三氧化二砷
碘化丙啶
细胞凋亡
化学
活力测定
癌症研究
MTT法
药理学
细胞毒性T细胞
自噬
程序性细胞死亡
癌细胞
细胞毒性
癌症
医学
生物化学
内科学
体外
作者
Pei‐Ju Wu,I‐Lun Hsin,Wei-Li Hung,Maw‐Sheng Lee,Po-Hui Wang,Jiunn‐Liang Ko
标识
DOI:10.1016/j.cbi.2022.110177
摘要
Cyclosporin A is an immunosuppressive drug with anti-cancer effect. Arsenic trioxide (As2O3), a well-known cancer-inhibiting drug, induced cytotoxicity via apoptosis and autophagy. The aim of this study is to evaluate the effect of combinational treatment with cyclosporin A and arsenic trioxide on cell viability inhibition in cervical cancer cells. Using MTT assay and combination index, combinational treatment with cyclosporin A and arsenic trioxide induced a synergistic cytotoxic effect in Caski and SiHa cells. Cyclosporin A and arsenic trioxide triggered cell death via non-apoptotic pathway by using annexin V/propidium iodide (PI) assay. Cyclosporin A and arsenic trioxide combined treatment decreased mitochondrial membrane potential and increase reactive oxygen species (ROS) generation. This co-treatment increased LC3B-II expression and autophagosome formation in cervical cancer cells. This study first demonstrated that combinational treatment with cyclosporin A and As2O3 trigger synergistic cytotoxic effect via autophagy in cervical cancer cells.
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