Bortezomib-induced BiP expression and apoptosis in multiple myeloma cells.
- Author:
Hong-Juan DONG
1
;
Xie-Qun CHEN
;
Guang-Xun GAO
;
Hong-Tao GU
;
Yao-Zhu PAN
;
Ying GAO
;
Hua-Feng ZHU
Author Information
1. Department of Hematology, The Fourth Military Medical University, Xi'an 710032, China.
- Publication Type:Journal Article
- MeSH:
Apoptosis;
drug effects;
Boronic Acids;
pharmacology;
Bortezomib;
Cell Line, Tumor;
Endoplasmic Reticulum;
drug effects;
metabolism;
Heat-Shock Proteins;
metabolism;
Humans;
Multiple Myeloma;
metabolism;
pathology;
Pyrazines;
pharmacology;
RNA, Messenger;
genetics
- From:
Journal of Experimental Hematology
2009;17(1):107-110
- CountryChina
- Language:Chinese
-
Abstract:
This study was aimed to explore the effect of bortezomib on the apoptosis and expression of the molecular chaperone BiP in human multiple myeloma cell line NCI-H929 (H929). After treatment of H929 cells with different concentrations of bortezomib for 24 hours, cell apoptosis was assayed by flow cytometry with Annexin V-FITC/PI staining, and the expression levels of BiP mRNA and protein were detected by RT-PCR and Western blotting analysis. The results showed that bortezomib of different concentrations (20, 40 and 80 nmol/L) induced apoptosis of H929 cells in dose-dependent manner, with apoptotic rates (15.73 +/- 0.67)%, (27.83 +/- 1.26)% and (44.17 +/- 2.25)% respectively, which were significantly higher than that in control (1.21 +/- 0.07%) (p < 0.05). Bortezomib-induced up-regulation of BiP mRNA levels was almost on a parallel with BiP protein when compared with control. Under the similar apoptosis-stimulating conditions with apoptotic rates varying from 40% to 50%, expression levels of BiP mRNA and BiP protein induced by the classical endoplasmic reticulum stressor Brefeldin A (500 ng/ml, 24 h) were almost consistent with those by bortezomib (80 nmol/L, 24 h). It is concluded that bortezomib-induced apoptosis in H929 cells correlates closely with endoplasmic reticulum stress.
