Long non-coding RNA opa-interacting protein 5 antisense transcript 1 (LncRNA OIP5-AS1) promoted cisplatin resistance in nasopharyngeal carcinoma via the miR-378a-3p/nicotinamide N-methyltransferase axis

被引:0
|
作者
Bai, Zhigang [1 ]
Zhang, Dongli [2 ]
Shi, Enhong [3 ]
机构
[1] Harbin Med Univ, Dept Otorhinolaryngol Head & Neck Surg, Affiliated Hosp 4, Harbin 150001, Heilongjiang, Peoples R China
[2] Heilongjiang Prov Hosp, Dept Emergency, Harbin 150036, Heilongjiang, Peoples R China
[3] Heilongjiang Prov Hosp, Dept Med Oncol, Harbin 150036, Heilongjiang, Peoples R China
关键词
Nasopharyngeal Carcinoma; Cisplatin Resistance; OIP5-AS1; miR-378a-3p; NNMT; SQUAMOUS-CELL CARCINOMA; CANCER; NANOPARTICLES; PROLIFERATION; DELIVERY;
D O I
10.1166/mex.2022.2219
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
LncRNAs involve in chemoresistance of human cancers. However, the role and molecular mechanisms of lncRNA OIP5-AS1 in the chemoresistance of NPC are still unexplored. In our study, upregulated OIP5AS1 was found in cisplatin (CDDP)-resistant NPC tumors and cell lines. Functional assays revealed OIP5AS1 knockdown suppressed malignant behaviors, but stimulated apoptosis of CDDP-resistant NPC cells. Furthermore, we demonstrated OIP5-AS1 positively regulated NNMT by directly targeting miR-378a-3p. In addition, its inhibition partially abolished the inhibitory effects of OIP5-AS1 silencing on malignancy of CDDPresistant NPC cells, whereas NNMT knockdown reverse these effects. In sum, our results indicated OIP5-AS1 contributed to the CDDP resistance of NPC by sponging miR-378a-3p to increase NNMT expression.
引用
收藏
页码:980 / 987
页数:8
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