Comprehensive analysis of PLOD family members in low-grade gliomas using bioinformatics methods.

Low-grade gliomas (LGGs) is a primary invasive brain tumor that grows slowly but is incurable and eventually develops into high malignant glioma. Novel biomarkers for the tumorigenesis and lifetime of LGG are critically demanded to be investigated. In this study, the expression levels of procollagen...

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Main Authors: Yonghui Zhao, Xiang Zhang, Junchao Yao
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2021-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0246097
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spelling doaj-c9cd45247ffa4651a14f29f4f83955652021-06-25T04:31:34ZengPublic Library of Science (PLoS)PLoS ONE1932-62032021-01-01161e024609710.1371/journal.pone.0246097Comprehensive analysis of PLOD family members in low-grade gliomas using bioinformatics methods.Yonghui ZhaoXiang ZhangJunchao YaoLow-grade gliomas (LGGs) is a primary invasive brain tumor that grows slowly but is incurable and eventually develops into high malignant glioma. Novel biomarkers for the tumorigenesis and lifetime of LGG are critically demanded to be investigated. In this study, the expression levels of procollagen-lysine, 2-oxoglutarate 5-dioxygenases (PLODs) were analyzed by ONCOMINE, HPA and GEPIA. The GEPIA online platform was applied to evaluate the interrelation between PLODs and survival index in LGG. Furthermore, functions of PLODs and co-expression genes were inspected by the DAVID. Moreover, we used TIMER, cBioportal, GeneMINIA and NetworkAnalyst analysis to reveal the mechanism of PLODs in LGG. We found that expression levels of each PLOD family members were up-regulated in patients with LGG. Higher expression of PLODs was closely related to shorter disease-free survival (DFS) and overall survival (OS). The findings showed that LGG cases with or without alterations were significantly correlated with the OS and DFS. The mechanism of PLODs in LGG may be involved in response to hypoxia, oxidoreductase activity, Lysine degradation and immune cell infiltration. In general, this research has investigated the values of PLODs in LGG, which could serve as biomarkers for diagnosis, prognosis and potential therapeutic targets of LGG patients.https://doi.org/10.1371/journal.pone.0246097
collection DOAJ
language English
format Article
sources DOAJ
author Yonghui Zhao
Xiang Zhang
Junchao Yao
spellingShingle Yonghui Zhao
Xiang Zhang
Junchao Yao
Comprehensive analysis of PLOD family members in low-grade gliomas using bioinformatics methods.
PLoS ONE
author_facet Yonghui Zhao
Xiang Zhang
Junchao Yao
author_sort Yonghui Zhao
title Comprehensive analysis of PLOD family members in low-grade gliomas using bioinformatics methods.
title_short Comprehensive analysis of PLOD family members in low-grade gliomas using bioinformatics methods.
title_full Comprehensive analysis of PLOD family members in low-grade gliomas using bioinformatics methods.
title_fullStr Comprehensive analysis of PLOD family members in low-grade gliomas using bioinformatics methods.
title_full_unstemmed Comprehensive analysis of PLOD family members in low-grade gliomas using bioinformatics methods.
title_sort comprehensive analysis of plod family members in low-grade gliomas using bioinformatics methods.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2021-01-01
description Low-grade gliomas (LGGs) is a primary invasive brain tumor that grows slowly but is incurable and eventually develops into high malignant glioma. Novel biomarkers for the tumorigenesis and lifetime of LGG are critically demanded to be investigated. In this study, the expression levels of procollagen-lysine, 2-oxoglutarate 5-dioxygenases (PLODs) were analyzed by ONCOMINE, HPA and GEPIA. The GEPIA online platform was applied to evaluate the interrelation between PLODs and survival index in LGG. Furthermore, functions of PLODs and co-expression genes were inspected by the DAVID. Moreover, we used TIMER, cBioportal, GeneMINIA and NetworkAnalyst analysis to reveal the mechanism of PLODs in LGG. We found that expression levels of each PLOD family members were up-regulated in patients with LGG. Higher expression of PLODs was closely related to shorter disease-free survival (DFS) and overall survival (OS). The findings showed that LGG cases with or without alterations were significantly correlated with the OS and DFS. The mechanism of PLODs in LGG may be involved in response to hypoxia, oxidoreductase activity, Lysine degradation and immune cell infiltration. In general, this research has investigated the values of PLODs in LGG, which could serve as biomarkers for diagnosis, prognosis and potential therapeutic targets of LGG patients.
url https://doi.org/10.1371/journal.pone.0246097
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