Long noncoding RNA PXN-AS1-L promotes non-small cell lung cancer progression via regulating PXN

被引:32
作者
Zhang, Zhifa [1 ]
Peng, Zhaohui [2 ,3 ]
Cao, Junying [4 ]
Wang, Jiaqi [5 ]
Hao, Yongyu [1 ]
Song, Kai [1 ]
Wang, Yan [1 ]
Hu, Wei [6 ]
Zhang, Xuesong [1 ]
机构
[1] Peoples Liberat Army Gen Hosp, Dept Orthopaed Surg, Beijing 100000, Peoples R China
[2] Second Mil Med Univ, Changzheng Hosp, Dept Radiol, Shanghai 200003, Peoples R China
[3] Jinan Mil Gen Hosp, Dept Radiol, Jinan 250031, Shandong, Peoples R China
[4] Gen Hosp Shenyang Mil Reg, Dept Ultrasonog, Shenyang 110016, Liaoning, Peoples R China
[5] China Med Univ, Dept Orthopaed Surg, Shenyang 110001, Liaoning, Peoples R China
[6] Second Mil Med Univ, Changhai Hosp, Dept Gen Surg, Shanghai 200433, Peoples R China
基金
中国国家自然科学基金;
关键词
Long noncoding RNA; Non-small-cell lung cancer; Proliferation; Migration; PXN; HEPATOCELLULAR-CARCINOMA; EXPRESSION; MANAGEMENT; EVOLUTION; APOPTOSIS; PAXILLIN; INVASION;
D O I
10.1186/s12935-019-0734-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundIncreasingly evidences suggest that long noncoding RNAs (lncRNAs) play important roles in various cancers. LncRNA PXN-AS1-L is recently revealed to act as on oncogene in liver cancer. However, the expression, functions, and mechanisms of action of PXN-AS-L in non-small cell lung cancer (NSCLC) remain unclear.MethodsThe expression of PXN-AS1-L in primary NSCLC tissues, NSCLC bone metastasis tissues, and cell lines was measured by quantitative real-time PCR. The correlations between PXN-AS1-L expression and clinicopathological characteristics of NSCLC patients were analyzed by Pearson Chi square test and log-rank test. The roles of PXN-AS1-L in cell viability, proliferation, apoptosis, and migration of NSCLC cells, and in vivo NSCLC tumor growth were investigated by a series of gain-of-function and loss-of-function assays. The regulatory roles of PXN-AS1-L on PXN were determined by quantitative real-time PCR and western blot.ResultsPXN-AS1-L was up-regulated in NSCLC tissues compared with noncancerous lung tissues, and PXN-AS1-L was further up-regulated in NSCLC bone metastasis tissues. Increased expression of PXN-AS1-L was positively associated with advanced TNM stages and poor prognosis. Gain-of-function and loss-of-function assays showed that PXN-AS1-L increased cell viability, promoted cell proliferation, inhibited cell apoptosis, and promoted cell migration of NSCLC cells. Xenograft assays showed that PXN-AS1-L also promoted NSCLC tumor growth in vivo. Mechanistically, we found that PXN-AS1-L, as an antisense transcript of PXN, up-regulated the expression of PXN. PXN was also up-regulated in NSCLC tissues. The expression of PXN and PXN-AS1-L was positively correlated in NSCLC tissues. Furthermore, PXN knockdown attenuated the roles of PXN-AS1-L in increasing cell viability, promoting cell proliferation, inhibiting cell apoptosis, and promoting cell migration of NSCLC cells.ConclusionsOur data revealed that PXN-AS1-L is up-regulated and acts as an oncogene in NSCLC via up-regulating PXN. Our data suggested that PXN-AS1-L might serve as a potential prognostic biomarker and therapeutic target for NSCLC.
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页数:13
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