The effect of apoptosis induction by proteasom inhibitor MG132 combined with cisplatin in lung adenocarcinoma cell line A549
Yujie Han, Song Zhao, Yang Yang, Donglei Liu, Kai Wu
Abstract
Yujie Han, Song Zhao, Yang Yang, Donglei Liu, Kai Wu
Abstract
Objective To observe the change of the expression of the apoptosis-related factor Caspase-9 and nuclear factor-κB (NF-<B) of proteasome inhibitor MG132 combined with cisplatin (DDP) on lung adneocarinoma cell line A549.Methods Inhibition rates of the lung adenocarcinoma cell line A549 intervened by 30 μmol/L MG132 and/or 20 mg/L DDP were tested by cell counting Kit-8 (CCK-8).The morphological changes of cells were detected by Hochest33342 staining.The cells apoptosis rates were examined by flow cytometry.The changes of expression of the apoptosis-related factors Caspase-9 and NF-κB were measured by Western blotting analysis.Results CCK-8 showed that the MG132 or DDP can effectively inhibit the proliferation of cells in a dose and time-dependent manner.The flow cytometry (FCM) showed that the apoptosis rate of cells treated with MG132 and DDP (65.43 ± 1.09)% was obviously increased than that alonely treated with MG132 (23.23 ± 0.96)% or DDP (24.86 ± 0.40)%.Compared with the group treated MG132 or DDP,The expression of the apoptosis-related factor Caspase-9 of the combining group was significantly up-regulated and the expression of NF-κB wa significantly decreased.Conclusion MG132 combined with DDP can apparently increased the apoptosis rate of lung adneocarinoma cell line A549 through decreasing the expression of NF-κB and enhancing the expression of Caspase-9. Key words: Lung adenocarcinoma cell line A549; MG132; Cisplatin; Nuclear factor-kappa B
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Objective To observe the change of the expression of the apoptosis-related factor Caspase-9 and nuclear factor-κB (NF-<B) of proteasome inhibitor MG132 combined with cisplatin (DDP) on lung adneocarinoma cell line A549.Methods Inhibition rates of the lung adenocarcinoma cell line A549 intervened by 30 μmol/L MG132 and/or 20 mg/L DDP were tested by cell counting Kit-8 (CCK-8).The morphological changes of cells were detected by Hochest33342 staining.The cells apoptosis rates were examined by flow cytometry.The changes of expression of the apoptosis-related factors Caspase-9 and NF-κB were measured by Western blotting analysis.Results CCK-8 showed that the MG132 or DDP can effectively inhibit the proliferation of cells in a dose and time-dependent manner.The flow cytometry (FCM) showed that the apoptosis rate of cells treated with MG132 and DDP (65.43 ± 1.09)% was obviously increased than that alonely treated with MG132 (23.23 ± 0.96)% or DDP (24.86 ± 0.40)%.Compared with the group treated MG132 or DDP,The expression of the apoptosis-related factor Caspase-9 of the combining group was significantly up-regulated and the expression of NF-κB wa significantly decreased.Conclusion MG132 combined with DDP can apparently increased the apoptosis rate of lung adneocarinoma cell line A549 through decreasing the expression of NF-κB and enhancing the expression of Caspase-9. Key words: Lung adenocarcinoma cell line A549; MG132; Cisplatin; Nuclear factor-kappa B
Key concepts: MG132, Apoptosis, A549 cell, Flow cytometry, Cisplatin, Cell culture, Chemistry, Molecular biology