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作 者:李慧霞 尤伟波[1] 陈丽[1] 王建平[1] 邵初晓[1] LI Huixia;YOU Weibo;CHEN Li;WANG Jianping;SHAO Chuxiao(Department of Anorectal Surgery,The Fifth Affiliated Hospital of Wenzhou Medical University,Lishui 323000,China)
机构地区:[1]温州医科大学附属第五医院肛肠外科,浙江丽水323000
出 处:《中国现代应用药学》2021年第21期2659-2664,共6页Chinese Journal of Modern Applied Pharmacy
基 金:浙江省医药卫生科技计划项目(2020KY1087)。
摘 要:目的探讨AMPK在华蟾素(cinobufagin,CBG)诱导结直肠癌HCT116细胞发生免疫原性死亡的作用。方法体外培养结直肠癌HCT116细胞,并将细胞分为对照组、CBG组、CBG+AMPK抑制剂组(抑制剂组)和CBG+AMPK siRNA干扰组(干扰组);用MTT法检测细胞增殖,LIVE/DEAD^(TM) Viability/Cytotoxicity Kit试剂盒观察细胞死亡情况,流式细胞仪技术检测细胞凋亡比例、钙网蛋白(calreticulin,CRT)含量,ELISA法检测培养基中HMGB1含量,Western blotting方法检测AMPK、磷酸化的AMPK(p-AMPK)的表达水平。结果2.5,5,10,25,50,100,250,500 nmol·L^(-1)的CBG处理48 h后,细胞增殖抑制率显著增加,IC_(50)为(53.03±5.36)nmol·L^(-1)。25,50 nmol·L^(-1)的CBG显著增加p-AMPK表达。与对照组比较,CBG组细胞凋亡比例、cleaved-caspase 3表达、CRT和HMGB1含量增加,Bcl-2表达下降;与CBG组相比,抑制剂组和干扰组细胞凋亡比例、cleaved-caspase 3表达、CRT和HMGB1含量明显下降,Bcl-2表达增加。结论CBG通过激活AMPK诱发免疫原性死亡,抑制结直肠癌细胞的增殖。OBJECTIVE To investigate the role of AMPK in cinobufagin(CBG)induced immunogenic death of colorectal cancer HCT116 cells.METHODS The colorectal cancer HCT116 cells were cultured in vitro and divided into four group including control group,CBG group,CBG+AMPK inhibitor group(named inhibitor group)and CBG+AMPK siRNA group(named interference group).Cell survival was detected by MTT.The dying cells were detected by LIVE/DEAD^(TM) Viability/Cytotoxicity Kit.The apoptosis and calreticulin(CRT)content were detected by flow cytometry.The expression of AMPK,phosphorylated AMPK(p-AMPK)were detected by Western blotting.RESULTS After treatment with 2.5,5,10,25,50,100,250,500 nmol·L^(-1) CBG for 48 h,the inhibition rate of HCT116 increased significantly and the half-inhibitory concentration(IC_(50))was(53.03±5.36)nmol·L^(-1).Dosage of 25,50 nmol·L^(-1) CBG treatment significantly increased the expression of p-AMPK.Compared with control group,the apoptotic cells,the expression of cleaved-capapse3,the content of CRT and HMGB1increased,while the expression of Bcl-2 decreased in CBG group.Compared with CBG group,the apoptotic cells,the expression of cleaved-capapse3,the content of CRT and HMGB1 decreased,wherea the expression of Bcl-2 increased in inhibitor group and interference group.CONCLUSION CBG induces immunogenic death by activating AMPK and inhibits the proliferation of colorectal cancer cells.
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