Double-negative feedback loop between long non-coding RNA TUG1 and miR-145 promotes epithelial to mesenchymal transition and radioresistance in human bladder cancer cells.

Abstract:

:LncRNAs have a critical role in the regulation of cellular processes such as cancer progression and metastasis. In the present study, we confirmed that TUG1 was overexpressed in bladder cancer tissues and established cell lines. Knockdown of TUG1 inhibited bladder cancer cell metastasis both in vitro and in vivo. Furthermore, we found that TUG1 promoted cancer cell invasion and radioresistance through inducing epithelial-to-mesenchymal transition (EMT). Interestingly, TUG1 decreased the expression of miR-145 and there was a reciprocal repression between TUG1 and miR-145 in an Argonaute2-dependent manner. ZEB2 was identified as a down-stream target of miR-145 and TUG1 exerted its function through the miR-145/ZEB2 axis. In summary, our data indicated that blocking TUG1 function may be an effective anti-cancer therapy.

journal_name

FEBS Lett

journal_title

FEBS letters

authors

Tan J,Qiu K,Li M,Liang Y

doi

10.1016/j.febslet.2015.08.020

subject

Has Abstract

pub_date

2015-10-07 00:00:00

pages

3175-81

issue

20 Pt B

eissn

0014-5793

issn

1873-3468

pii

S0014-5793(15)00720-6

journal_volume

589

pub_type

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