Inhibition of Mnk-eIF4E pathway sensitizes the efficacy to chemotherapy in anaplastic thyroid cancer

被引:13
|
作者
Hu, Kun [1 ]
Zhang, Juan [2 ]
Yu, Min [3 ]
Xiong, Chang'e [4 ]
机构
[1] Yangtze Univ, Jingzhou Cent Hosp, Thyroid Surg Dept, Clin Med Coll 2, Jingzhou, Peoples R China
[2] Yangtze Univ, Jingzhou Cent Hosp, Dept Endocrinol, Clin Med Coll 2, Jingzhou, Peoples R China
[3] Yangtze Univ, Jingzhou Cent Hosp, Galactophore Dept, Clin Med Coll 2, Jingzhou, Peoples R China
[4] Hubei Univ Sci & Technol, Sch Basic Med Sci, Xianning, Peoples R China
关键词
chemotherapy; eIF4E; Mnk; thyroid cancer; CELL-GROWTH; TRANSLATION; APOPTOSIS; PHOSPHORYLATION; PROGRESSION; CARCINOMA; THERAPY; EIF4E; LINES; MNKS;
D O I
10.2217/fon-2016-0320
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aim: We investigated whether MAPK-interacting kinase (Mnk) inhibition sensitizes anaplastic thyroid cancer (ATC) cellular response to chemotherapy. Materials & methods: In vitro and in vivo methods were used to examine the combinatory effects of cisplatin with Mnk inhibition and its underlying mechanism. Results: Mnk inhibition by pharmacological or genetic approaches inhibits proliferation and induces apoptosis of ATC cells and enhances the effects of cisplatin in in vitro and in vivo. Mechanistically, cisplatin increases eIF4E phosphorylation in a dose-and time-dependent manner in ATC cells. Mnk inhibitors sensitize the efficacy of cisplatin by inhibiting cisplatin-induced eIF4E phosphorylation. Conclusion: Targeting Mnk-eIF4E pathway provides a therapeutic strategy by sensitizing ATC response to chemotherapeutic drug.
引用
收藏
页码:489 / 498
页数:10
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