4.5 Article

Long non-coding RNA LINC00336 as an independent prognostic indicator and an oncogenic lncRNA in bladder cancer

Journal

ARCHIVES OF MEDICAL SCIENCE
Volume 19, Issue 2, Pages 478-487

Publisher

TERMEDIA PUBLISHING HOUSE LTD
DOI: 10.5114/aoms.2019.89661

Keywords

bladder cancer; LINC00336; long non-coding RNA; prognosis; apoptosis

Ask authors/readers for more resources

This study aimed to investigate the role of LINC00336 in the tumorigenesis of bladder cancer (BCa). LINC00336 was found to be significantly up-regulated in BCa tissues and cell lines. Knockdown of LINC00336 blocked cell proliferation and invasion, and induced cell cycle arrest and apoptosis. These findings suggested that LINC00336 may serve as an oncogene in the initiation and progression of BCa and could be a potential therapeutic target.
Introduction: Long non-coding RNAs (lncRNAs) have been implicated in the initiation and progression of malignant tumor. The aim of the present study was to investigate whether LINC00336 contributes to the tumorigenesis of bladder cancer (BCa). Material and methods: LncRNA expression profiling in BCa tissues was an-alyzed using lncRNA microarray. Cell viability, invasion and apoptosis were detected using CCK8, Transwell and Annexin V-fluorescein isothiocyanate/ propidium iodide (Annexin V-FITC) double staining, respectively. Results: LncRNA microarray and RT-qPCR revealed that LINC00336 was sig-nificantly up-regulated in BCa tissues and cell lines compared with the cor-responding control group. Kaplan-Meier and multivariate regression analysis demonstrated that LINC00336 could serve as an independent risk factor for predicting the prognosis of BCa patients. In vitro experimental measure-ments showed that knockdown of LINC00336 had the ability to block cell proliferation and invasion, as well as to induce cell cycle arrest and apoptosis. Conclusions: These findings indicated that LINC00336 might serve as an oncogene in the initiation and progression of BCa, and LINC00336 may be a valuable and promising therapeutic target for the treatment of BCa.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available