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A nomogram based on A-to-I RNA editing predicting overall survival of patients with lung squamous carcinoma

BACKGROUND: Adenosine-to-inosine RNA editing (ATIRE) is characterized as non-mutational epigenetic reprogramming hallmark of cancer, while little is known about its predictive role in cancer survival. METHODS: To explore survival-related ATIRE events in lung squamous cell carcinoma (LUSC), ATIRE pro...

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Autores principales: Liu, Li, Liu, Jun, Deng, Xiaoliang, Tu, Li, Zhao, Zhuxiang, Xie, Chenli, Yang, Lei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9241197/
https://www.ncbi.nlm.nih.gov/pubmed/35768804
http://dx.doi.org/10.1186/s12885-022-09773-0
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author Liu, Li
Liu, Jun
Deng, Xiaoliang
Tu, Li
Zhao, Zhuxiang
Xie, Chenli
Yang, Lei
author_facet Liu, Li
Liu, Jun
Deng, Xiaoliang
Tu, Li
Zhao, Zhuxiang
Xie, Chenli
Yang, Lei
author_sort Liu, Li
collection PubMed
description BACKGROUND: Adenosine-to-inosine RNA editing (ATIRE) is characterized as non-mutational epigenetic reprogramming hallmark of cancer, while little is known about its predictive role in cancer survival. METHODS: To explore survival-related ATIRE events in lung squamous cell carcinoma (LUSC), ATIRE profile, gene expression data, and corresponding clinical information of LUSC patients were downloaded from the TCGA database. Patients were randomly divided into a training (n = 134) and validation cohort (n = 94). Cox proportional hazards regression followed by least absolute shrinkage and selection operator algorithm were performed to identify survival-related ATIRE sites and to generate ATIRE risk score. Then a nomogram was constructed to predict overall survival (OS) of LUSC patients. The correlation of ATIRE level and host gene expression and ATIREs’ effect on transcriptome expression were analyzed. RESULTS: Seven ATIRE sites that were TMEM120B chr12:122215052A > I, HMOX2 chr16:4533713A > I, CALCOCO2 chr17:46941503A > I, LONP2 chr16:48388244A > I, ZNF440 chr19:11945758A > I, CLCC1 chr1:109474650A > I, and CHMP3 chr2:86754288A > I were identified to generate the risk score, of which high levers were significantly associated with worse OS and progression-free survival in both the training and validation sets. High risk-score was also associated with advanced T stages and worse clinical stages. The nomogram performed well in predicting OS probability of LUSC. Moreover, the editing of ATIRE sites exerted a significant association with expression of host genes and affected several cancer-related pathways. CONCLUSIONS: This is the first comprehensive study to analyze the role of ATIRE events in predicting LUSC survival. The AITRE-based model might serve as a novel tool for LUSC survival prediction. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-022-09773-0.
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spelling pubmed-92411972022-06-30 A nomogram based on A-to-I RNA editing predicting overall survival of patients with lung squamous carcinoma Liu, Li Liu, Jun Deng, Xiaoliang Tu, Li Zhao, Zhuxiang Xie, Chenli Yang, Lei BMC Cancer Research BACKGROUND: Adenosine-to-inosine RNA editing (ATIRE) is characterized as non-mutational epigenetic reprogramming hallmark of cancer, while little is known about its predictive role in cancer survival. METHODS: To explore survival-related ATIRE events in lung squamous cell carcinoma (LUSC), ATIRE profile, gene expression data, and corresponding clinical information of LUSC patients were downloaded from the TCGA database. Patients were randomly divided into a training (n = 134) and validation cohort (n = 94). Cox proportional hazards regression followed by least absolute shrinkage and selection operator algorithm were performed to identify survival-related ATIRE sites and to generate ATIRE risk score. Then a nomogram was constructed to predict overall survival (OS) of LUSC patients. The correlation of ATIRE level and host gene expression and ATIREs’ effect on transcriptome expression were analyzed. RESULTS: Seven ATIRE sites that were TMEM120B chr12:122215052A > I, HMOX2 chr16:4533713A > I, CALCOCO2 chr17:46941503A > I, LONP2 chr16:48388244A > I, ZNF440 chr19:11945758A > I, CLCC1 chr1:109474650A > I, and CHMP3 chr2:86754288A > I were identified to generate the risk score, of which high levers were significantly associated with worse OS and progression-free survival in both the training and validation sets. High risk-score was also associated with advanced T stages and worse clinical stages. The nomogram performed well in predicting OS probability of LUSC. Moreover, the editing of ATIRE sites exerted a significant association with expression of host genes and affected several cancer-related pathways. CONCLUSIONS: This is the first comprehensive study to analyze the role of ATIRE events in predicting LUSC survival. The AITRE-based model might serve as a novel tool for LUSC survival prediction. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-022-09773-0. BioMed Central 2022-06-29 /pmc/articles/PMC9241197/ /pubmed/35768804 http://dx.doi.org/10.1186/s12885-022-09773-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Liu, Li
Liu, Jun
Deng, Xiaoliang
Tu, Li
Zhao, Zhuxiang
Xie, Chenli
Yang, Lei
A nomogram based on A-to-I RNA editing predicting overall survival of patients with lung squamous carcinoma
title A nomogram based on A-to-I RNA editing predicting overall survival of patients with lung squamous carcinoma
title_full A nomogram based on A-to-I RNA editing predicting overall survival of patients with lung squamous carcinoma
title_fullStr A nomogram based on A-to-I RNA editing predicting overall survival of patients with lung squamous carcinoma
title_full_unstemmed A nomogram based on A-to-I RNA editing predicting overall survival of patients with lung squamous carcinoma
title_short A nomogram based on A-to-I RNA editing predicting overall survival of patients with lung squamous carcinoma
title_sort nomogram based on a-to-i rna editing predicting overall survival of patients with lung squamous carcinoma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9241197/
https://www.ncbi.nlm.nih.gov/pubmed/35768804
http://dx.doi.org/10.1186/s12885-022-09773-0
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