LncRNA-UCA1 exerts oncogenic functions in non-small cell lung cancer by targeting miR-193a-3p

被引:396
作者
Nie, Wei [1 ]
Ge, Hui-juan [2 ]
Yang, Xiao-qun [2 ]
Sun, Xiangjie [2 ]
Huang, Hai [1 ]
Tao, Xia [3 ]
Chen, Wan-sheng [3 ]
Li, Bing [1 ]
机构
[1] Second Mil Med Univ, Shanghai Changzheng Hosp, Dept Resp Med, Shanghai 200003, Peoples R China
[2] Fudan Univ, Shanghai Canc Ctr, Dept Pathol, Shanghai 200032, Peoples R China
[3] Second Mil Med Univ, Shanghai Changzheng Hosp, Dept Pharm, Shanghai 200003, Peoples R China
关键词
lncRNA; UCA1; Non-small cell lung cancer; miR-193a-3p; ERBB4; LONG NONCODING RNA; CARCINOMA-ASSOCIATED; UCA1; CONTRIBUTES; MARKER;
D O I
10.1016/j.canlet.2015.11.024
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Recently, the long non-coding RNA (lncRNA) urothelial carcinoma-associated 1 (UCA1) has been identified as an oncogenic gene in multiple human tumor entitles, and dysregulation of UCA1 was tightly linked to carcinogenesis and cancer progression. However, whether the aberrant expression of UCA1 in non small cell lung cancer (NSCLC) is associated with malignancy, metastasis or prognosis has not been characterized. In this study, we found that UCA1 was upregulated in NSCLC tissues. Higher expression of UCA1 led to a significantly poorer survival time, and multivariate analysis revealed that UCA1 was an independent risk factor of prognosis. UCA1 overexpression enhanced, whereas UCA1 silencing impaired the proliferation and colony formation of NSCLC cells. Moreover, mechanistic investigations showed that UCA1 upregulated the expression of miR-193a-3p target gene ERBB4 through competitively 'spongeing' miR-193a-3p. Overall, we concluded that UCA1 functions as an oncogene in NSCLC, acting mechanistically by upregulating ERBB4 in part through 'spongeing' miR-193a-3p. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:99 / 106
页数:8
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