The enhancing effect of curcumin on the sensitivity of cisplatin-resistance human ovarian cancer cell line COC1/DDP to cisplatin
Dai Ji
Abstract
Dai Ji
Abstract
Objective To investigate the association of curcumin use with the sensitivity of cisplatin-resistant ovarian cancer line COC1/DDP to cisplatin.Methods The effects of curcumin alone,cisplatin alone,or a combined therapy with both agents on the proliferation and apoptosis in cisplatin-resistant cells COC1/DDP were determined by MTT assay and TUNEL.The expressions of apoptosis-associated genes Bcl-2 and Smac were detected using RT-PCR.Results Coadministration of cisplatin at concentrations of 1.25 to 5 μg/mL with curcumin markedly decreased the survival rate of COC1/DDP(P0.05);and the most significant deline in the rate occurred after the use of 2.5 μg/mL of cisplatin combined with 20 μmol/L of curcumin.As compared with cisplatin or curcumin alone,the combination therapy evidently increased the apoptotic rate,downregulated the expression of Bcl-2 mRNA,and upregulated that of Smac mRNA(P0.05 for all comparisons).Conclusions Curcumin can inhibit the growth of COC1/DDP and enhance the sensitivity of the cells to cisplatin,whose mechanism may be associated with the upregulation of Smac and downregulation of Bcl-2.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective To investigate the association of curcumin use with the sensitivity of cisplatin-resistant ovarian cancer line COC1/DDP to cisplatin.Methods The effects of curcumin alone,cisplatin alone,or a combined therapy with both agents on the proliferation and apoptosis in cisplatin-resistant cells COC1/DDP were determined by MTT assay and TUNEL.The expressions of apoptosis-associated genes Bcl-2 and Smac were detected using RT-PCR.Results Coadministration of cisplatin at concentrations of 1.25 to 5 μg/mL with curcumin markedly decreased the survival rate of COC1/DDP(P0.05);and the most significant deline in the rate occurred after the use of 2.5 μg/mL of cisplatin combined with 20 μmol/L of curcumin.As compared with cisplatin or curcumin alone,the combination therapy evidently increased the apoptotic rate,downregulated the expression of Bcl-2 mRNA,and upregulated that of Smac mRNA(P0.05 for all comparisons).Conclusions Curcumin can inhibit the growth of COC1/DDP and enhance the sensitivity of the cells to cisplatin,whose mechanism may be associated with the upregulation of Smac and downregulation of Bcl-2.
Key concepts: Cisplatin, Curcumin, Downregulation and upregulation, Apoptosis, Ovarian cancer, MTT assay, TUNEL assay, Chemistry