Cargando…

A prognostic model for cervical cancer based on ferroptosis-related genes

BACKGROUND: Ferroptosis is widely involved in the occurrence and development of various cancers, but a specific mechanism involving ferroptosis in cervical cancer is still unclear. METHODS: Based on the expressions of ferroptosis-related genes, a prognostic model was constructed using lasso regressi...

Descripción completa

Detalles Bibliográficos
Autores principales: Du, Huijun, Tang, Yumei, Ren, Xiaoying, Zhang, Fan, Yang, Wei, Cheng, Le, Gao, Yunan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9614331/
https://www.ncbi.nlm.nih.gov/pubmed/36313765
http://dx.doi.org/10.3389/fendo.2022.991178
_version_ 1784820177149362176
author Du, Huijun
Tang, Yumei
Ren, Xiaoying
Zhang, Fan
Yang, Wei
Cheng, Le
Gao, Yunan
author_facet Du, Huijun
Tang, Yumei
Ren, Xiaoying
Zhang, Fan
Yang, Wei
Cheng, Le
Gao, Yunan
author_sort Du, Huijun
collection PubMed
description BACKGROUND: Ferroptosis is widely involved in the occurrence and development of various cancers, but a specific mechanism involving ferroptosis in cervical cancer is still unclear. METHODS: Based on the expressions of ferroptosis-related genes, a prognostic model was constructed using lasso regression, and the overall predictive performance of this model was verified. An in-depth analysis of the prognostic model was then conducted. RESULTS: The prognostic model showed good predictive performance in both the validation and test sets. Mechanism analysis indicated that differences in the tumor microenvironment were the basis of the predictive ability of the model. Notably, CA9 mRNA was significantly overexpressed in cervical carcinoma, tissues but not in normal cervix tissues. A pair of ceRNAs (CA9/ULBP2) could be involved in the carcinogenesis and development of cervical cancer, and the potential target might be hsa-miR-34a. In addition, predicted miRNAs and drugs for these DEGs were identified. CONCLUSIONS: We constructed a prognostic model with good predictive performance, based on the expression of ferroptosis-related genes. Further research found that the ceRNA pairs of ULBP2/CA9 could regulate cervical cancer through hsa-miR-34a. These results identified the mechanism of ferroptosis in cervical cancer, and might provide novel therapeutics for cervical cancer patients.
format Online
Article
Text
id pubmed-9614331
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-96143312022-10-29 A prognostic model for cervical cancer based on ferroptosis-related genes Du, Huijun Tang, Yumei Ren, Xiaoying Zhang, Fan Yang, Wei Cheng, Le Gao, Yunan Front Endocrinol (Lausanne) Endocrinology BACKGROUND: Ferroptosis is widely involved in the occurrence and development of various cancers, but a specific mechanism involving ferroptosis in cervical cancer is still unclear. METHODS: Based on the expressions of ferroptosis-related genes, a prognostic model was constructed using lasso regression, and the overall predictive performance of this model was verified. An in-depth analysis of the prognostic model was then conducted. RESULTS: The prognostic model showed good predictive performance in both the validation and test sets. Mechanism analysis indicated that differences in the tumor microenvironment were the basis of the predictive ability of the model. Notably, CA9 mRNA was significantly overexpressed in cervical carcinoma, tissues but not in normal cervix tissues. A pair of ceRNAs (CA9/ULBP2) could be involved in the carcinogenesis and development of cervical cancer, and the potential target might be hsa-miR-34a. In addition, predicted miRNAs and drugs for these DEGs were identified. CONCLUSIONS: We constructed a prognostic model with good predictive performance, based on the expression of ferroptosis-related genes. Further research found that the ceRNA pairs of ULBP2/CA9 could regulate cervical cancer through hsa-miR-34a. These results identified the mechanism of ferroptosis in cervical cancer, and might provide novel therapeutics for cervical cancer patients. Frontiers Media S.A. 2022-10-14 /pmc/articles/PMC9614331/ /pubmed/36313765 http://dx.doi.org/10.3389/fendo.2022.991178 Text en Copyright © 2022 Du, Tang, Ren, Zhang, Yang, Cheng and Gao https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Du, Huijun
Tang, Yumei
Ren, Xiaoying
Zhang, Fan
Yang, Wei
Cheng, Le
Gao, Yunan
A prognostic model for cervical cancer based on ferroptosis-related genes
title A prognostic model for cervical cancer based on ferroptosis-related genes
title_full A prognostic model for cervical cancer based on ferroptosis-related genes
title_fullStr A prognostic model for cervical cancer based on ferroptosis-related genes
title_full_unstemmed A prognostic model for cervical cancer based on ferroptosis-related genes
title_short A prognostic model for cervical cancer based on ferroptosis-related genes
title_sort prognostic model for cervical cancer based on ferroptosis-related genes
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9614331/
https://www.ncbi.nlm.nih.gov/pubmed/36313765
http://dx.doi.org/10.3389/fendo.2022.991178
work_keys_str_mv AT duhuijun aprognosticmodelforcervicalcancerbasedonferroptosisrelatedgenes
AT tangyumei aprognosticmodelforcervicalcancerbasedonferroptosisrelatedgenes
AT renxiaoying aprognosticmodelforcervicalcancerbasedonferroptosisrelatedgenes
AT zhangfan aprognosticmodelforcervicalcancerbasedonferroptosisrelatedgenes
AT yangwei aprognosticmodelforcervicalcancerbasedonferroptosisrelatedgenes
AT chengle aprognosticmodelforcervicalcancerbasedonferroptosisrelatedgenes
AT gaoyunan aprognosticmodelforcervicalcancerbasedonferroptosisrelatedgenes
AT duhuijun prognosticmodelforcervicalcancerbasedonferroptosisrelatedgenes
AT tangyumei prognosticmodelforcervicalcancerbasedonferroptosisrelatedgenes
AT renxiaoying prognosticmodelforcervicalcancerbasedonferroptosisrelatedgenes
AT zhangfan prognosticmodelforcervicalcancerbasedonferroptosisrelatedgenes
AT yangwei prognosticmodelforcervicalcancerbasedonferroptosisrelatedgenes
AT chengle prognosticmodelforcervicalcancerbasedonferroptosisrelatedgenes
AT gaoyunan prognosticmodelforcervicalcancerbasedonferroptosisrelatedgenes