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LncRNAs as novel indicators of patients' prognosis in stage i epithelial ovarian cancer: A retrospective and multicentric study

Authors :
Luca Beltrame
Enrico Sartori
Franco Odicino
Chiara Romualdi
Eliana Bignotti
Stefano Cagnin
Dionyssios Katsaros
Lorenzo Ceppi
Maurizia Mello-Grand
Giulia Caratti
Paolo Martini
Enrica Calura
Ilaria Craparotta
Antonella Ravaggi
Maurizio D'Incalci
Sergio Marchini
Laura Mannarino
Lara Paracchini
Patrizia Perego
Robert Fruscio
Costantino Mangioni
Giovanna Chiorino
C Ghimenti
Gabriele Sales
Martini, P
Paracchini, L
Caratti, G
Mello-Grand, M
Fruscio, R
Beltrame, L
Calura, E
Sales, G
Ravaggi, A
Bignotti, E
Odicino, F
Sartori, E
Perego, P
Katsaros, D
Craparotta, I
Chiorino, G
Cagnin, S
Mannarino, L
Ceppi, L
Mangioni, C
Ghimenti, C
D'Incalci, M
Marchini, S
Romualdi, C
Publication Year :
2017
Publisher :
American Association for Cancer Research Inc., 2017.

Abstract

Purpose: Stage I epithelial ovarian cancer (EOC) represents about 10% of all EOCs and is characterized by good prognosis with fewer than 20% of patients relapsing. As it occurs less frequently than advanced-stage EOC, its molecular features have not been thoroughly investigated. We have demonstrated that in stage I EOC miR-200c-3p can predict patients' outcome. In the present study, we analyzed the expression of long non-coding RNAs (lncRNA) to enable potential definition of a non-coding transcriptional signature with prognostic relevance for stage I EOC. Experimental Design: 202 snap-frozen stage I EOC tumor biopsies, 47 of which relapsed, were gathered together from three independent tumor tissue collections and subdivided into a training set (n = 73) and a validation set (n = 129). Median follow up was 9 years. LncRNAs' expression profiles were correlated in univariate and multivariate analysis with overall survival (OS) and progression-free survival (PFS). Results: The expression of lnc-SERTAD2-3, lnc-SOX4-1, lnc-HRCT1-1, and PVT1 was associated in univariate and multivariate analyses with relapse and poor outcome in both training and validation sets (P < 0.001). Using the expression profiles of PVT1, lnc-SERTAD2-3, and miR-200c-3p simultaneously, it was possible to stratify patients into high and low risk. The OS for high- and low-risk individuals are 36 and 123 months, respectively (OR, 15.55; 95% confidence interval, 3.81–63.36). Conclusions: We have identified a non-coding transcriptional signature predictor of survival and biomarker of relapse for stage I EOC. Clin Cancer Res; 23(9); 2356–66. ©2016 AACR.

Details

Language :
English
Database :
OpenAIRE
Accession number :
edsair.doi.dedup.....bc979bcd52043f84735f096c03177297