摘要Objective:The effects of arsenic trioxide(As2O3)on hepatocellular carcinoma have been documented widely.Autophagy plays dual roles in the survival and death of cancer cells.Therefore,we investigated the exact role of autophagy in As2O3-induced apoptosis in liver cancer cells.Methods:The viability of hepatoma cells was determined using the MTT assay with or without fetal bovine serum.The rate of apoptosis in liver cancer cells treated with As2O3 was evaluated using flow cytometry,Hoechst 33258 staining,and TUNEL assays.The rate of autophagy among liver cancer cells treated with As2O3 was detected using immunofluorescence,Western blot assay and transmission elec-tron microscopy.Results:Upon treatment with As2O3,the viability of HepG2 and SMMC-7721 cells was decreased in a time-and dose-dependent manner.The apoptosis rates of both liver cancer cell lines increased with the concentration of As2O3,as shown by flow cytometry.Apoptosis in liver cancer cells treated with As2O3 was also shown by the activation of the caspase cascade and the regulation of Bcl-2/Bax expression.Furthermore,As2O3 treatment induced autophagy in liver cancer cells;this finding was supported by Western blot,immunofluorescence of LC3-Ⅱ and beclin 1,and transmission electron microscopy.In liver cancer cells,As2O3 inhibited the phosphoinositide 3-kinase/protein kinase B/mammalian target of rapa-mycin(PI3K/AKT/mTOR)signal pathway that plays a vital role in both apoptosis and autophagy.The PI3K activator SC-79 partially reversed As2O3-induced autophagy and apoptosis.Furthermore,inhibiting autophagy with 3-methyladenine partially reversed the negative effects of As2O3 on cell viability.Serum starvation increased autophagy and amplified the effect of As2O3 on cell death.Conclusion:As2O3 induces apoptosis and autophagy in liver cancer cells.Autophagy induced by As2O3 may have a proapoptotic effect that helps to reduce the viability of liver cancer cells.This study provides novel insights into the effects of As2O3 against liver cancer.