Construction and Validation of a Ferroptosis-Related Prognostic Model for Endometrial Cancer

Endometrial cancer (EC) is one of the most common female reproductive system tumors, with close to 200,000 new cases each year. It accounts for approximately 7% of the total number of female cancers, but until now the cause of EC has remained unclear. Ferroptosis is regulated cell death that disting...

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Main Authors: Hao Wang, Yingchen Wu, Shengfu Chen, Minzhi Hou, Yanning Yang, Meiqing Xie
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-09-01
Series:Frontiers in Genetics
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fgene.2021.729046/full
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spelling doaj-6720eb2531d54b9c919e3d746aad1b7b2021-09-28T06:10:29ZengFrontiers Media S.A.Frontiers in Genetics1664-80212021-09-011210.3389/fgene.2021.729046729046Construction and Validation of a Ferroptosis-Related Prognostic Model for Endometrial CancerHao WangYingchen WuShengfu ChenMinzhi HouYanning YangMeiqing XieEndometrial cancer (EC) is one of the most common female reproductive system tumors, with close to 200,000 new cases each year. It accounts for approximately 7% of the total number of female cancers, but until now the cause of EC has remained unclear. Ferroptosis is regulated cell death that distinguishes apoptosis and caused by oxidative damage. The process has unique biological effects on metabolism and redox biology. In this study, we analyzed the relationship between EC and ferroptosis. According to the different expression levels of related genes, we first divided 544 EC samples into four clusters and found that most of the infiltrating immune cells were significantly different among the four groups. A differential gene expression analysis between Fe.cluster groups was performed, and the samples were again divided into three Fe.gene.cluster groups. The molecular characteristics and clinical characteristics of the groups were significantly different. Finally, 13 characteristic genes were selected as ferroptosis gene signatures, and the Fe.score was obtained by calculation. The Fe.score is closely related to the clinical and molecular characteristics of EC, and a low Fe.score has a significant survival advantage. The GDSC predicts that the IC50 of multiple chemotherapeutic drugs is also significantly different between the two groups. In conclusion, our research has explored the relationship between EC and ferroptosis in detail, provides comprehensive insights for ferroptosis-mediated EC mechanism research, and emphasizes the clinical application potential of Fe.score-based immunotherapy strategies.https://www.frontiersin.org/articles/10.3389/fgene.2021.729046/fullferroptosisprognostic modelendometrial cancermolecular characteristicsclinical characteristics
collection DOAJ
language English
format Article
sources DOAJ
author Hao Wang
Yingchen Wu
Shengfu Chen
Minzhi Hou
Yanning Yang
Meiqing Xie
spellingShingle Hao Wang
Yingchen Wu
Shengfu Chen
Minzhi Hou
Yanning Yang
Meiqing Xie
Construction and Validation of a Ferroptosis-Related Prognostic Model for Endometrial Cancer
Frontiers in Genetics
ferroptosis
prognostic model
endometrial cancer
molecular characteristics
clinical characteristics
author_facet Hao Wang
Yingchen Wu
Shengfu Chen
Minzhi Hou
Yanning Yang
Meiqing Xie
author_sort Hao Wang
title Construction and Validation of a Ferroptosis-Related Prognostic Model for Endometrial Cancer
title_short Construction and Validation of a Ferroptosis-Related Prognostic Model for Endometrial Cancer
title_full Construction and Validation of a Ferroptosis-Related Prognostic Model for Endometrial Cancer
title_fullStr Construction and Validation of a Ferroptosis-Related Prognostic Model for Endometrial Cancer
title_full_unstemmed Construction and Validation of a Ferroptosis-Related Prognostic Model for Endometrial Cancer
title_sort construction and validation of a ferroptosis-related prognostic model for endometrial cancer
publisher Frontiers Media S.A.
series Frontiers in Genetics
issn 1664-8021
publishDate 2021-09-01
description Endometrial cancer (EC) is one of the most common female reproductive system tumors, with close to 200,000 new cases each year. It accounts for approximately 7% of the total number of female cancers, but until now the cause of EC has remained unclear. Ferroptosis is regulated cell death that distinguishes apoptosis and caused by oxidative damage. The process has unique biological effects on metabolism and redox biology. In this study, we analyzed the relationship between EC and ferroptosis. According to the different expression levels of related genes, we first divided 544 EC samples into four clusters and found that most of the infiltrating immune cells were significantly different among the four groups. A differential gene expression analysis between Fe.cluster groups was performed, and the samples were again divided into three Fe.gene.cluster groups. The molecular characteristics and clinical characteristics of the groups were significantly different. Finally, 13 characteristic genes were selected as ferroptosis gene signatures, and the Fe.score was obtained by calculation. The Fe.score is closely related to the clinical and molecular characteristics of EC, and a low Fe.score has a significant survival advantage. The GDSC predicts that the IC50 of multiple chemotherapeutic drugs is also significantly different between the two groups. In conclusion, our research has explored the relationship between EC and ferroptosis in detail, provides comprehensive insights for ferroptosis-mediated EC mechanism research, and emphasizes the clinical application potential of Fe.score-based immunotherapy strategies.
topic ferroptosis
prognostic model
endometrial cancer
molecular characteristics
clinical characteristics
url https://www.frontiersin.org/articles/10.3389/fgene.2021.729046/full
work_keys_str_mv AT haowang constructionandvalidationofaferroptosisrelatedprognosticmodelforendometrialcancer
AT yingchenwu constructionandvalidationofaferroptosisrelatedprognosticmodelforendometrialcancer
AT shengfuchen constructionandvalidationofaferroptosisrelatedprognosticmodelforendometrialcancer
AT minzhihou constructionandvalidationofaferroptosisrelatedprognosticmodelforendometrialcancer
AT yanningyang constructionandvalidationofaferroptosisrelatedprognosticmodelforendometrialcancer
AT meiqingxie constructionandvalidationofaferroptosisrelatedprognosticmodelforendometrialcancer
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