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Analysis and prediction model of ferroptosis related genes in breast cancer

BACKGROUND: The prognosis of patients with breast cancer (BRCA) is difficult to predict because of the high degree of heterogeneity and complex etiological factors. Ferroptosis, an iron-dependent, new form of cell death, plays an important role in regulation of tumor growth and progression. The aim...

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Autores principales: Wang, Lingli, Chen, Yi, Zhao, Jianjie, Luo, Donglin, Tian, Wuguo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9372208/
https://www.ncbi.nlm.nih.gov/pubmed/35966288
http://dx.doi.org/10.21037/tcr-21-2686
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author Wang, Lingli
Chen, Yi
Zhao, Jianjie
Luo, Donglin
Tian, Wuguo
author_facet Wang, Lingli
Chen, Yi
Zhao, Jianjie
Luo, Donglin
Tian, Wuguo
author_sort Wang, Lingli
collection PubMed
description BACKGROUND: The prognosis of patients with breast cancer (BRCA) is difficult to predict because of the high degree of heterogeneity and complex etiological factors. Ferroptosis, an iron-dependent, new form of cell death, plays an important role in regulation of tumor growth and progression. The aim of this study was to clarify the predictive value of ferroptosis-related genes in the overall survival of patients with BRCA. METHODS: The messenger RNA expression profile and clinical information of patients with BRCA were collected from The Cancer Genome Atlas (TCGA) database. The differences between BRCA and adjacent normal tissues were analyzed, and candidates with differentially expressed ferroptosis-related genes were identified. Through Cox and LASSO analyses, the prognostic genetic characteristics of ferroptosis-related genes were established. Lastly, according to the median risk score, the patients were divided into high-risk and low-risk groups, a nomogram was constructed, and the prediction accuracy was tested. RESULTS: It was determined that the four ferroptosis related genes had a significant difference in survival in BRCA (P<0.05); a prognostic model was constructed based on the four ferroptosis related genes, and the overall survival of patients in the high-risk group was significantly worse (P<0.05). The four-gene nomogram can quantify the contribution of each index to survival, and the calibration chart shows high prediction accuracy. CONCLUSIONS: This study constructed four ferroptosis related gene characteristics and nomogram, which can effectively predict the prognosis of BRCA patients and provide new insights for future anti-cancer treatments based on ferroptosis targets.
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spelling pubmed-93722082022-08-13 Analysis and prediction model of ferroptosis related genes in breast cancer Wang, Lingli Chen, Yi Zhao, Jianjie Luo, Donglin Tian, Wuguo Transl Cancer Res Original Article BACKGROUND: The prognosis of patients with breast cancer (BRCA) is difficult to predict because of the high degree of heterogeneity and complex etiological factors. Ferroptosis, an iron-dependent, new form of cell death, plays an important role in regulation of tumor growth and progression. The aim of this study was to clarify the predictive value of ferroptosis-related genes in the overall survival of patients with BRCA. METHODS: The messenger RNA expression profile and clinical information of patients with BRCA were collected from The Cancer Genome Atlas (TCGA) database. The differences between BRCA and adjacent normal tissues were analyzed, and candidates with differentially expressed ferroptosis-related genes were identified. Through Cox and LASSO analyses, the prognostic genetic characteristics of ferroptosis-related genes were established. Lastly, according to the median risk score, the patients were divided into high-risk and low-risk groups, a nomogram was constructed, and the prediction accuracy was tested. RESULTS: It was determined that the four ferroptosis related genes had a significant difference in survival in BRCA (P<0.05); a prognostic model was constructed based on the four ferroptosis related genes, and the overall survival of patients in the high-risk group was significantly worse (P<0.05). The four-gene nomogram can quantify the contribution of each index to survival, and the calibration chart shows high prediction accuracy. CONCLUSIONS: This study constructed four ferroptosis related gene characteristics and nomogram, which can effectively predict the prognosis of BRCA patients and provide new insights for future anti-cancer treatments based on ferroptosis targets. AME Publishing Company 2022-07 /pmc/articles/PMC9372208/ /pubmed/35966288 http://dx.doi.org/10.21037/tcr-21-2686 Text en 2022 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Wang, Lingli
Chen, Yi
Zhao, Jianjie
Luo, Donglin
Tian, Wuguo
Analysis and prediction model of ferroptosis related genes in breast cancer
title Analysis and prediction model of ferroptosis related genes in breast cancer
title_full Analysis and prediction model of ferroptosis related genes in breast cancer
title_fullStr Analysis and prediction model of ferroptosis related genes in breast cancer
title_full_unstemmed Analysis and prediction model of ferroptosis related genes in breast cancer
title_short Analysis and prediction model of ferroptosis related genes in breast cancer
title_sort analysis and prediction model of ferroptosis related genes in breast cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9372208/
https://www.ncbi.nlm.nih.gov/pubmed/35966288
http://dx.doi.org/10.21037/tcr-21-2686
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