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Research Paper|Volume 11, Issue 17|pp 6930—6940

An eight-long non-coding RNA signature as a candidate prognostic biomarker for bladder cancer

Penghu Lian1, Qian Wang2, Ya Zhao3, Cheng Chen4, Xiacheng Sun4, Hanzhong Li1, Jianhua Deng1, Hongmei Zhang5, Zhigang Ji1, Xuebin Zhang1, Qichao Huang4
  • 1Department of Urology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College (CAMS & PUMC), Beijing 100730, China
  • 2Department of General Surgery, Tangdu Hospital, Fourth Military Medical University, Xi’an 710032, China
  • 3Biomedicine Application Laboratory, School of Life Science and Technology, Xidian University, Xi’an 710038, China
  • 4State Key Laboratory of Cancer Biology and Experimental Teaching Center of Basic Medicine, Fourth Military Medical University, Xi’an 710032, China
  • 5Department of Clinical Oncology, Xijing Hospital, Fourth Military Medical University, Xi’an 710032, China
* Equal contribution
Received: January 7, 2019Accepted: August 16, 2019Published: September 3, 2019

Copyright © 2019 Lian et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

Backgroud: Bladder cancer (BLCA) is one of the most fatal types of cancer worldwide. However, there are limited methods for us to provide a prognostic prediction of BLCA patients. Therefore, we aimed at developing a lncRNA signature to improve the prognosis prediction of BLCA.

Results: An eight-lncRNA signature was significantly associated with recurrence free survival in BLCA patients from both discovery and validation groups. Furthermore, genes involved in the signature were enriched in extracellular matrix organization pathway. Finally, functional experiments demonstrated that six out of the eight lncRNAs significantly regulated the invasion of BLCA cells.

Method: A total of 343 BLCA patients from The Cancer Genome Atlas (TCGA) were employed and randomly divided into training (n=172) and validating (n=171) groups. The lncRNA expression profiles of BLCA patients were screened and a risk-score formula were created and validated according to the Cox regression analysis. Next, WGCNA method was employed to cluster genes that highly correlated with the risk scores based on the profiling data of TCGA dataset and transwell assay was also performed to further investigate the role of these lncRNAs.

Conclusions: Our results suggested that the eight-lncRNA signature was a candidate prognostic biomarker for predicting tumor recurrence of patients with BLCA.