Identification of a glycolysis‐related gene signature for survival prediction of ovarian cancer patients
Abstract Background Ovarian cancer (OV) is deemed the most lethal gynecological cancer in women. The aim of this study was to construct an effective gene prognostic model for predicting overall survival (OS) in patients with OV. Methods The expression profiles of glycolysis‐related genes (GRGs) and...
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2021
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oai:doaj.org-article:f21e41a493894f62885d5ec7019731532021-11-22T09:08:48ZIdentification of a glycolysis‐related gene signature for survival prediction of ovarian cancer patients2045-763410.1002/cam4.4317https://doaj.org/article/f21e41a493894f62885d5ec7019731532021-11-01T00:00:00Zhttps://doi.org/10.1002/cam4.4317https://doaj.org/toc/2045-7634Abstract Background Ovarian cancer (OV) is deemed the most lethal gynecological cancer in women. The aim of this study was to construct an effective gene prognostic model for predicting overall survival (OS) in patients with OV. Methods The expression profiles of glycolysis‐related genes (GRGs) and clinical data of patients with OV were extracted from The Cancer Genome Atlas (TCGA) database. Univariate, multivariate, and least absolute shrinkage and selection operator Cox regression analyses were conducted, and a prognostic signature based on GRGs was constructed. The predictive ability of the signature was analyzed using training and test sets. Results A gene risk signature based on nine GRGs (ISG20, CITED2, PYGB, IRS2, ANGPTL4, TGFBI, LHX9, PC, and DDIT4) was identified to predict the survival outcome of patients with OV. The signature showed a good prognostic ability for OV, particularly high‐grade OV, in the TCGA dataset, with areas under the curve (AUC) of 0.709 and 0.762 for 3‐ and 5‐year survival, respectively. Similar results were found in the test sets, and the AUCs of 3‐, 5‐year OS were 0.714 and 0.772 in the combined test set. And our signature was an independent prognostic factor. Moreover, a nomogram combining the prediction model and clinical factors was developed. Conclusion Our study established a nine‐GRG risk model and nomogram to better predict OS in patients with OV. The risk model represents a promising and independent prognostic predictor for patients with OV. Moreover, our study on GRGs could offer guidance for the elucidation of underlying mechanisms in future studies.Dai ZhangYiche LiSi YangMeng WangJia YaoYi ZhengYujiao DengNa LiBajin WeiYing WuZhen ZhaiZhijun DaiHuafeng KangWileyarticlebioinformaticsglycolysisovarian cancerprognostic signatureNeoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282ENCancer Medicine, Vol 10, Iss 22, Pp 8222-8237 (2021) |
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bioinformatics glycolysis ovarian cancer prognostic signature Neoplasms. Tumors. Oncology. Including cancer and carcinogens RC254-282 |
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bioinformatics glycolysis ovarian cancer prognostic signature Neoplasms. Tumors. Oncology. Including cancer and carcinogens RC254-282 Dai Zhang Yiche Li Si Yang Meng Wang Jia Yao Yi Zheng Yujiao Deng Na Li Bajin Wei Ying Wu Zhen Zhai Zhijun Dai Huafeng Kang Identification of a glycolysis‐related gene signature for survival prediction of ovarian cancer patients |
description |
Abstract Background Ovarian cancer (OV) is deemed the most lethal gynecological cancer in women. The aim of this study was to construct an effective gene prognostic model for predicting overall survival (OS) in patients with OV. Methods The expression profiles of glycolysis‐related genes (GRGs) and clinical data of patients with OV were extracted from The Cancer Genome Atlas (TCGA) database. Univariate, multivariate, and least absolute shrinkage and selection operator Cox regression analyses were conducted, and a prognostic signature based on GRGs was constructed. The predictive ability of the signature was analyzed using training and test sets. Results A gene risk signature based on nine GRGs (ISG20, CITED2, PYGB, IRS2, ANGPTL4, TGFBI, LHX9, PC, and DDIT4) was identified to predict the survival outcome of patients with OV. The signature showed a good prognostic ability for OV, particularly high‐grade OV, in the TCGA dataset, with areas under the curve (AUC) of 0.709 and 0.762 for 3‐ and 5‐year survival, respectively. Similar results were found in the test sets, and the AUCs of 3‐, 5‐year OS were 0.714 and 0.772 in the combined test set. And our signature was an independent prognostic factor. Moreover, a nomogram combining the prediction model and clinical factors was developed. Conclusion Our study established a nine‐GRG risk model and nomogram to better predict OS in patients with OV. The risk model represents a promising and independent prognostic predictor for patients with OV. Moreover, our study on GRGs could offer guidance for the elucidation of underlying mechanisms in future studies. |
format |
article |
author |
Dai Zhang Yiche Li Si Yang Meng Wang Jia Yao Yi Zheng Yujiao Deng Na Li Bajin Wei Ying Wu Zhen Zhai Zhijun Dai Huafeng Kang |
author_facet |
Dai Zhang Yiche Li Si Yang Meng Wang Jia Yao Yi Zheng Yujiao Deng Na Li Bajin Wei Ying Wu Zhen Zhai Zhijun Dai Huafeng Kang |
author_sort |
Dai Zhang |
title |
Identification of a glycolysis‐related gene signature for survival prediction of ovarian cancer patients |
title_short |
Identification of a glycolysis‐related gene signature for survival prediction of ovarian cancer patients |
title_full |
Identification of a glycolysis‐related gene signature for survival prediction of ovarian cancer patients |
title_fullStr |
Identification of a glycolysis‐related gene signature for survival prediction of ovarian cancer patients |
title_full_unstemmed |
Identification of a glycolysis‐related gene signature for survival prediction of ovarian cancer patients |
title_sort |
identification of a glycolysis‐related gene signature for survival prediction of ovarian cancer patients |
publisher |
Wiley |
publishDate |
2021 |
url |
https://doaj.org/article/f21e41a493894f62885d5ec701973153 |
work_keys_str_mv |
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