实用医学杂志 ›› 2020, Vol. 36 ›› Issue (20): 2780-2785.doi: 10.3969/j.issn.1006⁃5725.2020.20.007

• 基础研究 • 上一篇    下一篇

依沙佐米通过mTOR/p70S6K信号通路诱导食管鳞癌细胞凋亡

杨亮,石科,李敏霞,郭丹   

  1. 河南医学高等专科学校微生物与免疫学教研室(郑州451191)
  • 出版日期:2020-10-20 发布日期:2020-10-25
  • 通讯作者: 郭丹E⁃mail:2658jiaxi@163.com
  • 基金资助:

    河南省高等学校重点科研项目(编号:18A310015);河南省高等职业学校青年骨干教师项目(编号:2019GZGG086);河南省医学科技攻关计划联合共建项目(编号:2018020529,LH⁃GJ20190716);河南省科技攻关计划项目(编号:192102310110)

Ixazomib induces apoptosis of esophageal squamous carcinoma cells through mTOR/p70S6K signaling pathway

YANG Liang,SHI Ke,LI Minxia,GUO Dan   

  1. Department of Microbiology and Immunology,Henan Medical College,Zhengzhou 451191,China
  • Online:2020-10-20 Published:2020-10-25
  • Contact: GUO Dan E⁃mail:2658jiaxi@163.com

摘要:

目的 探讨依沙佐米通过mTOR/p70S6K 信号通路诱导食管鳞癌细胞凋亡的机制。方法 用依沙佐米处理食管鳞癌细胞KYSE⁃140和KYSE⁃150,分别用CCK⁃8法和Edu法检测细胞增殖,流式细胞仪检测依沙佐米处理后KYSE⁃140和KYSE⁃150的细胞凋亡,以及caspase⁃3等凋亡因子的表达,RT⁃qPCR和Western blot检测依沙佐米处理后mTOR、p70S6K和4E⁃BP1的mRNA和蛋白表达水平,以及p⁃p70S6KThr421/Ser424 和p⁃4E⁃BP1Thr36 蛋白的表达。结果 依沙佐米可以抑制食管鳞癌细胞KYSE⁃140 和KYSE⁃150 的增殖,且存在剂量依赖性。流式细胞仪检测结果显示依沙佐米处理后,KYSE⁃140和KYSE⁃150细胞的凋亡率显著增加(P < 0.05),caspase⁃3活性显著增高(P < 0.05),处理组出现PARP的裂解产物cleaved PARP,而未处理组未见PARP的裂解,并且细胞凋亡激活物p⁃p38的表达升高(P < 0.05)。与对照组相比,依沙佐米处理组mTOR 的mRNA 和蛋白表达水平均显著下降(P < 0.05),p70S6K 和4E⁃BP1 的mRNA 表达水平显著下降(P < 0.05),且p⁃p70S6KThr421/Ser424和p⁃4E⁃BP1Thr36的表达显著下降(P < 0.05)。结论 依沙佐米可通过抑制mTOR/p70S6K信号通路诱导食管鳞癌细胞的凋亡。

关键词: 依沙佐米, 食管鳞癌细胞, mTOR/p70S6K信号通路, 细胞凋亡

Abstract:

Objective To investigate whether Ixazomib induces apoptosis of esophageal squamous carcino⁃ma cells through mTOR/p70S6K signaling pathway. Methods Esophageal squamous cell carcinoma cells KYSE⁃140 and KYSE⁃150 were treated by Ixazomib,followed by CCK⁃8 and Edu assays to examine the cell proliferation.Flow cytometry was used to detect apoptosis of KYSE⁃140 and KYSE⁃150 cells,and expressions of caspase⁃3 andother apoptotic factors. The mRNA and protein expression levels of mTOR,p70S6K and 4E⁃BP1 were examined byRT⁃qPCR and western blot. Expressions of p⁃p70S6KThr421/Ser424 and p⁃4E⁃BP1Thr36 were detected by westernblot. Results Proliferations of KYSE⁃140 and KYSE⁃150 cells were inhibited by Ixazomib treatment in a dose⁃dependent manner. After Ixazomib treatment ,apoptosis of KYSE⁃140 and KYSE⁃150 cells were significantlyinduced(P < 0.05)and the activity of caspase⁃3 was significantly increased(P < 0.05). The PARP was cleaved inIxazomib treatment group,whereas there was no PARP cleavage in control group. Also,the expression of apoptosisactivator p⁃p38 was significantly increased in Ixazomib treatment group(P < 0.05). Compared with the controlgroup,Ixazomib treatment caused inhibition of the mRNA and protein expression of mTOR(P < 0.05),decreasedexpression of p70S6K and 4E⁃BP1 mRNA expression(P < 0.05). Western blot results showed that expressions ofp⁃p70S6KThr421/Ser424 and p⁃4E⁃BP1Thr36 were significantly decreased(P < 0.05). Conclusion Ixazomibmay induce apoptosis of esophageal squamous carcinoma cells by inhibiting mTOR / p70S6K signaling pathway.

Key words: Ixazomib, esophageal squamous cell carcinoma, mTOR/p70S6K signaling pathway,
apoptosis