Effects of doxorubicin on the expressions of BRCA1 and PARP-1 proteins in breast cancer MCF-7 cells / 肿瘤
Tumor
; (12): 385-391, 2013.
Article
em Zh
| WPRIM
| ID: wpr-848995
Biblioteca responsável:
WPRO
ABSTRACT
Objective: To investigate the effects of doxorubicin on the expressions of DNA-damage/repair-related proteins BRCA1 (breast cancer-associated protein 1) and PARP-1 [poly(ADP-ribose) polymerase-1] in BRCA1 wild-type breast cancer MCF-7 cells. Methods: The MCF-7 cells were treated with doxorubicin, then the expressions of BRCA1 and PARP-1 and the activity of PARP-1 in the cells recovering after different time peroids were detected by Western blotting. The apoptotic rates of MCF-7 cells and SKBR3.0 cells (BRCA1 mutant-type breast cancer cells) after intervention with doxorubicin and PARP-1 inhibitor 3-ABA (3-aminobenzamide) were detected by FCM (flow cytometry). Results: After MCF-7 cells were treated with different concentrations of doxorubicin for 24 h and then recovered for 12 h, the expression of PAR [poly(ADP-ribose)], an active product of PARP-1, was increased in a dose-dependent manner (P 0.05). Both doxorubicin and 3-ABA alone could significantly induce the apoptosis of MCF-7 cells (P < 0.05), and the combination of the two could further increase the apoptosis of BRCA1 wild-type breast MCF-7 cells (P < 0.05). Doxorubicin in combination with 3-ABA could also induce the apoptosis of BRCA1 mutant-type SKBR3.0 cells, and this effect was stronger than that in MCF-7 cells (P < 0.05). Conclusion: Doxorubicin intervention can affect the activity of DNA-damage/repair-related protein PARP-1 and the expression of BRCA1. Both doxorubicin and PARP-1 inhibitor 3-ABA can induce the apoptosis of MCF-7 cells, and the combination of the two can increase this apoptosis-inducing effect. Copyright © 2013 by TUMOR.
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WPRIM
Idioma:
Zh
Revista:
Tumor
Ano de publicação:
2013
Tipo de documento:
Article