The Effect of Combining bcr-abl Antisense Phosphorothioate Oligodeoynucleotides and c-myb Aspo on K562 Cell Line
- VernacularTitle:联合应用bcr-abl融合基因反义寡核苷酸与c-myb基因反义寡核苷酸对K562细胞作用的研究
- Author:
Qizhen SHI
;
Lianhuang LU
- Publication Type:Journal Article
- Keywords:
antisense oligonucleotides;
bcr-abl;
c-myb;
K562 cell line
- From:
Chinese Journal of Cancer Biotherapy
2000;7(4):251-254
- CountryChina
- Language:Chinese
-
Abstract:
Objective: To study the effect of combining bcr-abl Aspo and c-myb Aspo on K562 cells. Methods: Cellswere exposed to oligomers. Cell inhibitory rate was determined by typan blue dye exclusion. CFU-K562 cells were culturedin 0.8% methyleellulose. P210 was measured by flow cytometry. Cellular bcr-abl mRNA was detected by RT-PCR semiquantitative analysis. Cell apoptosis was measured by flow cytometry and observed by electron microscope. Results: When the concentration of both bcr-abl Aspo and c-myb Aspo was 5 μmol/L, K562 cells were still growth in clone state. The growth inhibitory rate was 61.7% at 120 h. P210 was depressed at 24 h and went up to 25.7% at 120 h. The apoptosis rate was 22.5%. While K562 cells were dealt with 10 μmol/L bcr-abl Aspo and 10 μmol/L c-myb Aspo, the cells were growth in dispersal. The cell growth inhibitory rate reached to 92.2% and 64.3% of K562 cells were induced to apoptosisat 120 h. P210 was complelely depressed untill 120 h. The decrease of bcr-abl mRNA was from 69.2% to 85.3% after incubation 48 h with 5 μmol/L Aspo and 10 mol/L. Conclusion: It emerges coordination to combine bcr-abl Aspo and c-myb Aspo on K562 cells, and enhances the anti-leukemia effect.
