Cargando…

Identification of a Two-Gene (PML-EPB41) Signature With Independent Prognostic Value in Osteosarcoma

Background: Osteosarcoma (OSA) is the most prevalent form of malignant bone cancer and it occurs predominantly in children and adolescents. OSA is associated with a poor prognosis and highest cause of cancer-related death. However, there are a few biomarkers that can serve as reasonable assessments...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Shengye, Liu, Jiamei, Yu, Xuechen, Shen, Tao, Fu, Qin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6992559/
https://www.ncbi.nlm.nih.gov/pubmed/32039036
http://dx.doi.org/10.3389/fonc.2019.01578
_version_ 1783492852753367040
author Liu, Shengye
Liu, Jiamei
Yu, Xuechen
Shen, Tao
Fu, Qin
author_facet Liu, Shengye
Liu, Jiamei
Yu, Xuechen
Shen, Tao
Fu, Qin
author_sort Liu, Shengye
collection PubMed
description Background: Osteosarcoma (OSA) is the most prevalent form of malignant bone cancer and it occurs predominantly in children and adolescents. OSA is associated with a poor prognosis and highest cause of cancer-related death. However, there are a few biomarkers that can serve as reasonable assessments of prognosis. Methods: Gene expression profiling data were downloaded from dataset GSE39058 and GSE21257 from the Gene Expression Omnibus database as well as TARGET database. Bioinformatic analysis with data integration was conducted to discover the significant biomarkers for predicting prognosis. Verification was conducted by qPCR and western blot to measure the expression of genes. Results: 733 seed genes were selected by combining the results of the expression profiling data with hub nodes in a human protein-protein interaction network with their gene functional enrichment categories identified. Following by Cox proportional risk regression modeling, a 2-gene (PML-EPB41) signature was developed for prognostic prediction of patients with OSA. Patients in the high-risk group had significantly poorer survival outcomes than in the low-risk group. Finally, the signature was validated and analyzed by the external dataset along with Kaplan–Meier survival analysis as well as biological experiment. A molecular gene model was built to serve as an innovative predictor of prognosis for patients with OSA. Conclusion: Our findings define novel biomarkers for OSA prognosis, which will possibly aid in the discovery of novel therapeutic targets with clinical applications.
format Online
Article
Text
id pubmed-6992559
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-69925592020-02-07 Identification of a Two-Gene (PML-EPB41) Signature With Independent Prognostic Value in Osteosarcoma Liu, Shengye Liu, Jiamei Yu, Xuechen Shen, Tao Fu, Qin Front Oncol Oncology Background: Osteosarcoma (OSA) is the most prevalent form of malignant bone cancer and it occurs predominantly in children and adolescents. OSA is associated with a poor prognosis and highest cause of cancer-related death. However, there are a few biomarkers that can serve as reasonable assessments of prognosis. Methods: Gene expression profiling data were downloaded from dataset GSE39058 and GSE21257 from the Gene Expression Omnibus database as well as TARGET database. Bioinformatic analysis with data integration was conducted to discover the significant biomarkers for predicting prognosis. Verification was conducted by qPCR and western blot to measure the expression of genes. Results: 733 seed genes were selected by combining the results of the expression profiling data with hub nodes in a human protein-protein interaction network with their gene functional enrichment categories identified. Following by Cox proportional risk regression modeling, a 2-gene (PML-EPB41) signature was developed for prognostic prediction of patients with OSA. Patients in the high-risk group had significantly poorer survival outcomes than in the low-risk group. Finally, the signature was validated and analyzed by the external dataset along with Kaplan–Meier survival analysis as well as biological experiment. A molecular gene model was built to serve as an innovative predictor of prognosis for patients with OSA. Conclusion: Our findings define novel biomarkers for OSA prognosis, which will possibly aid in the discovery of novel therapeutic targets with clinical applications. Frontiers Media S.A. 2020-01-24 /pmc/articles/PMC6992559/ /pubmed/32039036 http://dx.doi.org/10.3389/fonc.2019.01578 Text en Copyright © 2020 Liu, Liu, Yu, Shen and Fu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Liu, Shengye
Liu, Jiamei
Yu, Xuechen
Shen, Tao
Fu, Qin
Identification of a Two-Gene (PML-EPB41) Signature With Independent Prognostic Value in Osteosarcoma
title Identification of a Two-Gene (PML-EPB41) Signature With Independent Prognostic Value in Osteosarcoma
title_full Identification of a Two-Gene (PML-EPB41) Signature With Independent Prognostic Value in Osteosarcoma
title_fullStr Identification of a Two-Gene (PML-EPB41) Signature With Independent Prognostic Value in Osteosarcoma
title_full_unstemmed Identification of a Two-Gene (PML-EPB41) Signature With Independent Prognostic Value in Osteosarcoma
title_short Identification of a Two-Gene (PML-EPB41) Signature With Independent Prognostic Value in Osteosarcoma
title_sort identification of a two-gene (pml-epb41) signature with independent prognostic value in osteosarcoma
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6992559/
https://www.ncbi.nlm.nih.gov/pubmed/32039036
http://dx.doi.org/10.3389/fonc.2019.01578
work_keys_str_mv AT liushengye identificationofatwogenepmlepb41signaturewithindependentprognosticvalueinosteosarcoma
AT liujiamei identificationofatwogenepmlepb41signaturewithindependentprognosticvalueinosteosarcoma
AT yuxuechen identificationofatwogenepmlepb41signaturewithindependentprognosticvalueinosteosarcoma
AT shentao identificationofatwogenepmlepb41signaturewithindependentprognosticvalueinosteosarcoma
AT fuqin identificationofatwogenepmlepb41signaturewithindependentprognosticvalueinosteosarcoma