Expression of oncogenic long noncoding RNA PSMG3-antisense 1 in lung squamous cell carcinoma

被引:4
|
作者
Jin, E. [1 ]
Huang, Chao [1 ]
Zhang, Lei [1 ]
Chen, Shiyi [1 ]
Zhao, Xiaochen [1 ]
Ren, Zheng [1 ]
Fu, Hong [2 ]
机构
[1] Fourth Peoples Hosp Shenyang, Dept Med Oncol, Shenyang 110031, Liaoning, Peoples R China
[2] Fourth Peoples Hosp Shenyang, Dept Intervent Oncol, 20 Huanghe St, Shenyang 110031, Liaoning, Peoples R China
关键词
invasion; long noncoding RNA PSMG3 antisense 1; lung squamous cell carcinoma; migration; microRNA-143-3p; prognosis; proliferation; CANCER; PHASE-3;
D O I
10.3892/ol.2021.13012
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Lung squamous cell carcinoma (LUSC) is one of the most common subtypes of lung cancer that accounts for similar to 50% of all lung cancer cases. Long noncoding RNA (lncRNA) PSMG3-antisense (AS) 1 has been suggested to play an important role in various types of cancer. Therefore, the aim of the present study was to investigate the role of PSMG3-AS1 using clinical specimens and data from 130 patients with LUSC. The expression levels of PSMG3-AS1 and miR-143-3p were detected in LUSC specimens, and the correlation between lncRNA PSMG3-AS1 expression and patient clinical characteristics was analyzed. Cell Counting Kit-8, Transwell migration and invasion assays were used to investigate the functional role of PSMG3-AS1 in LUSC. The mechanism of PSMG3-AS1 on LUSC cells was also investigated using a luciferase activity assay with wild-type or mutated PSMG3-AS1. PSMG3-AS1 was found to be upregulated in LUSC, and high expression was associated with positive lymph node metastasis and a higher TNM stage. The results of multivariate Cox regression analysis revealed that PSMG3-AS1 may serve as an independent prognostic indicator in LUSC. Furthermore, inhibiting PSMG3-AS1 expression reduced tumor cell proliferative, migratory and invasive abilities. Moreover, PSMG3-AS1 was found to be closely associated with miR-143-3p in LUSC, and thus may become a potential prognostic marker and therapeutic target for the treatment of LUSC in the future.
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页数:7
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