Stemness-related lncRNAs signature as a biologic prognostic model for head and neck squamous cell carcinoma

被引:0
|
作者
Zejun Xu
Min Zhang
Zhiqiang Guo
Lin Chen
Xiaolei Yang
Xiaoyu Li
Qian Liang
Yuqing Tang
Jian Liu
机构
[1] Hainan University,School of Life Sciences
[2] Institute of Biological Anthropology of Jinzhou Medical University,Department of Otolaryngology
[3] Xiangya Hospital,Head and Neck Surgery
[4] Central South University,Department of Pathology
[5] QingPu Branch of Zhongshan Hospital Affiliated to Fudan University,School of Biological Sciences
[6] Community Health Service Center of Zhongshan Street,undefined
[7] Fourth People’s Hospital of Jinan,undefined
[8] University of Texas Southwestern Medical Center,undefined
[9] University of Bristol,undefined
来源
Apoptosis | 2023年 / 28卷
关键词
Head and neck squamous cell carcinoma; LncRNAs; Cancer stem cells; Prognostic model; Immune microenvironment;
D O I
暂无
中图分类号
学科分类号
摘要
Cancer stem cells (CSCs) and long non-coding RNAs (lncRNAs) are particularly important for tumor cell growth and migration, and recurrence and drug resistance, including head and neck squamous cell carcinoma (HNSCC). The purpose of this study was to explore stemness-related lncRNAs (SRlncRNAs) that could be used for prognosis of patients with HNSCC. HNSCC RNA sequencing data and matched clinical data were obtained from TCGA database, and stem cell characteristic genes related to HNSCC mRNAsi were obtained from the online database by WGCNA analysis, respectively. Further, SRlncRNAs were obtained. Then, the prognostic model was constructed to forecast patient survival through univariate Cox regression and LASSO-Cox method based on SRlncRNAs. Kaplan–Meier, ROC and AUC were used to evaluate the predictive ability of the model. Moreover, we probed the underlying biological functions, signalling pathways and immune status hidden within differences in prognosis of patients. We explored whether the model could guide personalized treatments included immunotherapy and chemotherapy for HNSCC patients. At last, RT‐qPCR was performed to analyze the expressions levels of SRlncRNAs in HNSCC cell lines. A SRlncRNAs signature was identified based on 5 SRlncRNAs (AC004943.2, AL022328.1, MIR9-3HG, AC015878.1 and FOXD2-AS1) in HNSCC. Also, risk scores were correlated with the abundance of tumor-infiltrating immune cells, whereas HNSCC-nominated chemotherapy drugs were considerably different from one another. The final finding was that these SRlncRNAs were abnormally expressed in HNSCCCS according to the results of RT-qPCR. These 5 SRlncRNAs signature, as a potential prognostic biomarker, can be utilized for personalized medicine in HNSCC patients.
引用
收藏
页码:860 / 880
页数:20
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