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Identification of a novel MYC target gene set signature for predicting the prognosis of osteosarcoma patients

Osteosarcoma is a primary malignant tumor found mainly in teenagers and young adults. Patients have very little long-term survival. MYC controls tumor initiation and progression by regulating the expression of its target genes; thus, constructing a risk signature of osteosarcoma MYC target gene set...

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Autores principales: Gong, Deliang, Zhao, Qingzhong, Liu, Jun, Zhao, Shibing, Yi, Chengfeng, Lv, Jianwei, Yu, Hang, Bian, Erbao, Tian, Dasheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10277635/
https://www.ncbi.nlm.nih.gov/pubmed/37342196
http://dx.doi.org/10.3389/fonc.2023.1169430
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author Gong, Deliang
Zhao, Qingzhong
Liu, Jun
Zhao, Shibing
Yi, Chengfeng
Lv, Jianwei
Yu, Hang
Bian, Erbao
Tian, Dasheng
author_facet Gong, Deliang
Zhao, Qingzhong
Liu, Jun
Zhao, Shibing
Yi, Chengfeng
Lv, Jianwei
Yu, Hang
Bian, Erbao
Tian, Dasheng
author_sort Gong, Deliang
collection PubMed
description Osteosarcoma is a primary malignant tumor found mainly in teenagers and young adults. Patients have very little long-term survival. MYC controls tumor initiation and progression by regulating the expression of its target genes; thus, constructing a risk signature of osteosarcoma MYC target gene set will benefit the evaluation of both treatment and prognosis. In this paper, we used GEO data to download the ChIP-seq data of MYC to obtain the MYC target gene. Then, a risk signature consisting of 10 MYC target genes was developed using Cox regression analysis. The signature indicates that patients in the high-risk group performed poorly. After that, we verified it in the GSE21257 dataset. In addition, the difference in tumor immune function among the low- and high-risk populations was compared by single sample gene enrichment analysis. Immunotherapy and prediction of response to the anticancer drug have shown that the risk signature of the MYC target gene set was positively correlated with immune checkpoint response and drug sensitivity. Functional analysis has demonstrated that these genes are enriched in malignant tumors. Finally, STX10 was selected for functional experimentation. STX10 silence has limited osteosarcoma cell migration, invasion, and proliferation. Therefore, these findings indicated that the MYC target gene set risk signature could be used as a potential therapeutic target and prognostic indicator in patients with osteosarcoma.
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spelling pubmed-102776352023-06-20 Identification of a novel MYC target gene set signature for predicting the prognosis of osteosarcoma patients Gong, Deliang Zhao, Qingzhong Liu, Jun Zhao, Shibing Yi, Chengfeng Lv, Jianwei Yu, Hang Bian, Erbao Tian, Dasheng Front Oncol Oncology Osteosarcoma is a primary malignant tumor found mainly in teenagers and young adults. Patients have very little long-term survival. MYC controls tumor initiation and progression by regulating the expression of its target genes; thus, constructing a risk signature of osteosarcoma MYC target gene set will benefit the evaluation of both treatment and prognosis. In this paper, we used GEO data to download the ChIP-seq data of MYC to obtain the MYC target gene. Then, a risk signature consisting of 10 MYC target genes was developed using Cox regression analysis. The signature indicates that patients in the high-risk group performed poorly. After that, we verified it in the GSE21257 dataset. In addition, the difference in tumor immune function among the low- and high-risk populations was compared by single sample gene enrichment analysis. Immunotherapy and prediction of response to the anticancer drug have shown that the risk signature of the MYC target gene set was positively correlated with immune checkpoint response and drug sensitivity. Functional analysis has demonstrated that these genes are enriched in malignant tumors. Finally, STX10 was selected for functional experimentation. STX10 silence has limited osteosarcoma cell migration, invasion, and proliferation. Therefore, these findings indicated that the MYC target gene set risk signature could be used as a potential therapeutic target and prognostic indicator in patients with osteosarcoma. Frontiers Media S.A. 2023-06-05 /pmc/articles/PMC10277635/ /pubmed/37342196 http://dx.doi.org/10.3389/fonc.2023.1169430 Text en Copyright © 2023 Gong, Zhao, Liu, Zhao, Yi, Lv, Yu, Bian and Tian 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
Gong, Deliang
Zhao, Qingzhong
Liu, Jun
Zhao, Shibing
Yi, Chengfeng
Lv, Jianwei
Yu, Hang
Bian, Erbao
Tian, Dasheng
Identification of a novel MYC target gene set signature for predicting the prognosis of osteosarcoma patients
title Identification of a novel MYC target gene set signature for predicting the prognosis of osteosarcoma patients
title_full Identification of a novel MYC target gene set signature for predicting the prognosis of osteosarcoma patients
title_fullStr Identification of a novel MYC target gene set signature for predicting the prognosis of osteosarcoma patients
title_full_unstemmed Identification of a novel MYC target gene set signature for predicting the prognosis of osteosarcoma patients
title_short Identification of a novel MYC target gene set signature for predicting the prognosis of osteosarcoma patients
title_sort identification of a novel myc target gene set signature for predicting the prognosis of osteosarcoma patients
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10277635/
https://www.ncbi.nlm.nih.gov/pubmed/37342196
http://dx.doi.org/10.3389/fonc.2023.1169430
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