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Identification of a Nomogram with an Autophagy-Related Risk Signature for Survival Prediction in Patients with Glioma
BACKGROUND: Glioma is a common type of tumor in the central nervous system characterized by high morbidity and mortality. Autophagy plays vital roles in the development and progression of glioma, and is involved in both normal physiological and various pathophysiological progresses. PATIENTS AND MET...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857975/ https://www.ncbi.nlm.nih.gov/pubmed/35210825 http://dx.doi.org/10.2147/IJGM.S335571 |
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author | Fu, Xiaofeng Hong, Luwei Gong, Haiying Kan, Guangjuan Zhang, Pengfei Cui, Ting-Ting Fan, Gonglin Si, Xing Zhu, Jiang |
author_facet | Fu, Xiaofeng Hong, Luwei Gong, Haiying Kan, Guangjuan Zhang, Pengfei Cui, Ting-Ting Fan, Gonglin Si, Xing Zhu, Jiang |
author_sort | Fu, Xiaofeng |
collection | PubMed |
description | BACKGROUND: Glioma is a common type of tumor in the central nervous system characterized by high morbidity and mortality. Autophagy plays vital roles in the development and progression of glioma, and is involved in both normal physiological and various pathophysiological progresses. PATIENTS AND METHODS: A total of 531 autophagy-related genes (ARGs) were obtained and 1738 glioma patients were collected from three public databases. We performed least absolute shrinkage and selection operator regression to identify the optimal prognosis-related genes and constructed an autophagy-related risk signature. The performance of the signature was validated by receiver operating characteristic analysis, survival analysis, clinic correlation analysis, and Cox regression. A nomogram model was established by using multivariate Cox regression analysis. Schoenfeld’s global and individual test were used to estimate time-varying covariance for the assumption of the Cox proportional hazard regression analysis. The R programming language was used as the main data analysis and visualizing tool. RESULTS: An overall survival-related risk signature consisting of 15 ARGs was constructed and significantly stratified glioma patients into high- and low-risk groups (P < 0.0001). The area under the ROC curve of 1-, 3-, 5-year survival was 0.890, 0.923, and 0.889, respectively. Univariate and multivariate Cox analyses indicated that the risk signature was a satisfactory independent prognostic factor. Moreover, a nomogram model integrating risk signature with clinical information for predicting survival rates of patients with glioma was constructed (C-index=0.861±0.024). CONCLUSION: This study constructed a novel and reliable ARG-related risk signature, which was verified as a satisfactory prognostic marker. The nomogram model could provide a reference for individually predicting the prognosis for each patient with glioma and promoting the selection of optimal treatment. |
format | Online Article Text |
id | pubmed-8857975 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-88579752022-02-23 Identification of a Nomogram with an Autophagy-Related Risk Signature for Survival Prediction in Patients with Glioma Fu, Xiaofeng Hong, Luwei Gong, Haiying Kan, Guangjuan Zhang, Pengfei Cui, Ting-Ting Fan, Gonglin Si, Xing Zhu, Jiang Int J Gen Med Original Research BACKGROUND: Glioma is a common type of tumor in the central nervous system characterized by high morbidity and mortality. Autophagy plays vital roles in the development and progression of glioma, and is involved in both normal physiological and various pathophysiological progresses. PATIENTS AND METHODS: A total of 531 autophagy-related genes (ARGs) were obtained and 1738 glioma patients were collected from three public databases. We performed least absolute shrinkage and selection operator regression to identify the optimal prognosis-related genes and constructed an autophagy-related risk signature. The performance of the signature was validated by receiver operating characteristic analysis, survival analysis, clinic correlation analysis, and Cox regression. A nomogram model was established by using multivariate Cox regression analysis. Schoenfeld’s global and individual test were used to estimate time-varying covariance for the assumption of the Cox proportional hazard regression analysis. The R programming language was used as the main data analysis and visualizing tool. RESULTS: An overall survival-related risk signature consisting of 15 ARGs was constructed and significantly stratified glioma patients into high- and low-risk groups (P < 0.0001). The area under the ROC curve of 1-, 3-, 5-year survival was 0.890, 0.923, and 0.889, respectively. Univariate and multivariate Cox analyses indicated that the risk signature was a satisfactory independent prognostic factor. Moreover, a nomogram model integrating risk signature with clinical information for predicting survival rates of patients with glioma was constructed (C-index=0.861±0.024). CONCLUSION: This study constructed a novel and reliable ARG-related risk signature, which was verified as a satisfactory prognostic marker. The nomogram model could provide a reference for individually predicting the prognosis for each patient with glioma and promoting the selection of optimal treatment. Dove 2022-02-15 /pmc/articles/PMC8857975/ /pubmed/35210825 http://dx.doi.org/10.2147/IJGM.S335571 Text en © 2022 Fu et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Fu, Xiaofeng Hong, Luwei Gong, Haiying Kan, Guangjuan Zhang, Pengfei Cui, Ting-Ting Fan, Gonglin Si, Xing Zhu, Jiang Identification of a Nomogram with an Autophagy-Related Risk Signature for Survival Prediction in Patients with Glioma |
title | Identification of a Nomogram with an Autophagy-Related Risk Signature for Survival Prediction in Patients with Glioma |
title_full | Identification of a Nomogram with an Autophagy-Related Risk Signature for Survival Prediction in Patients with Glioma |
title_fullStr | Identification of a Nomogram with an Autophagy-Related Risk Signature for Survival Prediction in Patients with Glioma |
title_full_unstemmed | Identification of a Nomogram with an Autophagy-Related Risk Signature for Survival Prediction in Patients with Glioma |
title_short | Identification of a Nomogram with an Autophagy-Related Risk Signature for Survival Prediction in Patients with Glioma |
title_sort | identification of a nomogram with an autophagy-related risk signature for survival prediction in patients with glioma |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857975/ https://www.ncbi.nlm.nih.gov/pubmed/35210825 http://dx.doi.org/10.2147/IJGM.S335571 |
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