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Identification of the potential novel biomarkers as susceptibility gene for Wilms tumor

BACKGROUND: Wilms tumor (WT) is the most common malignant renal tumor in children. The aim of this study was to identify potential susceptibility gene of WT for better prognosis. METHODS: Weighted gene coexpression network analysis is used for the detection of clinically important biomarkers associa...

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Autores principales: Liu, Li, Song, Zhe, Gao, Xu-Dong, Chen, Xian, Wu, Xiao-Bin, Wang, Mi, Hong, Yu-De
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7992941/
https://www.ncbi.nlm.nih.gov/pubmed/33765954
http://dx.doi.org/10.1186/s12885-021-08034-w
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author Liu, Li
Song, Zhe
Gao, Xu-Dong
Chen, Xian
Wu, Xiao-Bin
Wang, Mi
Hong, Yu-De
author_facet Liu, Li
Song, Zhe
Gao, Xu-Dong
Chen, Xian
Wu, Xiao-Bin
Wang, Mi
Hong, Yu-De
author_sort Liu, Li
collection PubMed
description BACKGROUND: Wilms tumor (WT) is the most common malignant renal tumor in children. The aim of this study was to identify potential susceptibility gene of WT for better prognosis. METHODS: Weighted gene coexpression network analysis is used for the detection of clinically important biomarkers associated with WT. RESULTS: In the study, 59 tissue samples from National Cancer Institute were pretreated for constructing gene co-expression network, while 224 samples also downloaded from National Cancer Institute were used for hub gene validation and module preservation analysis. Three modules were found to be highly correlated with WT, and 44 top hub genes were identified in these key modules eventually. In addition, both the module preservation analysis and gene validation showed ideal results based on other dataset with 224 samples. Meanwhile, Functional enrichment analysis showed that genes in module were enriched to sister chromatid cohesion, cell cycle, oocyte meiosis. CONCLUSION: In summary, we established a gene co-expression network to identify 44 hub genes are closely to recurrence and staging of WT, and 6 of these hub genes was closely related to the poor prognosis of patients. Our findings revealed that those hub genes may be used as potential susceptibility gene for clinical diagnosis and prognosis of this tumor. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-021-08034-w.
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spelling pubmed-79929412021-03-25 Identification of the potential novel biomarkers as susceptibility gene for Wilms tumor Liu, Li Song, Zhe Gao, Xu-Dong Chen, Xian Wu, Xiao-Bin Wang, Mi Hong, Yu-De BMC Cancer Research Article BACKGROUND: Wilms tumor (WT) is the most common malignant renal tumor in children. The aim of this study was to identify potential susceptibility gene of WT for better prognosis. METHODS: Weighted gene coexpression network analysis is used for the detection of clinically important biomarkers associated with WT. RESULTS: In the study, 59 tissue samples from National Cancer Institute were pretreated for constructing gene co-expression network, while 224 samples also downloaded from National Cancer Institute were used for hub gene validation and module preservation analysis. Three modules were found to be highly correlated with WT, and 44 top hub genes were identified in these key modules eventually. In addition, both the module preservation analysis and gene validation showed ideal results based on other dataset with 224 samples. Meanwhile, Functional enrichment analysis showed that genes in module were enriched to sister chromatid cohesion, cell cycle, oocyte meiosis. CONCLUSION: In summary, we established a gene co-expression network to identify 44 hub genes are closely to recurrence and staging of WT, and 6 of these hub genes was closely related to the poor prognosis of patients. Our findings revealed that those hub genes may be used as potential susceptibility gene for clinical diagnosis and prognosis of this tumor. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-021-08034-w. BioMed Central 2021-03-25 /pmc/articles/PMC7992941/ /pubmed/33765954 http://dx.doi.org/10.1186/s12885-021-08034-w Text en © The Author(s) 2021 Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://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 Article
Liu, Li
Song, Zhe
Gao, Xu-Dong
Chen, Xian
Wu, Xiao-Bin
Wang, Mi
Hong, Yu-De
Identification of the potential novel biomarkers as susceptibility gene for Wilms tumor
title Identification of the potential novel biomarkers as susceptibility gene for Wilms tumor
title_full Identification of the potential novel biomarkers as susceptibility gene for Wilms tumor
title_fullStr Identification of the potential novel biomarkers as susceptibility gene for Wilms tumor
title_full_unstemmed Identification of the potential novel biomarkers as susceptibility gene for Wilms tumor
title_short Identification of the potential novel biomarkers as susceptibility gene for Wilms tumor
title_sort identification of the potential novel biomarkers as susceptibility gene for wilms tumor
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7992941/
https://www.ncbi.nlm.nih.gov/pubmed/33765954
http://dx.doi.org/10.1186/s12885-021-08034-w
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