Mechanism of Arsenic Trioxide on Apoptosis and Autophagy in Triple-negative Breast Cancer Stem Cell MDA-MB-231 Cell Line
Objective:To investigate the mechanism of arsenic trioxide on apoptosis and autophagy in triple negative breast cancer(TNBC)stem cell MDA-MB-231 cell line.Methods:The stem cells cultured in the second generation were taken for 5 and divided into four groups:control group,arsenic trioxide acting group,Rapa combined with arsenic trioxide group and 3-MA combined with arsenic trioxide group.The apoptosis rate,autophagy and protein expression were observed.Results:For 48 h,the total apoptosis was 40%.When 3MA inhibited the autophagic activity,the apoptosis induced by arsenic trioxide decreased by about 50%,and Rapa promoted the arsenic trioxide induced apoptosis increased by about 50%.Compared with the control group,the intracellular fluorescence intensity was higher in arsenic trioxide,Rapa combined with arsenic trioxide,and 3-MA combined with arsenic trioxide.Bax,Beclin-1 and P62 protein expression were higher in 3-MA and arsenic trioxide group and Rapa group,and Bcl-2 protein expression was lower than the group and Rapa with arsenic trioxide group(P<0.05).Conclusion:Arsenic trioxide induced autophagy and cell apoptosis coexist in MDA-MB-231 stem cells and may be regulated by common genes.Arsenic trioxide induced autophagy can promote cell apoptosis.
Triple-negative breast cancerArsenic trioxideApoptosisAutophagy