression of BCL-2/BAX, PTEN.
10.7534/j.issn.1009-2137.2014.05.017
- Author:
Kun YAO
1
;
Hai-Xia ZHU
1
;
Rong ZHANG
1
;
Ai-Jun LIAO
1
;
Wei YANG
1
;
Zhuo-Gang LIU
2
Author Information
1. Hematology Center of China Medical University Shengjing Hospital, Shengyang 100021, Liaoning Province, China.
2. Hematology Center of China Medical University Shengjing Hospital, Shengyang 100021, Liaoning Province, China. E-mail: liuzg2h@sina.com.
- Publication Type:Journal Article
- MeSH:
Apoptosis;
Cell Proliferation;
Humans;
K562 Cells;
Kruppel-Like Transcription Factors;
metabolism;
PTEN Phosphohydrolase;
metabolism;
Proto-Oncogene Proteins c-bcl-2;
metabolism;
bcl-2-Associated X Protein;
metabolism
- From:
Journal of Experimental Hematology
2014;22(5):1278-1281
- CountryChina
- Language:Chinese
-
Abstract:
The aim of this study was to investigate the effect of TIEG1 on K562 cell apoptosis and expression of BCL-2/BAX, PTEN. The different concentration(0, 1, 5, 10, 20 ng/ml) of TIEG1 were used to treat K562 cells, the cell growth inhibition rate was detected by using MTT method. After treating K562 cells with 10.00 ng/ml TIEG1, the cell apoptosis was detected with flow cytometry. The RT-PCR was used to detected the expression levels of BCL-2 /BAX and PTEN. The results showed that TIEG1 displays inhibitory effect on proliferation of K562 cells in time-and dose-dependent manner (r = 0.52, P < 0.05) ; after K562 cells were treated for 6, 12, 24 and 48 h, the IC50 of TIEG1 were 48.19, 18.72, 9.5 and 3.85 ng/ml respectively. After treating K562 cells with 10.00 ng/ml TIEG1 for 0, 6, 12, 24, 48 h, the apoptosis rate were (2.13 ± 0.42)%, (7.79 ± 0.71)%, (11.17 ± 1.37)%, (24.66 ± 0.29)% and (48.60 ± 1.38)% respectively, and there was significant difference between groups(P < 0.05). In process of K562 cell apoptosis, the expression level of BCL-2 gradually decreased (r = 0.48, P < 0.05), meanwhile the expression levels of BAX (r = 0.69, P < 0.05) and PTEN (r = 0.57, P < 0.05) gradually increased. It is concluded that TIEG1 can indue apoptosis of K562 cells and inhibit K562 cell proliferation in time-and dose-dependent manner. In apoptosis process of K562 cells induced by TIEG1, the expression changes of BCL-2/BAX and PTEN associate with the K562 cell apoptosis.
