RETRACTED: MicroRNA-101 induces apoptosis in cisplatin-resistant gastric cancer cells by targeting VEGF-C (Retracted article. See vol. 24, pg. 694, 2021)

被引:23
|
作者
Li, Guangyan [1 ]
Yang, Fang [1 ]
Gu, Shiyu [2 ]
Li, Zhenjuan [1 ]
Xue, Minghui [3 ]
机构
[1] Xinxiang Med Univ, Affiliated Hosp 1, Dept Gastroenterol, Weihui 453100, Henan, Peoples R China
[2] Xinxiang Med Univ, Affiliated Hosp 3, Dept Gastroenterol, Xinxiang 453000, Henan, Peoples R China
[3] Xinxiang Med Univ, Affiliated Hosp 1, Dept Gen Surg, Weihui 453100, Henan, Peoples R China
关键词
gastric cancer; microRNA-101; cisplatin; drug resistance; vascular endothelial growth factor; MIR-101; EXPRESSION; PROLIFERATION; CHEMORESISTANCE; TRANSITION; EZH2;
D O I
10.3892/mmr.2015.4560
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Deregulation of microRNAs (miRNAs) is known to be associated with drug resistance in human cancers. However, the precise role of miR-101 in the cisplatin (DPP) resistance of human gastric cancer cells has not been elucidated, yet. The present study revealed that miR-101 was markedly down-regulated in gastric cancer cell lines compared to that in the normal gastric mucosa epithelial cell line GES1. Furthermore, a significant decrease in miR-101 levels, accompanied with an increased expression of vascular endothelial growth factor (VEGF)-C in DDP-resistant SGC7901 gastric cancer cells (SGC7901/DDP) compared with those in native SGC7901 cells was observed. In addition, forced overexpression of miR-101 significantly inhibited cell proliferation, while enhancing cisplatin-induced apoptosis of SGC7901/DDP cells. A luciferase reporter assay confirmed that VEGF-C was a direct target of miR-101 in SGC7901/DDP cells. Forced overexpression of miR-101 in SGC7901/DDP cells reduced the expression of VEGF-C, while knockdown of miR-101 expression significantly enhanced VEGF-C expression in SGC7901/DDP cells. Finally, overexpression of VEGF-C inhibited DDP-induced apoptosis in SGC7901 cells. In conclusion, the results of the present study suggested that miR-101 inhibited the proliferation and promoted DDP-induced apoptosis of DDP-resistant gastric cancer cells, at least in part via targeting VEGF-C.
引用
收藏
页码:572 / 578
页数:7
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