Identification of the potential novel biomarkers as susceptibility gene for Wilms tumor
Abstract 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...
Main Authors: | , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2021-03-01
|
Series: | BMC Cancer |
Subjects: | |
Online Access: | https://doi.org/10.1186/s12885-021-08034-w |
id |
doaj-06bbd051e36b4a6fbe52e269f3fe3323 |
---|---|
record_format |
Article |
spelling |
doaj-06bbd051e36b4a6fbe52e269f3fe33232021-03-28T11:44:06ZengBMCBMC Cancer1471-24072021-03-0121111510.1186/s12885-021-08034-wIdentification of the potential novel biomarkers as susceptibility gene for Wilms tumorLi Liu0Zhe Song1Xu-Dong Gao2Xian Chen3Xiao-Bin Wu4Mi Wang5Yu-De Hong6Department of Urology, The Second Hospital, University of South ChinaDepartment of Urology, The Second Hospital, University of South ChinaCollege of Health Science and Nursing, Wuhan Polytechnic UniversityDepartment of Urology, The Second Hospital, University of South ChinaDepartment of Urology, The Second Hospital, University of South ChinaDepartment of Urology, The Second Hospital, University of South ChinaDepartment of Urology, The Second Hospital, University of South ChinaAbstract 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.https://doi.org/10.1186/s12885-021-08034-wWilms tumorBiomarkersRecurrenceOverall survival |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Li Liu Zhe Song Xu-Dong Gao Xian Chen Xiao-Bin Wu Mi Wang Yu-De Hong |
spellingShingle |
Li Liu Zhe Song Xu-Dong Gao Xian Chen Xiao-Bin Wu Mi Wang Yu-De Hong Identification of the potential novel biomarkers as susceptibility gene for Wilms tumor BMC Cancer Wilms tumor Biomarkers Recurrence Overall survival |
author_facet |
Li Liu Zhe Song Xu-Dong Gao Xian Chen Xiao-Bin Wu Mi Wang Yu-De Hong |
author_sort |
Li Liu |
title |
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_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_sort |
identification of the potential novel biomarkers as susceptibility gene for wilms tumor |
publisher |
BMC |
series |
BMC Cancer |
issn |
1471-2407 |
publishDate |
2021-03-01 |
description |
Abstract 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. |
topic |
Wilms tumor Biomarkers Recurrence Overall survival |
url |
https://doi.org/10.1186/s12885-021-08034-w |
work_keys_str_mv |
AT liliu identificationofthepotentialnovelbiomarkersassusceptibilitygeneforwilmstumor AT zhesong identificationofthepotentialnovelbiomarkersassusceptibilitygeneforwilmstumor AT xudonggao identificationofthepotentialnovelbiomarkersassusceptibilitygeneforwilmstumor AT xianchen identificationofthepotentialnovelbiomarkersassusceptibilitygeneforwilmstumor AT xiaobinwu identificationofthepotentialnovelbiomarkersassusceptibilitygeneforwilmstumor AT miwang identificationofthepotentialnovelbiomarkersassusceptibilitygeneforwilmstumor AT yudehong identificationofthepotentialnovelbiomarkersassusceptibilitygeneforwilmstumor |
_version_ |
1724199576283381760 |