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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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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 |
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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 |
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