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Ferroptosis-related Genes for Overall Survival Prediction in Patients with Colorectal Cancer can be Inhibited by Gallic acid

Colorectal cancer (CRC) is one of the most deadly malignant tumors, which seriously threatens human health. Ferroptosis, a new type of iron-dependent cell regulatory necrosis. Inducing ferroptosis of tumor cells is regarded as a potential treatment strategy. However, the prognostic value of ferropto...

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Autores principales: Hong, Zongchao, Tang, Peili, Liu, Bo, Ran, Chongwang, Yuan, Chong, Zhang, Ying, Lu, Yi, Duan, Xueyun, Yang, Yanfang, Wu, Hezhen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8040315/
https://www.ncbi.nlm.nih.gov/pubmed/33867820
http://dx.doi.org/10.7150/ijbs.57164
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author Hong, Zongchao
Tang, Peili
Liu, Bo
Ran, Chongwang
Yuan, Chong
Zhang, Ying
Lu, Yi
Duan, Xueyun
Yang, Yanfang
Wu, Hezhen
author_facet Hong, Zongchao
Tang, Peili
Liu, Bo
Ran, Chongwang
Yuan, Chong
Zhang, Ying
Lu, Yi
Duan, Xueyun
Yang, Yanfang
Wu, Hezhen
author_sort Hong, Zongchao
collection PubMed
description Colorectal cancer (CRC) is one of the most deadly malignant tumors, which seriously threatens human health. Ferroptosis, a new type of iron-dependent cell regulatory necrosis. Inducing ferroptosis of tumor cells is regarded as a potential treatment strategy. However, the prognostic value of ferroptosis-related genes in CRC remains to be further elucidated. Gallic acid, widely used in the chemical, pharmaceutical, and food fields, is a dietary supplement with potential prescription significance. In this study, the mRNA expression profiles and corresponding clinical data of CRC patients were downloaded from public databases. Gene Expression Profiling Interactive Analysis (GEPIA) was used to evaluate the expression levels of ferroptosis-related genes. In addition, bioinformatics analysis showed the prognostic value of ferroptosis-related genes in CRC. Molecular docking predicts the binding status of gallic acid and ferroptosis-related genes. The experiment confirmed the correctness of the predicted results. Our results show that in the TCGA cohort, 30 ferroptosis-related genes are differentially expressed between CRC and adjacent normal tissues. Among them, eight differentially expressed genes are related to overall survival. Gallic acid can bind to ferroptosis-related targets and regulate the expression of corresponding proteins, and ferroptosis inhibitors reversed the experimental results. In summary, eight new ferroptosis-related genes can be used to predict the prognosis of CRC. Gallic acid can improve CRC by regulating ferroptosis.
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spelling pubmed-80403152021-04-16 Ferroptosis-related Genes for Overall Survival Prediction in Patients with Colorectal Cancer can be Inhibited by Gallic acid Hong, Zongchao Tang, Peili Liu, Bo Ran, Chongwang Yuan, Chong Zhang, Ying Lu, Yi Duan, Xueyun Yang, Yanfang Wu, Hezhen Int J Biol Sci Research Paper Colorectal cancer (CRC) is one of the most deadly malignant tumors, which seriously threatens human health. Ferroptosis, a new type of iron-dependent cell regulatory necrosis. Inducing ferroptosis of tumor cells is regarded as a potential treatment strategy. However, the prognostic value of ferroptosis-related genes in CRC remains to be further elucidated. Gallic acid, widely used in the chemical, pharmaceutical, and food fields, is a dietary supplement with potential prescription significance. In this study, the mRNA expression profiles and corresponding clinical data of CRC patients were downloaded from public databases. Gene Expression Profiling Interactive Analysis (GEPIA) was used to evaluate the expression levels of ferroptosis-related genes. In addition, bioinformatics analysis showed the prognostic value of ferroptosis-related genes in CRC. Molecular docking predicts the binding status of gallic acid and ferroptosis-related genes. The experiment confirmed the correctness of the predicted results. Our results show that in the TCGA cohort, 30 ferroptosis-related genes are differentially expressed between CRC and adjacent normal tissues. Among them, eight differentially expressed genes are related to overall survival. Gallic acid can bind to ferroptosis-related targets and regulate the expression of corresponding proteins, and ferroptosis inhibitors reversed the experimental results. In summary, eight new ferroptosis-related genes can be used to predict the prognosis of CRC. Gallic acid can improve CRC by regulating ferroptosis. Ivyspring International Publisher 2021-03-01 /pmc/articles/PMC8040315/ /pubmed/33867820 http://dx.doi.org/10.7150/ijbs.57164 Text en © The author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Hong, Zongchao
Tang, Peili
Liu, Bo
Ran, Chongwang
Yuan, Chong
Zhang, Ying
Lu, Yi
Duan, Xueyun
Yang, Yanfang
Wu, Hezhen
Ferroptosis-related Genes for Overall Survival Prediction in Patients with Colorectal Cancer can be Inhibited by Gallic acid
title Ferroptosis-related Genes for Overall Survival Prediction in Patients with Colorectal Cancer can be Inhibited by Gallic acid
title_full Ferroptosis-related Genes for Overall Survival Prediction in Patients with Colorectal Cancer can be Inhibited by Gallic acid
title_fullStr Ferroptosis-related Genes for Overall Survival Prediction in Patients with Colorectal Cancer can be Inhibited by Gallic acid
title_full_unstemmed Ferroptosis-related Genes for Overall Survival Prediction in Patients with Colorectal Cancer can be Inhibited by Gallic acid
title_short Ferroptosis-related Genes for Overall Survival Prediction in Patients with Colorectal Cancer can be Inhibited by Gallic acid
title_sort ferroptosis-related genes for overall survival prediction in patients with colorectal cancer can be inhibited by gallic acid
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8040315/
https://www.ncbi.nlm.nih.gov/pubmed/33867820
http://dx.doi.org/10.7150/ijbs.57164
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