首页> 外文期刊>Biochemistry and Cell Biology >Synergistic effects of autophagy inhibitors combined with cisplatin against cisplatin-resistant nasopharyngeal cancer cells
【24h】

Synergistic effects of autophagy inhibitors combined with cisplatin against cisplatin-resistant nasopharyngeal cancer cells

机译:自噬抑制剂联合顺铂对顺铂抗性鼻咽癌细胞的协同作用

获取原文
获取原文并翻译 | 示例
           

摘要

This study explored the synergistic effects of autophagy inhibitors combined with cisplatin against cisplatin-resistant nasopharyngeal cancer cells by treating HNE-1 and cisplatin (diamminedichloroplatinum; DDP)-resistant HNE1/DDP nasopharyngeal cancer cell lines with DDP, autophagy inhibitors, or a combination of autophagy inhibitors and DDP. Cell viability was determined via MTT (colorimetric) and colony-forming assays, and the rate of apoptosis was determined using propidium iodide (PI) and annexin V double-staining. The expressions of proteins were determined by Western blotting. For our in-vivo studies, a murine xenograft model was established to evaluate the anti-tumor effects of the combination of autophagy inhibitor and DDP. The results showed that treatment with DDP increased the expressions of ATP-binding cassette sub-family B member 1 (ABCB1), ATP Binding Cassette Subfamily C Member 1 (ABCC1), and P-glycoprotein 1 (P-gp) in the HNE1/DDP cell lines. Treatment with chloroquine decreased the expression levels of ABCB1, ABCC1, and P-gp, and increased the formation of LC3-II and the expression levels of p62 in the HNE1/DDP cells. Additionally, the combination of autophagy inhibitors and DDP produced a synergistic effect on DDP-induced cell death and apoptosis. Furthermore, the combination of the autophagy inhibitor and DDP showed significant anti-tumor effects in the xenograft mouse model. In summary, autophagy inhibitors show synergistic anti-tumor effects with DDP in vitro against DDP-resistant nasopharyngeal cancer cells and in vivo in our xenograft murine model.
机译:本研究探讨了通过治疗HNE-1和顺铂(Diammoledicholloplatinum; DDP)-Resistant HNE1 / DDP Noophary癌细胞系与DDP,自噬抑制剂或组合来探讨了自噬抑制剂与顺铂抗性鼻咽癌细胞联合对顺铂抗性鼻咽癌细胞的协同效应。自噬抑制剂和DDP。通过MTT(比色)和菌落形成测定法测定细胞活力,使用碘化丙啶(PI)和膜蛋白V双染色测定细胞凋亡率。通过蛋白质印迹测定蛋白质的表达。对于我们的体内研究,建立了鼠异种移植模型,以评估自噬抑制剂和DDP组合的抗肿瘤作用。结果表明,DDP处理增加了HNE1 /中的ATP结合盒子族B成员1(ABCB1),ATP结合盒,ATP结合饼干亚家族C构件1(ABCC1)和P-Glo​​totine1(P-GP)的表达式。 DDP细胞系。用氯喹处理降低了ABCB1,ABCC1和P-GP的表达水平,并增加了HNE1 / DDP细胞中LC3-II的形成和P62的表达水平。另外,自噬抑制剂和DDP的组合对DDP诱导的细胞死亡和细胞凋亡产生了协同作用。此外,自噬抑制剂和DDP的组合在异种移植小鼠模型中显示出显着的抗肿瘤作用。总之,自噬抑制剂对DDP抗性鼻咽癌细胞的DDP和体内患有协同抗肿瘤作用和在我们的异种移植小鼠模型中。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号