An immune-related seven-lncRNA signature for head and neck squamous cell carcinoma

被引:18
作者
Chen, Yue [1 ]
Luo, Tian-Qi [2 ]
Xu, Si-Si [1 ]
Chen, Chun-Yan [1 ]
Sun, Ying [1 ]
Lin, Li [1 ]
Mao, Yan-Ping [1 ]
机构
[1] Sun Yat Sen Univ, Collaborat Innovat Ctr Canc Med, Guangdong Key Lab Nasopharyngeal Carcinoma Diag &, Canc Ctr,Dept Radiat Oncol,State Key Lab Oncol So, Guangzhou, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Canc Ctr, Dept Gastr Surg, State Key Lab Oncol South China, Guangzhou, Guangdong, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
head and neck squamous cell carcinoma; immune; lncRNA; tumor microenvironment; LONG NONCODING RNA; HNSCC PATIENTS; SURVIVAL; CANCER; EXPRESSION; LANDSCAPE; PROGNOSIS; INFILTRATION; GROWTH; GENES;
D O I
10.1002/cam4.3756
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In this study, we developed a long noncoding RNA (lncRNA)-based prognostic signature for stratification of patients with head a nd neck squamous cell carcinoma (HNSCC). In total, 493 HNSCC samples obtained from the Cancer Genome Atlas database were divided into training and testing cohorts (3:2 ratio). We identified 3913 immune-related lncRNAs in the HNSCC training cohort by Pearson correlation analysis; only seven were independently associated with overall survival and were used to develop an immune-related lncRNA prognostic signature (IRLPS) grouping of HNSCC patients into high- and low-IRLPS subgroups. Univariate and multivariate Cox analyses revealed that low-IRLPS patients had a better prognosis in all the cohorts, which was retained after stratification by sex, grade, and HPV status. Although the TNM stage was also an independent prognostic factor, the IRLPS had a better discriminability with higher AUC at the 3- and 5-year follow-ups in all cohorts. Low-IRLPS samples had more immune cell infiltration and were enriched in immune-related pathways, while high- IRLPS samples were enriched in metabolic pathways. A nomogram constructed including age, TNM stage, and IRLPS showed good calibration. Thus, IRLPS improves the prognostic prediction and also distinguishes different tumor microenvironment (TME) in HNSCC patients.
引用
收藏
页码:2268 / 2285
页数:18
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