tRF-Leu-CAG promotes cell proliferation and cell cycle in non-small cell lung cancer

被引:180
|
作者
Shao, Yang [1 ,2 ,3 ]
Sun, Qiangling [4 ]
Liu, Xiaomin [1 ]
Wang, Ping [1 ]
Wu, Renqi [1 ,5 ]
Ma, Zhongliang [1 ]
机构
[1] Shanghai Univ, Lab Noncoding RNA & Canc, Sch Life Sci, Shanghai, Peoples R China
[2] Fudan Univ, Inst Canc, Shanghai Canc Ctr, Shanghai, Peoples R China
[3] Fudan Univ, Shanghai Med Coll, Dept Oncol, Shanghai, Peoples R China
[4] Shanghai Jiao Tong Univ, Shanghai Chest Hosp, Cent Lab, Shanghai, Peoples R China
[5] Shanghai Univ, Expt Ctr Life Sci, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
cell cycle; diagnostic biomarker; NSCLC; proliferation; tRF-Leu-CAG; INDUCED TRANSFER-RNA; FRAGMENTS; TETRAHYMENA; PROGRESSION; EXPRESSION; CARCINOMA; CLEAVAGE; STRESS;
D O I
10.1111/cbdd.12994
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
tRNA-derived RNA fragments (tRFs), non-coding single-stranded RNAs with 14-35 nt in length, were found to play important roles in gene regulation, even in carcinogenesis. In this study, we investigated the expression of tRF-Leu-CAG in human non-small cell lung cancer (NSCLC) and its function in the cell proliferation and cell cycle of NSCLC. The expression level of tRF-Leu-CAG was detected in NSCLC tissues, cell lines, and sera. tRF-Leu-CAG RNA levels were higher in NSCLC tumor tissues than in normal tissues, and also upregulated in NSCLC cell lines. A significant relationship was observed between stage progression and tRF-Leu-CAG in NSCLC sera. We found that in H1299 cells, inhibition of tRF-Leu-CAG suppressed cell proliferation and impeded cell cycle. AURKA was also repressed with the knockdown of tRF-Leu-CAG. Thus, our study revealed that tRF-Leu-CAG may be involved in regulating AURKA and could be a new diagnostic marker and potential therapeutic target in NSCLC.
引用
收藏
页码:730 / 738
页数:9
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