Cargando…

The lncRNAs RP1-261G23.7, RP11-69E11.4 and SATB2-AS1 are a novel clinical signature for predicting recurrent osteosarcoma

Background: Osteosarcoma is the most common primary bone malignancy in children and adolescents. In order to find factors related to its recurrence, and thus improve recovery prospects, a powerful clinical signature is needed. Long noncoding RNAs (lncRNAs) are essential in osteosarcoma processes and...

Descripción completa

Detalles Bibliográficos
Autores principales: Ying, Tang, Dong, Jin-ling, Yuan, Cen, Li, Peng, Guo, Qingshan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6944665/
https://www.ncbi.nlm.nih.gov/pubmed/31850493
http://dx.doi.org/10.1042/BSR20191251
_version_ 1783485053638017024
author Ying, Tang
Dong, Jin-ling
Yuan, Cen
Li, Peng
Guo, Qingshan
author_facet Ying, Tang
Dong, Jin-ling
Yuan, Cen
Li, Peng
Guo, Qingshan
author_sort Ying, Tang
collection PubMed
description Background: Osteosarcoma is the most common primary bone malignancy in children and adolescents. In order to find factors related to its recurrence, and thus improve recovery prospects, a powerful clinical signature is needed. Long noncoding RNAs (lncRNAs) are essential in osteosarcoma processes and development, and here we report significant lncRNAs to aid in earlier diagnosis of osteosarcoma. Methods: A univariate Cox proportional hazards regression analysis and a multivariate Cox regression analysis were used to analyze osteosarcoma patients’ lncRNA expression data from the Therapeutically Applicable Research To Generate Effective Treatments (TARGET), a public database. Results: A lncRNA signature consisting of three lncRNAs (RP1-261G23.7, RP11-69E11.4 and SATB2-AS1) was selected. The signature was used to sort patients into high-risk and low-risk groups with meaningful recurrence rates (median recurrence time 16.80 vs. >128.22 months, log-rank test, P<0.001) in the training group, and predictive ability was validated in a test dataset (median 16.32 vs. >143.80 months, log-rank test, P=0.006). A multivariate Cox regression analysis showed that the significant lncRNA was an independent prognostic factor for osteosarcoma patients. Functional analysis suggests that these lncRNAs were related to the PI3K-Akt signaling pathway, the Wnt signaling pathway, and the G-protein coupled receptor signaling pathway, all of which have various, important roles in osteosarcoma development. The significant 3-lncRNA set could be a novel prediction biomarker that could aid in treatment and also predict the likelihood of recurrence of osteosarcoma in patients.
format Online
Article
Text
id pubmed-6944665
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Portland Press Ltd.
record_format MEDLINE/PubMed
spelling pubmed-69446652020-01-09 The lncRNAs RP1-261G23.7, RP11-69E11.4 and SATB2-AS1 are a novel clinical signature for predicting recurrent osteosarcoma Ying, Tang Dong, Jin-ling Yuan, Cen Li, Peng Guo, Qingshan Biosci Rep Diagnostics & Biomarkers Background: Osteosarcoma is the most common primary bone malignancy in children and adolescents. In order to find factors related to its recurrence, and thus improve recovery prospects, a powerful clinical signature is needed. Long noncoding RNAs (lncRNAs) are essential in osteosarcoma processes and development, and here we report significant lncRNAs to aid in earlier diagnosis of osteosarcoma. Methods: A univariate Cox proportional hazards regression analysis and a multivariate Cox regression analysis were used to analyze osteosarcoma patients’ lncRNA expression data from the Therapeutically Applicable Research To Generate