MicroRNA-126 increases chemosensitivity in drug-resistant gastric cancer cells by targeting EZH2

被引:52
|
作者
Wang, Ping [1 ]
Li, Ziqiu [2 ]
Liu, Haide [3 ]
Zhou, Dongmei [1 ]
Fu, Aiqin [1 ]
Zhang, Enning [1 ]
机构
[1] Yantaishan Hosp, Dept Oncol, 91 Jiefang Rd, Yantai 264000, Shandong, Peoples R China
[2] Peoples Hosp Rushan City, Dept Gen Surg, Rushan City 264500, Shandong, Peoples R China
[3] Yantaishan Hosp, Dept Radiat Oncol, Yantai 264000, Shandong, Peoples R China
关键词
miR-126; Chemosensitivity; EZH2; Gastric cancer; TUMOR-SUPPRESSOR; EXPRESSION; MIR-126; PROLIFERATION; SIGNATURES; MIGRATION; INVASION;
D O I
10.1016/j.bbrc.2016.09.040
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
Chemotherapeutic insensitivity is a significant barrier for effective treatment of gastric cancer (GC). Recently, emerging evidence has demonstrated that microRNAs (miRNAs) are critically involved in drug resistance. Here, by a large-scale screen, we noticed low expression of miR-126 in the drug-resistant GC cell lines SGC7901/VCR and SGC7901/ADR compared with their parental cell line SGC7901. Ectopic expression of miR-126 increased sensitivity of SGC7901/VCR and SGC7901/ADR cells to vincristine (VCR) and adriamycin (ADR). Mechanistically, Enhancer of Zeste Homolog 2 (EZH2) was identified as a direct target of miR-126. Genetic silencing of EZH2 mirrored the effects of miR-126 in drug resistance, and restoration of EZH2 blocked the inhibitory effect of miR-126 on GC. Taken together, our results suggest that miR-126 is a tumor suppressor by sensitizing GC cells to chemotherapy and provide a potential therapeutic approach in cancer treatment. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:91 / 96
页数:6
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