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High Expression of HULC Is Associated with Poor Prognosis in Osteosarcoma Patients.

Authors :
Vanessa Regina Maciel Uzan
André van Helvoort Lengert
Érica Boldrini
Valter Penna
Cristovam Scapulatempo-Neto
Carlos Alberto Scrideli
Alberto Paiva de Moraes Filho
Carlos Eduardo Bezerra Cavalcante
Cleyton Zanardo de Oliveira
Luiz Fernando Lopes
Daniel Onofre Vidal
Source :
PLoS ONE, Vol 11, Iss 6, p e0156774 (2016)
Publication Year :
2016
Publisher :
Public Library of Science (PLoS), 2016.

Abstract

Osteosarcoma (OS) is the most common primary bone cancer in childhood. OS is an aggressive disease, and metastatic patients evolve with very poor clinical outcomes. Genetically, OSs are extremely complex tumors, and the related metastatic process is not well understood in terms of the biology of the disease. In this context, long non-coding RNAs (lncRNAs) have emerged as an important class of gene expression regulators that play key roles in the invasion and metastasis of several human tumors. Here, we evaluated the expression of HULC, which is an lncRNA that is associated with the tumor metastatic process, and assessed its potential role as a prognostic marker in OS. HULC expression was evaluated in primary OS samples using real-time RT-PCR. HULC expression status was determined by receiver operating characteristic (ROC) analysis, and its association with survival was assessed using the Kaplan-Meier method. The HULC expression level was not significantly associated with the clinicopathological characteristics of the OS patients. However, our data demonstrated that higher levels of expression of HULC were associated with lower survival rates in OS patients, both in terms of overall and event-free survival. Elevated HULC expression was associated with poor clinical outcomes among the OS patients, which suggests that HULC could be a potential prognostic biomarker in OS.

Subjects

Subjects :
Medicine
Science

Details

Language :
English
ISSN :
19326203
Volume :
11
Issue :
6
Database :
Directory of Open Access Journals
Journal :
PLoS ONE
Publication Type :
Academic Journal
Accession number :
edsdoj.51ea25e1ffb5421bbca3f693f4cc1f2a
Document Type :
article
Full Text :
https://doi.org/10.1371/journal.pone.0156774