Effective Treatments (TARGET), a public database. Results: A lncRNA signature consisting of three lncRNAs (RP1-261G23.7, RP11-69E11.4 and SATB2-AS1) was selected. The signature was used to sort patients into high-risk and low-risk groups with meaningful recurrence rates (median recurrence time 16.80 vs. >128.22 months, log-rank test, P<0.001) in the training group, and predictive ability was validated in a test dataset (median 16.32 vs. >143.80 months, log-rank test, P=0.006). A multivariate Cox regression analysis showed that the significant lncRNA was an independent prognostic factor for osteosarcoma patients. Functional analysis suggests that these lncRNAs were related to the PI3K-Akt signaling pathway, the Wnt signaling pathway, and the G-protein coupled receptor signaling pathway, all of which have various, important roles in osteosarcoma development. The significant 3-lncRNA set could be a novel prediction biomarker that could aid in treatment and also predict the likelihood of recurrence of osteosarcoma in patients. Portland Press Ltd. 2020-01-06 /pmc/articles/PMC6944665/ /pubmed/31850493 http://dx.doi.org/10.1042/BSR20191251 Text en © 2020 The Author(s). https://creativecommons.org/licenses/by/4.0/ This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY).
spellingShingle Diagnostics & Biomarkers
Ying, Tang
Dong, Jin-ling
Yuan, Cen
Li, Peng
Guo, Qingshan
The lncRNAs RP1-261G23.7, RP11-69E11.4 and SATB2-AS1 are a novel clinical signature for predicting recurrent osteosarcoma
title The lncRNAs RP1-261G23.7, RP11-69E11.4 and SATB2-AS1 are a novel clinical signature for predicting recurrent osteosarcoma
title_full The lncRNAs RP1-261G23.7, RP11-69E11.4 and SATB2-AS1 are a novel clinical signature for predicting recurrent osteosarcoma
title_fullStr The lncRNAs RP1-261G23.7, RP11-69E11.4 and SATB2-AS1 are a novel clinical signature for predicting recurrent osteosarcoma
title_full_unstemmed The lncRNAs RP1-261G23.7, RP11-69E11.4 and SATB2-AS1 are a novel clinical signature for predicting recurrent osteosarcoma
title_short The lncRNAs RP1-261G23.7, RP11-69E11.4 and SATB2-AS1 are a novel clinical signature for predicting recurrent osteosarcoma
title_sort lncrnas rp1-261g23.7, rp11-69e11.4 and satb2-as1 are a novel clinical signature for predicting recurrent osteosarcoma
topic Diagnostics & Biomarkers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6944665/
https://www.ncbi.nlm.nih.gov/pubmed/31850493
http://dx.doi.org/10.1042/BSR20191251
work_keys_str_mv AT yingtang thelncrnasrp1261g237rp1169e114andsatb2as1areanovelclinicalsignatureforpredictingrecurrentosteosarcoma
AT dongjinling thelncrnasrp1261g237rp1169e114andsatb2as1areanovelclinicalsignatureforpredictingrecurrentosteosarcoma
AT yuancen thelncrnasrp1261g237rp1169e114andsatb2as1areanovelclinicalsignatureforpredictingrecurrentosteosarcoma
AT lipeng thelncrnasrp1261g237rp1169e114andsatb2as1areanovelclinicalsignatureforpredictingrecurrentosteosarcoma
AT guoqingshan thelncrnasrp1261g237rp1169e114andsatb2as1areanovelclinicalsignatureforpredictingrecurrentosteosarcoma
AT yingtang lncrnasrp1261g237rp1169e114andsatb2as1areanovelclinicalsignatureforpredictingrecurrentosteosarcoma
AT dongjinling lncrnasrp1261g237rp1169e114andsatb2as1areanovelclinicalsignatureforpredictingrecurrentosteosarcoma
AT yuancen lncrnasrp1261g237rp1169e114andsatb2as1areanovelclinicalsignatureforpredictingrecurrentosteosarcoma
AT lipeng lncrnasrp1261g237rp1169e114andsatb2as1areanovelclinicalsignatureforpredictingrecurrentosteosarcoma
AT guoqingshan lncrnasrp1261g237rp1169e114andsatb2as1areanovelclinicalsignatureforpredictingrecurrentosteosarcoma