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Molecular and clinical characterization of PTRF in glioma via 1,022 samples
Polymerase I and transcript release factor (PTRF) plays a role in the regulation of gene expression and the release of RNA transcripts during transcription, which have been associated with various human diseases. However, the role of PTRF in glioma remains unclear. In this study, RNA sequencing (RNA...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10273567/ https://www.ncbi.nlm.nih.gov/pubmed/37322408 http://dx.doi.org/10.1186/s12885-023-11001-2 |
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author | Sun, Si Yang, Changlin Wang, Kuanyu Huang, Ruoyu Zhang, Ke-nan Liu, Yanwei Cao, Zhi Zhao, Zheng Jiang, Tao |
author_facet | Sun, Si Yang, Changlin Wang, Kuanyu Huang, Ruoyu Zhang, Ke-nan Liu, Yanwei Cao, Zhi Zhao, Zheng Jiang, Tao |
author_sort | Sun, Si |
collection | PubMed |
description | Polymerase I and transcript release factor (PTRF) plays a role in the regulation of gene expression and the release of RNA transcripts during transcription, which have been associated with various human diseases. However, the role of PTRF in glioma remains unclear. In this study, RNA sequencing (RNA-seq) data (n = 1022 cases) and whole-exome sequencing (WES) data (n = 286 cases) were used to characterize the PTRF expression features. Gene ontology (GO) functional enrichment analysis was used to assess the biological implication of changes in PTRF expression. As a result, the expression of PTRF was associated with malignant progression in gliomas. Meanwhile, somatic mutational profiles and copy number variations (CNV) revealed the glioma subtypes classified by PTRF expression showed distinct genomic alteration. Furthermore, GO functional enrichment analysis suggested that PTRF expression was associated with cell migration and angiogenesis, particularly during an immune response. Survival analysis confirmed that a high expression of PTRF is associated with a poor prognosis. In summary, PTRF may be a valuable factor for the diagnosis and treatment target of glioma. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-023-11001-2. |
format | Online Article Text |
id | pubmed-10273567 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-102735672023-06-17 Molecular and clinical characterization of PTRF in glioma via 1,022 samples Sun, Si Yang, Changlin Wang, Kuanyu Huang, Ruoyu Zhang, Ke-nan Liu, Yanwei Cao, Zhi Zhao, Zheng Jiang, Tao BMC Cancer Research Polymerase I and transcript release factor (PTRF) plays a role in the regulation of gene expression and the release of RNA transcripts during transcription, which have been associated with various human diseases. However, the role of PTRF in glioma remains unclear. In this study, RNA sequencing (RNA-seq) data (n = 1022 cases) and whole-exome sequencing (WES) data (n = 286 cases) were used to characterize the PTRF expression features. Gene ontology (GO) functional enrichment analysis was used to assess the biological implication of changes in PTRF expression. As a result, the expression of PTRF was associated with malignant progression in gliomas. Meanwhile, somatic mutational profiles and copy number variations (CNV) revealed the glioma subtypes classified by PTRF expression showed distinct genomic alteration. Furthermore, GO functional enrichment analysis suggested that PTRF expression was associated with cell migration and angiogenesis, particularly during an immune response. Survival analysis confirmed that a high expression of PTRF is associated with a poor prognosis. In summary, PTRF may be a valuable factor for the diagnosis and treatment target of glioma. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-023-11001-2. BioMed Central 2023-06-16 /pmc/articles/PMC10273567/ /pubmed/37322408 http://dx.doi.org/10.1186/s12885-023-11001-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Sun, Si Yang, Changlin Wang, Kuanyu Huang, Ruoyu Zhang, Ke-nan Liu, Yanwei Cao, Zhi Zhao, Zheng Jiang, Tao Molecular and clinical characterization of PTRF in glioma via 1,022 samples |
title | Molecular and clinical characterization of PTRF in glioma via 1,022 samples |
title_full | Molecular and clinical characterization of PTRF in glioma via 1,022 samples |
title_fullStr | Molecular and clinical characterization of PTRF in glioma via 1,022 samples |
title_full_unstemmed | Molecular and clinical characterization of PTRF in glioma via 1,022 samples |
title_short | Molecular and clinical characterization of PTRF in glioma via 1,022 samples |
title_sort | molecular and clinical characterization of ptrf in glioma via 1,022 samples |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10273567/ https://www.ncbi.nlm.nih.gov/pubmed/37322408 http://dx.doi.org/10.1186/s12885-023-11001-2 |
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