Gene biomarker prediction in glioma by integrating scRNA-seq data and gene regulatory network

Abstract Background Although great efforts have been made to study the occurrence and development of glioma, the molecular mechanisms of glioma are still unclear. Single-cell sequencing technology provides a new perspective for researchers to explore the pathogens of tumors to further help make trea...

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Autores principales: Guimin Qin, Longting Du, Yuying Ma, Yu Yin, Liming Wang
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Lenguaje:EN
Publicado: BMC 2021
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Acceso en línea:https://doaj.org/article/a0ffd114be374eaa813f6e766b708cfa
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spelling oai:doaj.org-article:a0ffd114be374eaa813f6e766b708cfa2021-12-05T12:05:25ZGene biomarker prediction in glioma by integrating scRNA-seq data and gene regulatory network10.1186/s12920-021-01115-61755-8794https://doaj.org/article/a0ffd114be374eaa813f6e766b708cfa2021-12-01T00:00:00Zhttps://doi.org/10.1186/s12920-021-01115-6https://doaj.org/toc/1755-8794Abstract Background Although great efforts have been made to study the occurrence and development of glioma, the molecular mechanisms of glioma are still unclear. Single-cell sequencing technology provides a new perspective for researchers to explore the pathogens of tumors to further help make treatment and prognosis decisions for patients with tumors. Methods In this study, we proposed an algorithm framework to explore the molecular mechanisms of glioma by integrating single-cell gene expression profiles and gene regulatory relations. First, since there were great differences among malignant cells from different glioma samples, we analyzed the expression status of malignant cells for each sample, and then tumor consensus genes were identified by constructing and analyzing cell-specific networks. Second, to comprehensively analyze the characteristics of glioma, we integrated transcriptional regulatory relationships and consensus genes to construct a tumor-specific regulatory network. Third, we performed a hybrid clustering analysis to identify glioma cell types. Finally, candidate tumor gene biomarkers were identified based on cell types and known glioma-related genes. Results We got six identified cell types using the method we proposed and for these cell types, we performed functional and biological pathway enrichment analyses. The candidate tumor gene biomarkers were analyzed through survival analysis and verified using literature from PubMed. Conclusions The results showed that these candidate tumor gene biomarkers were closely related to glioma and could provide clues for the diagnosis and prognosis of patients with glioma. In addition, we found that four of the candidate tumor gene biomarkers (NDUFS5, NDUFA1, NDUFA13, and NDUFB8) belong to the NADH ubiquinone oxidoreductase subunit gene family, so we inferred that this gene family may be strongly related to glioma.Guimin QinLongting DuYuying MaYu YinLiming WangBMCarticleGliomaSingle-cell gene expression profileCell typeTumor gene biomarkersInternal medicineRC31-1245GeneticsQH426-470ENBMC Medical Genomics, Vol 14, Iss 1, Pp 1-13 (2021)
institution DOAJ
collection DOAJ
language EN
topic Glioma
Single-cell gene expression profile
Cell type
Tumor gene biomarkers
Internal medicine
RC31-1245
Genetics
QH426-470
spellingShingle Glioma
Single-cell gene expression profile
Cell type
Tumor gene biomarkers
Internal medicine
RC31-1245
Genetics
QH426-470
Guimin Qin
Longting Du
Yuying Ma
Yu Yin
Liming Wang
Gene biomarker prediction in glioma by integrating scRNA-seq data and gene regulatory network
description Abstract Background Although great efforts have been made to study the occurrence and development of glioma, the molecular mechanisms of glioma are still unclear. Single-cell sequencing technology provides a new perspective for researchers to explore the pathogens of tumors to further help make treatment and prognosis decisions for patients with tumors. Methods In this study, we proposed an algorithm framework to explore the molecular mechanisms of glioma by integrating single-cell gene expression profiles and gene regulatory relations. First, since there were great differences among malignant cells from different glioma samples, we analyzed the expression status of malignant cells for each sample, and then tumor consensus genes were identified by constructing and analyzing cell-specific networks. Second, to comprehensively analyze the characteristics of glioma, we integrated transcriptional regulatory relationships and consensus genes to construct a tumor-specific regulatory network. Third, we performed a hybrid clustering analysis to identify glioma cell types. Finally, candidate tumor gene biomarkers were identified based on cell types and known glioma-related genes. Results We got six identified cell types using the method we proposed and for these cell types, we performed functional and biological pathway enrichment analyses. The candidate tumor gene biomarkers were analyzed through survival analysis and verified using literature from PubMed. Conclusions The results showed that these candidate tumor gene biomarkers were closely related to glioma and could provide clues for the diagnosis and prognosis of patients with glioma. In addition, we found that four of the candidate tumor gene biomarkers (NDUFS5, NDUFA1, NDUFA13, and NDUFB8) belong to the NADH ubiquinone oxidoreductase subunit gene family, so we inferred that this gene family may be strongly related to glioma.
format article
author Guimin Qin
Longting Du
Yuying Ma
Yu Yin
Liming Wang
author_facet Guimin Qin
Longting Du
Yuying Ma
Yu Yin
Liming Wang
author_sort Guimin Qin
title Gene biomarker prediction in glioma by integrating scRNA-seq data and gene regulatory network
title_short Gene biomarker prediction in glioma by integrating scRNA-seq data and gene regulatory network
title_full Gene biomarker prediction in glioma by integrating scRNA-seq data and gene regulatory network
title_fullStr Gene biomarker prediction in glioma by integrating scRNA-seq data and gene regulatory network
title_full_unstemmed Gene biomarker prediction in glioma by integrating scRNA-seq data and gene regulatory network
title_sort gene biomarker prediction in glioma by integrating scrna-seq data and gene regulatory network
publisher BMC
publishDate 2021
url https://doaj.org/article/a0ffd114be374eaa813f6e766b708cfa
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AT longtingdu genebiomarkerpredictioningliomabyintegratingscrnaseqdataandgeneregulatorynetwork
AT yuyingma genebiomarkerpredictioningliomabyintegratingscrnaseqdataandgeneregulatorynetwork
AT yuyin genebiomarkerpredictioningliomabyintegratingscrnaseqdataandgeneregulatorynetwork
AT limingwang genebiomarkerpredictioningliomabyintegratingscrnaseqdataandgeneregulatorynetwork
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