检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:丁忠阳[1] 王柯[2] 梅丹[1] 吴昊天[1] 蒋盘强[1] 张朦晓 朱雪[2] 汪舒伟 DING Zhong-yang;WANG Ke;MEI Dan;WU Hao-tian;JIANG Pan-qiang;ZHANG Meng-xiao;ZHU Xue;WANG Shu-wei(Department of General Surgery,Wuxi TCM Hospital Affiliated to Nanjing University of Chinese Medicine,Wuxi 214071,Jiangsu ,China;Jiangsu Key Laboratory of Molecular Nuclear Medicine,Jiangsu Institute of Nuclear Medicine,Key Laboratory of Nuclear Medicine,National Health Commission of the People's Republic of China,Wuxi 214063,Jiangsu,China)
机构地区:[1]南京中医药大学附属无锡市中医医院普通外科,无锡214071 [2]江苏省原子医学研究所,国家卫生健康委核医学重点实验室,无锡214063
出 处:《中国现代手术学杂志》2019年第3期161-165,共5页Chinese Journal of Modern Operative Surgery
基 金:无锡市科学技术发展项目(CSE31N1513)
摘 要:目的 探讨IL-6介导的HIF-1α激活对人胃癌MKN45细胞裸鼠移植瘤顺铂耐药的影响。方法 通过接种人胃癌MKN45细胞建立人胃癌裸鼠移植瘤模型。将胃癌移植瘤裸鼠分为三组:对照组,顺铂组和顺铂+IL-6组,每组10只。给药4周后,取出瘤体测量瘤重及抑瘤率,并用Western-blot法检测肿瘤组织中相关蛋白的表达。结果 在瘤重方面,对照组>顺铂+IL-6组>顺铂组;在抑瘤率方面,顺铂组>顺铂+IL-6组,差异有统计学意义(P<0.05)。进一步研究发现IL-6诱导裸鼠移植瘤耐药主要通过激活HIF-1α,抑制下游凋亡通路(Bax,Bcl-2, Cleaved Caspase-9及Cleaved Caspase-3)的激活及诱导下游药物外排通路(P-gp和MRP1)的表达(P<0.05)。结论 IL-6干预可促进人胃癌MKN45细胞裸鼠移植瘤顺铂耐药,其机制主要通过激活HIF-1α及下游信号通路。Objective To investigate the effect of IL-6/HIF-1α activation on resistance to cisplatin in nude mice with subcutaneous xenograft of human gastric cancer MKN45 cells.Methods Human gastric cancer transplanted tumor models were established by injection of MKN45 cells on BALB /c nude mice.Transplanted tumor models were divided into three groups,the control group,cisplatin-treated group,and cisplatin/IL-6-treated group,with 10 mice for each.After 4-week treatment,the transplanted tumor weight was measured and tumor-inhibition rate were calculated.The expressions of related proteins were examined by western blot analysis.Results It was revealed that the weight of tumors was control group>cisplatin/IL-6-treated group>cisplatin-treated group (P<0.05).The tumor-inhibition rate of cisplatin/IL-6-treated group was significantly lower than that of cisplatin-treated group (P<0.05).Moreover,IL-6 mediated resistance of human gastric cancer transplanted tumors to cisplatin was induced by activating HIF-1α,inhibiting cell apoptotic pathway (Bax,Bcl-2,Cleaved Caspase-3 and Cleaved Caspase-9),and inducing drug efflux pathway (P-gp and MRP1).Conclusion IL-6 treatment promoted resistance of human gastric cancer transplanted tumors to cisplatin by inducing HIF-1α activation and affecting downstream signaling pathways.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.81