miR-149 contributes to resistance of 5-FU in gastric cancer via targeting TREM2 and regulating β-catenin pathway

被引:14
|
作者
Wang, Xiao-yan [1 ]
Zhou, Yi-chan [3 ]
Wang, Yan [1 ]
Liu, Yun-yun [1 ]
Wang, Yu-xin [1 ]
Chen, Dan-dan [1 ]
Fan, Yu [2 ]
机构
[1] First Peoples Hosp Suqian, Dept Gastroenterol, Suqian 223800, Jiangsu, Peoples R China
[2] Jiangsu Univ, Canc Inst, Affiliated Peoples Hosp, Zhenjiang 212002, Jiangsu, Peoples R China
[3] Nanjing Med Univ, Dept Geriatr, Jiangsu Prov Key Lab Geriatr, Affiliated Hosp 1, Nanjing 210006, Jiangsu, Peoples R China
关键词
Drug resistance; Gastric cancer; miR-149; 5-FU; CISPLATIN RESISTANCE; MULTIDRUG-RESISTANCE; CELLS; PROLIFERATION; APOPTOSIS; MICRORNAS; REVERSES; BCL2;
D O I
10.1016/j.bbrc.2020.05.135
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Drug resistance remains the unresolved obstacle for gastric cancer (GC) treatment. Recently more and more studies have shown that microRNAs are involved in cancer resistance and could apply to drug resistance therapy in tumors. The relationship between miR-149 and 5-fluorouracil (5-FU) resistance in GC remains unclear. Here we detected miR-149 expression in 5-FU resistance tumor tissues and cell lines, and found that miR-149 expression is upregulated in AGS/5-FU cells compared with AGS cells. Further experiments indicated that overexpression of miR-149 can alleviate 5-FU-induced apoptosis and proliferation inhibition by targeting TREM2. It was also confirmed that TREM2 regulated 5-FU resistance through beta-catenin pathway. Generally speaking, our results indicated that miR-149 contributes to resistance of 5-FU in gastric cancer via targeting TREM2 and regulating beta-catenin pathway. (C) 2020 Published by Elsevier Inc.
引用
收藏
页码:329 / 335
页数:7
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