Cargando…

A novel prognostic related lncRNA signature associated with amino acid metabolism in glioma

BACKGROUND: Glioma is one of the deadliest malignant brain tumors in adults, which is highly invasive and has a poor prognosis, and long non-coding RNAs (lncRNAs) have key roles in the progression of glioma. Amino acid metabolism reprogramming is an emerging hallmark in cancer. However, the diverse...

Descripción completa

Detalles Bibliográficos
Autores principales: Lei, Qiang, Yuan, Bo, Liu, Kun, Peng, Li, Xia, Zhiwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10126287/
https://www.ncbi.nlm.nih.gov/pubmed/37114036
http://dx.doi.org/10.3389/fimmu.2023.1014378
_version_ 1785030207878463488
author Lei, Qiang
Yuan, Bo
Liu, Kun
Peng, Li
Xia, Zhiwei
author_facet Lei, Qiang
Yuan, Bo
Liu, Kun
Peng, Li
Xia, Zhiwei
author_sort Lei, Qiang
collection PubMed
description BACKGROUND: Glioma is one of the deadliest malignant brain tumors in adults, which is highly invasive and has a poor prognosis, and long non-coding RNAs (lncRNAs) have key roles in the progression of glioma. Amino acid metabolism reprogramming is an emerging hallmark in cancer. However, the diverse amino acid metabolism programs and prognostic value remain unclear during glioma progression. Thus, we aim to find potential amino-related prognostic glioma hub genes, elaborate and verify their functions, and explore further their impact on glioma. METHODS: Glioblastoma (GBM) and low-grade glioma (LGG) patients’ data were downloaded from TCGA and CCGA datasets. LncRNAs associated with amino acid metabolism were discriminated against via correlation analysis. LASSO analysis and Cox regression analysis were conducted to identify lncRNAs related to prognosis. GSVA and GSEA were performed to predict the potential biological functions of lncRNA. Somatic mutation data and CNV data were further built to demonstrate genomic alterations and the correlation between risk scores. Human glioma cell lines U251 and U87-MG were used for further validation in vitro experiments. RESULTS: There were eight amino-related lncRNAs in total with a high prognostic value that were identified via Cox regression and LASSO regression analyses. The high risk-score group presented a significantly poorer prognosis compared with the low risk-score group, with more clinicopathological features and characteristic genomic aberrations. Our results provided new insights into biological functions in the above signature lncRNAs, which participate in the amino acid metabolism of glioma. LINC01561 is one of the eight identified lncRNAs, which was adopted for further verification. In in vitro experiments, siRNA-mediated LINC01561 silencing suppresses glioma cells’ viability, migration, and proliferation. CONCLUSION: Novel amino-related lncRNAs associated with the survival of glioma patients were identified, and a lncRNA signature can predict glioma prognosis and therapy response, which possibly has vital roles in glioma. Meanwhile, it emphasized the importance of amino acid metabolism in glioma, particularly in providing deeper research at the molecular level.
format Online
Article
Text
id pubmed-10126287
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-101262872023-04-26 A novel prognostic related lncRNA signature associated with amino acid metabolism in glioma Lei, Qiang Yuan, Bo Liu, Kun Peng, Li Xia, Zhiwei Front Immunol Immunology BACKGROUND: Glioma is one of the deadliest malignant brain tumors in adults, which is highly invasive and has a poor prognosis, and long non-coding RNAs (lncRNAs) have key roles in the progression of glioma. Amino acid metabolism reprogramming is an emerging hallmark in cancer. However, the diverse amino acid metabolism programs and prognostic value remain unclear during glioma progression. Thus, we aim to find potential amino-related prognostic glioma hub genes, elaborate and verify their functions, and explore further their impact on glioma. METHODS: Glioblastoma (GBM) and low-grade glioma (LGG) patients’ data were downloaded from TCGA and CCGA datasets. LncRNAs associated with amino acid metabolism were discriminated against via correlation analysis. LASSO analysis and Cox regression analysis were conducted to identify lncRNAs related to prognosis. GSVA and GSEA were performed to predict the potential biological functions of lncRNA. Somatic mutation data and CNV data were further built to demonstrate genomic alterations and the correlation between risk scores. Human glioma cell lines U251 and U87-MG were used for further validation in vitro experiments. RESULTS: There were eight amino-related lncRNAs in total with a high prognostic value that were identified via Cox regression and LASSO regression analyses. The high risk-score group presented a significantly poorer prognosis compared with the low risk-score group, with more clinicopathological features and characteristic genomic aberrations. Our results provided new insights into biological functions in the above signature lncRNAs, which participate in the amino acid metabolism of glioma. LINC01561 is one of the eight identified lncRNAs, which was adopted for further verification. In in vitro experiments, siRNA-mediated LINC01561 silencing suppresses glioma cells’ viability, migration, and proliferation. CONCLUSION: Novel amino-related lncRNAs associated with the survival of glioma patients were identified, and a lncRNA signature can predict glioma prognosis and therapy response, which possibly has vital roles in glioma. Meanwhile, it emphasized the importance of amino acid metabolism in glioma, particularly in providing deeper research at the molecular level. Frontiers Media S.A. 2023-04-11 /pmc/articles/PMC10126287/ /pubmed/37114036 http://dx.doi.org/10.3389/fimmu.2023.1014378 Text en Copyright © 2023 Lei, Yuan, Liu, Peng and Xia 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 Immunology
Lei, Qiang
Yuan, Bo
Liu, Kun
Peng, Li
Xia, Zhiwei
A novel prognostic related lncRNA signature associated with amino acid metabolism in glioma
title A novel prognostic related lncRNA signature associated with amino acid metabolism in glioma
title_full A novel prognostic related lncRNA signature associated with amino acid metabolism in glioma
title_fullStr A novel prognostic related lncRNA signature associated with amino acid metabolism in glioma
title_full_unstemmed A novel prognostic related lncRNA signature associated with amino acid metabolism in glioma
title_short A novel prognostic related lncRNA signature associated with amino acid metabolism in glioma
title_sort novel prognostic related lncrna signature associated with amino acid metabolism in glioma
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10126287/
https://www.ncbi.nlm.nih.gov/pubmed/37114036
http://dx.doi.org/10.3389/fimmu.2023.1014378
work_keys_str_mv AT leiqiang anovelprognosticrelatedlncrnasignatureassociatedwithaminoacidmetabolisminglioma
AT yuanbo anovelprognosticrelatedlncrnasignatureassociatedwithaminoacidmetabolisminglioma
AT liukun anovelprognosticrelatedlncrnasignatureassociatedwithaminoacidmetabolisminglioma
AT pengli anovelprognosticrelatedlncrnasignatureassociatedwithaminoacidmetabolisminglioma
AT xiazhiwei anovelprognosticrelatedlncrnasignatureassociatedwithaminoacidmetabolisminglioma
AT leiqiang novelprognosticrelatedlncrnasignatureassociatedwithaminoacidmetabolisminglioma
AT yuanbo novelprognosticrelatedlncrnasignatureassociatedwithaminoacidmetabolisminglioma
AT liukun novelprognosticrelatedlncrnasignatureassociatedwithaminoacidmetabolisminglioma
AT pengli novelprognosticrelatedlncrnasignatureassociatedwithaminoacidmetabolisminglioma
AT xiazhiwei novelprognosticrelatedlncrnasignatureassociatedwithaminoacidmetabolisminglioma