RETRACTED: Downregulation of ribophorin II suppresses tumor growth, migration, and invasion of nasopharyngeal carcinoma (Retracted article. See vol. 16, pg. 541, 2023)

被引:9
作者
Hong, Feilong [1 ]
Li, Yong [1 ]
Ni, Haifeng [1 ]
Li, Jing [1 ]
机构
[1] Hangzhou First Peoples Hosp, Dept Otolaryngol, 261 Huansha Rd, Hangzhou 310000, Zhejiang, Peoples R China
关键词
siRNA-RPN2; nasopharyngeal carcinoma; migration; invasion; MMP2; MMP9; SIGNALING PATHWAY; CELL INVASION; PROLIFERATION; ACTIVATION; KNOCKDOWN; APOPTOSIS; PROMOTES; MMP2;
D O I
10.2147/OTT.S158355
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: It has been reported that ribophorin II (RPN2) expression is increased in many cancers, but the role of RPN2 in nasopharyngeal carcinoma (NPC) remains unclear. Patients and methods: This study found that the expression of RPN2 is increased dramatically in NPC tissues of patients compared with that in the adjacent normal tissues. This study attempted at understanding the effect of siRNA-RPN2 treatment on the migration and invasion of NPC cell lines CNE2 and HNE1. Results: RT-PCR and Western blotting showed that RPN2 was highly expressed in CNE2 and HNE1 cells. siRNA-RPN2 treatment significantly inhibited cell viability at 24 and 48 h compared with the control group. Results of the transwell assay showed that, compared to the control groups, migration and invasion of the cells treated with siRNA-RPN2 decreased markedly. In addition, compared to the control groups, caspase-3, caspase-9, and E-cadherin expression levels increased and MMP 2 expression decreased significantly in the siRNA-RPN2-treated group. Phosphorylation of AKT and P13K was also inhibited after siRNA-RPN2 treatment. Conclusion: siRNA-RPN2 can effectively inhibit the invasion and migration of human NPC cells via AKT/PI3K signaling. This can serve as a novel strategy for NPC treatment.
引用
收藏
页码:3485 / 3494
页数:10
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