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SP1-induced lncRNA TINCR overexpression contributes to colorectal cancer progression by sponging miR-7-5p
Author(s) -
Shaojun Yu,
Da Wang,
Yingkuan Shao,
Teng Zhang,
Haiting Xie,
Xiaomeng Jiang,
Qun Deng,
Yurong Jiao,
Jinhua Yang,
Cai Cheng,
Lifeng Sun
Publication year - 2019
Publication title -
aging
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.473
H-Index - 90
ISSN - 1945-4589
DOI - 10.18632/aging.101839
Subject(s) - gene knockdown , colorectal cancer , downregulation and upregulation , biology , cancer research , biomarker , metastasis , pi3k/akt/mtor pathway , cancer , microrna , long non coding rna , signal transduction , cell culture , gene , genetics
Mounting evidences have indicated that long noncoding RNAs (lncRNAs) play pivotal roles in human diseases, especially in cancers. Recently, TINCR was proposed to be involved in tumor progression. However, its role in colorectal cancer (CRC) remains elusive. In our study, we found that SP1-induced TINCR was significantly upregulated in CRC tissues and cell lines. Moreover, cox multivariate survival analysis revealed that high TINCR was an independent predictor of poor overall survival (OS). Functionally, knockdown of TINCR obviously suppressed CRC cells proliferation, migration and invasion in vitro, and inhibited CRC cells growth and metastasis in vivo. Mechanistically, we identified TINCR could act as a miR-7-5p sponge using RNA pull down, luciferase reporter and RIP assays. Furthermore, we showed that TINCR might promote CRC progression via miR-7-5p-mediated PI3K/Akt/mTOR signaling pathway. Lastly, we revealed that plasma TINCR expression was upregulated in CRC when compared to healthy controls and could be a promising diagnostic biomarker for CRC. Based on above results, our data indicated that TINCR might serve as a potential diagnostic and prognostic biomarker for CRC.

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