Construction of Prognostic Prediction Model for Lung Squamous Cell Carcinoma Based on Cuproptosis-related LncRNAs

Objective To develop a new risk scoring model based on cuproptosis-related lncRNAs (CRLs) to predict the prognosis of lung squamous cell carcinoma (LUSC). Methods Data were obtained mainly from TCGA and GTEx databases. Univariate Cox, Lasso, and multivariate Cox regression analyses were conducted to...

Full description

Bibliographic Details
Main Authors: AN Mengxia, WANG Pingyu
Format: Article
Language:zho
Published: Magazine House of Cancer Research on Prevention and Treatment 2023-11-01
Series:Zhongliu Fangzhi Yanjiu
Subjects:
Online Access:http://www.zlfzyj.com/EN/10.3971/j.issn.1000-8578.2023.23.0370
_version_ 1797401544593768448
author AN Mengxia
WANG Pingyu
author_facet AN Mengxia
WANG Pingyu
author_sort AN Mengxia
collection DOAJ
description Objective To develop a new risk scoring model based on cuproptosis-related lncRNAs (CRLs) to predict the prognosis of lung squamous cell carcinoma (LUSC). Methods Data were obtained mainly from TCGA and GTEx databases. Univariate Cox, Lasso, and multivariate Cox regression analyses were conducted to determine CRLs that affect the prognosis of LUSC and establish a risk scoring model. The ability of risk score characteristics to independently predict LUSC survival was compared with that of clinical characteristics by calculating the area under the ROC curve (AUC). Immune-related functions and immune checkpoint differences were compared between high- and low-risk groups. Results Nine CRLs were selected as independent prognostic lncRNAs for LUSC, and a risk scoring model was developed. Risk score was the influence factor for the prognosis of LUSC. The AUC values predicted by the risk score model for 1-, 3-, and 5-year survival rates of patients with LUSC were 0.710, 0.718, and 0.743, respectively. The high- and low-risk groups were partly statistically different in terms of immune-related functional assays and immune checkpoint assays (P < 0.05). Conclusion The risk scoring model developed based on nine CRLs could predict the prognosis and immune therapy response of patients with LUSC in clinical practice.
first_indexed 2024-03-09T02:12:36Z
format Article
id doaj.art-54ee816cea26446cac40e4d862784702
institution Directory Open Access Journal
issn 1000-8578
language zho
last_indexed 2024-03-09T02:12:36Z
publishDate 2023-11-01
publisher Magazine House of Cancer Research on Prevention and Treatment
record_format Article
series Zhongliu Fangzhi Yanjiu
spelling doaj.art-54ee816cea26446cac40e4d8627847022023-12-07T07:46:12ZzhoMagazine House of Cancer Research on Prevention and TreatmentZhongliu Fangzhi Yanjiu1000-85782023-11-0150111084109010.3971/j.issn.1000-8578.2023.23.03708578.2023.23.0370Construction of Prognostic Prediction Model for Lung Squamous Cell Carcinoma Based on Cuproptosis-related LncRNAsAN Mengxia0WANG Pingyu1School of Public Health and Management, Binzhou Medical College, Yantai 264003, ChinaSchool of Public Health and Management, Binzhou Medical College, Yantai 264003, ChinaObjective To develop a new risk scoring model based on cuproptosis-related lncRNAs (CRLs) to predict the prognosis of lung squamous cell carcinoma (LUSC). Methods Data were obtained mainly from TCGA and GTEx databases. Univariate Cox, Lasso, and multivariate Cox regression analyses were conducted to determine CRLs that affect the prognosis of LUSC and establish a risk scoring model. The ability of risk score characteristics to independently predict LUSC survival was compared with that of clinical characteristics by calculating the area under the ROC curve (AUC). Immune-related functions and immune checkpoint differences were compared between high- and low-risk groups. Results Nine CRLs were selected as independent prognostic lncRNAs for LUSC, and a risk scoring model was developed. Risk score was the influence factor for the prognosis of LUSC. The AUC values predicted by the risk score model for 1-, 3-, and 5-year survival rates of patients with LUSC were 0.710, 0.718, and 0.743, respectively. The high- and low-risk groups were partly statistically different in terms of immune-related functional assays and immune checkpoint assays (P < 0.05). Conclusion The risk scoring model developed based on nine CRLs could predict the prognosis and immune therapy response of patients with LUSC in clinical practice.http://www.zlfzyj.com/EN/10.3971/j.issn.1000-8578.2023.23.0370lung squamous cell carcinomacuproptosislncrnaimmune therapy
spellingShingle AN Mengxia
WANG Pingyu
Construction of Prognostic Prediction Model for Lung Squamous Cell Carcinoma Based on Cuproptosis-related LncRNAs
Zhongliu Fangzhi Yanjiu
lung squamous cell carcinoma
cuproptosis
lncrna
immune therapy
title Construction of Prognostic Prediction Model for Lung Squamous Cell Carcinoma Based on Cuproptosis-related LncRNAs
title_full Construction of Prognostic Prediction Model for Lung Squamous Cell Carcinoma Based on Cuproptosis-related LncRNAs
title_fullStr Construction of Prognostic Prediction Model for Lung Squamous Cell Carcinoma Based on Cuproptosis-related LncRNAs
title_full_unstemmed Construction of Prognostic Prediction Model for Lung Squamous Cell Carcinoma Based on Cuproptosis-related LncRNAs
title_short Construction of Prognostic Prediction Model for Lung Squamous Cell Carcinoma Based on Cuproptosis-related LncRNAs
title_sort construction of prognostic prediction model for lung squamous cell carcinoma based on cuproptosis related lncrnas
topic lung squamous cell carcinoma
cuproptosis
lncrna
immune therapy
url http://www.zlfzyj.com/EN/10.3971/j.issn.1000-8578.2023.23.0370
work_keys_str_mv AT anmengxia constructionofprognosticpredictionmodelforlungsquamouscellcarcinomabasedoncuproptosisrelatedlncrnas
AT wangpingyu constructionofprognosticpredictionmodelforlungsquamouscellcarcinomabasedoncuproptosisrelatedlncrnas