Prognostic microRNA signatures derived from The Cancer Genome Atlas for head and neck squamous cell carcinomas

被引:70
|
作者
Wong, Nathan [1 ,2 ]
Khwaja, Shariq S. [1 ]
Baker, Callie M. [1 ]
Gay, Hiram A. [1 ]
Thorstad, Wade L. [1 ]
Daly, Mackenzie D. [1 ]
Lewis, James S., Jr. [3 ,4 ]
Wang, Xiaowei [1 ,2 ]
机构
[1] Washington Univ, Sch Med, Dept Radiat Oncol, 4511 Forest Pk Ave, St Louis, MO 63108 USA
[2] Washington Univ, Dept Biomed Engn, St Louis, MO USA
[3] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO USA
[4] Vanderbilt Univ, Med Ctr, Dept Pathol Microbiol & Immunol, Nashville, TN USA
来源
CANCER MEDICINE | 2016年 / 5卷 / 07期
基金
美国国家卫生研究院;
关键词
Gene signature; head and neck cancer; microRNA; oropharyngeal cancer; prognosis; The Cancer Genome Atlas; HUMAN-PAPILLOMAVIRUS; OROPHARYNGEAL CANCER; DE-ESCALATION; HPV; PLATFORM; PANEL;
D O I
10.1002/cam4.718
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Identification of novel prognostic biomarkers typically requires a large dataset which provides sufficient statistical power for discovery research. To this end, we took advantage of the high-throughput data from The Cancer Genome Atlas (TCGA) to identify a set of prognostic biomarkers in head and neck squamous cell carcinomas (HNSCC) including oropharyngeal squamous cell carcinoma (OPSCC) and other subtypes. In this study, we analyzed miRNA-seq data obtained from TCGA patients to identify prognostic biomarkers for OPSCC. The identified miRNAs were further tested with an independent cohort. miRNA-seq data from TCGA was also analyzed to identify prognostic miRNAs in oral cavity squamous cell carcinoma (OSCC) and laryngeal squamous cell carcinoma (LSCC). Our study identified that miR-193b-3p and miR-455-5p were positively associated with survival, and miR-92a-3p and miR-497-5p were negatively associated with survival in OPSCC. A combined expression signature of these four miRNAs was prognostic of overall survival in OPSCC, and more importantly, this signature was validated in an independent OPSCC cohort. Furthermore, we identified four miRNAs each in OSCC and LSCC that were prognostic of survival, and combined signatures were specific for subtypes of HNSCC. A robust 4-miRNA prognostic signature in OPSCC, as well as prognostic signatures in other subtypes of HNSCC, was developed using sequencing data from TCGA as the primary source. This demonstrates the power of using TCGA as a potential resource to develop prognostic tools for improving individualized patient care.
引用
收藏
页码:1619 / 1628
页数:10
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