Multi-omics landscape of circadian rhythm pathway alterations in Glioma

Circadian rhythm pathway was demonstrated pathological functions in glioma on single-gene level. We aim to depict the multi-omics landscape of circadian rhythm pathway alteration in glioma using bioinformatic analyses. Multi-omics data were obtained from “cBioPortal” database. Comparisons were done...

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Main Authors: Chang Zhang, Jiahui Xu, Lijun Chen, Xiaojie Lin
Format: Article
Language:English
Published: Taylor & Francis Group 2021-01-01
Series:Bioengineered
Subjects:
Online Access:http://dx.doi.org/10.1080/21655979.2021.1947075
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spelling doaj-7fab7a590afa469fabeb3316a50b78212021-07-06T12:16:11ZengTaylor & Francis GroupBioengineered2165-59792165-59872021-01-011213294330810.1080/21655979.2021.19470751947075Multi-omics landscape of circadian rhythm pathway alterations in GliomaChang Zhang0Jiahui Xu1Lijun Chen2Xiaojie Lin3Guang Dong Second Hospital of Traditional Chinese MedicineGuang Dong Second Hospital of Traditional Chinese MedicineThe Fifth Clinical College of Guangzhou University of Chinese MedicineGuang Dong Second Hospital of Traditional Chinese MedicineCircadian rhythm pathway was demonstrated pathological functions in glioma on single-gene level. We aim to depict the multi-omics landscape of circadian rhythm pathway alteration in glioma using bioinformatic analyses. Multi-omics data were obtained from “cBioPortal” database. Comparisons were done regarding clinical parameters, differential-expressed genes and functional annotations. A pathway index was generated using the expression data from TCGA and GTEx to quantify the general alteration level of the pathway with clinical association of circadian rhythm pathway index explored. A total of 30 genes were mapped on the circadian rhythm pathway. Genomic profile ofcircadian rhythm pathway genes exhibited distinct characteristics on multiple levels between lower grade glioma (LGG) and glioblastoma multiforme (GBM) patients. LGG patients presented significantly higher frequencies of multi-omics mutations, as well as significant clinical relevance, on single-gene level. Differential-expressed genes between LGG and GBM patients revealed different functions between subtypes that related to the alteration of circadian rhythm pathway. LGG have significantly higher pathway index than normal brain tissue, while GBM significantly lower than normal tissue (P < 0.01), indicating distinctly altered circadian pathway in LGG. Circadian rhythm pathway index correlated with the prognosis of LGG, but not GBM, patients, with higher score indicating better survival outcome (LGG: HR = 0.39, 95% CI: 0.26 − 0.59, P < 0.001). In conclusion, LGG have more multi-omics alterations of circadian rhythm pathway than GBM. Quantification of circadian rhythm pathway using pathway index demonstrated hyperactivated pathway status in LGG and correlated with the prognosis of LGG patients.http://dx.doi.org/10.1080/21655979.2021.1947075circadian rhythmprognostic biomarkermulti-omicsbioinformatic analysis
collection DOAJ
language English
format Article
sources DOAJ
author Chang Zhang
Jiahui Xu
Lijun Chen
Xiaojie Lin
spellingShingle Chang Zhang
Jiahui Xu
Lijun Chen
Xiaojie Lin
Multi-omics landscape of circadian rhythm pathway alterations in Glioma
Bioengineered
circadian rhythm
prognostic biomarker
multi-omics
bioinformatic analysis
author_facet Chang Zhang
Jiahui Xu
Lijun Chen
Xiaojie Lin
author_sort Chang Zhang
title Multi-omics landscape of circadian rhythm pathway alterations in Glioma
title_short Multi-omics landscape of circadian rhythm pathway alterations in Glioma
title_full Multi-omics landscape of circadian rhythm pathway alterations in Glioma
title_fullStr Multi-omics landscape of circadian rhythm pathway alterations in Glioma
title_full_unstemmed Multi-omics landscape of circadian rhythm pathway alterations in Glioma
title_sort multi-omics landscape of circadian rhythm pathway alterations in glioma
publisher Taylor & Francis Group
series Bioengineered
issn 2165-5979
2165-5987
publishDate 2021-01-01
description Circadian rhythm pathway was demonstrated pathological functions in glioma on single-gene level. We aim to depict the multi-omics landscape of circadian rhythm pathway alteration in glioma using bioinformatic analyses. Multi-omics data were obtained from “cBioPortal” database. Comparisons were done regarding clinical parameters, differential-expressed genes and functional annotations. A pathway index was generated using the expression data from TCGA and GTEx to quantify the general alteration level of the pathway with clinical association of circadian rhythm pathway index explored. A total of 30 genes were mapped on the circadian rhythm pathway. Genomic profile ofcircadian rhythm pathway genes exhibited distinct characteristics on multiple levels between lower grade glioma (LGG) and glioblastoma multiforme (GBM) patients. LGG patients presented significantly higher frequencies of multi-omics mutations, as well as significant clinical relevance, on single-gene level. Differential-expressed genes between LGG and GBM patients revealed different functions between subtypes that related to the alteration of circadian rhythm pathway. LGG have significantly higher pathway index than normal brain tissue, while GBM significantly lower than normal tissue (P < 0.01), indicating distinctly altered circadian pathway in LGG. Circadian rhythm pathway index correlated with the prognosis of LGG, but not GBM, patients, with higher score indicating better survival outcome (LGG: HR = 0.39, 95% CI: 0.26 − 0.59, P < 0.001). In conclusion, LGG have more multi-omics alterations of circadian rhythm pathway than GBM. Quantification of circadian rhythm pathway using pathway index demonstrated hyperactivated pathway status in LGG and correlated with the prognosis of LGG patients.
topic circadian rhythm
prognostic biomarker
multi-omics
bioinformatic analysis
url http://dx.doi.org/10.1080/21655979.2021.1947075
work_keys_str_mv AT changzhang multiomicslandscapeofcircadianrhythmpathwayalterationsinglioma
AT jiahuixu multiomicslandscapeofcircadianrhythmpathwayalterationsinglioma
AT lijunchen multiomicslandscapeofcircadianrhythmpathwayalterationsinglioma
AT xiaojielin multiomicslandscapeofcircadianrhythmpathwayalterationsinglioma
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