scholarly journals Long Noncoding RNA MALAT1 Promotes Aggressive Renal Cell Carcinoma through Ezh2 and Interacts with miR-205

2015 ◽  
Vol 75 (7) ◽  
pp. 1322-1331 ◽  
Author(s):  
Hiroshi Hirata ◽  
Yuji Hinoda ◽  
Varahram Shahryari ◽  
Guoren Deng ◽  
Koichi Nakajima ◽  
...  
Author(s):  
Wang He ◽  
Guangzheng Zhong ◽  
Pei Wang ◽  
Chun Jiang ◽  
Ning Jiang ◽  
...  

2019 ◽  
Vol 10 (19) ◽  
pp. 4662-4670
Author(s):  
Fan Yang ◽  
Qingjian Wu ◽  
Le Zhang ◽  
Wei Xie ◽  
Xiaoli Sun ◽  
...  

2019 ◽  
Vol 8 (6) ◽  
pp. 2886-2896 ◽  
Author(s):  
Qianwei Xing ◽  
Ran Li ◽  
Aiming Xu ◽  
Zhiqiang Qin ◽  
Jinyuan Tang ◽  
...  

2020 ◽  
Vol 29 ◽  
pp. 096368972096441
Author(s):  
Xiaoqiang Zhai ◽  
Yan Wu ◽  
Zhenlong Wang ◽  
Dawei Zhao ◽  
Hecheng li ◽  
...  

Renal cell carcinoma (RCC) is the most common type of kidney cancer with rising incidence. Long noncoding RNA (lncRNA) LINC01133 is a novel lncRNA that is involved in the development of several types of cancers. However, the role of LINC01133 in RCC has not been reported. Thus, in this study, we investigated the functions of LINC01133 in RCC. The qualitative real-time polymerase chain reaction analysis was performed to examine the levels of LINC01133 in RCC tissues and adjacent tissues, as well as RCC cell lines. The results showed that LINC01133 was highly expressed in RCC tissue specimens and cell lines. Downregulation of LINC01133 significantly inhibited the proliferation, migration, and invasion of RCC cells. Further mechanistic investigations proved that LINC01133 directly interacted with microRNA (miR)-30b-5p and regulated the miR-30b-5p expression in RCC cell lines. Moreover, miR-30b-5p exhibited tumor-suppressive activity in RCC cell lines, which was mediated by targeting Ras-related protein Rab-3D (Rab3D). In vivo study showed that LINC01133 knockdown suppressed tumor growth in the nude mice. Taken together, these findings indicated that LINC01133 might be an oncogene in RCC through regulation of the miR-30b-5p/Rab3D axis. Thus, LINC01133 might serve as a potential therapeutic target for the treatment of RCC.


Cell Cycle ◽  
2017 ◽  
Vol 16 (22) ◽  
pp. 2212-2219 ◽  
Author(s):  
Xing Zeng ◽  
Zhiquan Hu ◽  
Xinwen Ke ◽  
Huake Tang ◽  
Bolin Wu ◽  
...  

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