Lessons learned from next-generation sequencing in head and neck cancer

被引:48
|
作者
Loyo, Myriam [1 ]
Li, Ryan J. [1 ]
Bettegowda, Chetan [2 ]
Pickering, Curtis R. [3 ]
Frederick, Mitchell J. [3 ]
Myers, Jeffrey N. [3 ]
Agrawal, Nishant [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Otolaryngol Head & Neck Surg, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Neurosurg, Baltimore, MD 21205 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Head & Neck Surg, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
next generation sequencing; mutations; oncogene; tumor suppressor gene; head and neck squamous cell carcinoma; SQUAMOUS-CELL-CARCINOMA; GROWTH-FACTOR RECEPTOR; PHASE-II TRIAL; HUMAN-PAPILLOMAVIRUS; TUMOR-SUPPRESSOR; P53; GENE; OROPHARYNGEAL CANCER; H-RAS; SIGNALING PATHWAYS; THERAPEUTIC TARGET;
D O I
10.1002/hed.23100
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Scientific innovation has enabled whole exome capture and massively parallel sequencing of cancer genomes. In head and neck cancer, next-generation sequencing has granted us further understanding of the mutational spectrum of squamous cell carcinoma. As a result of these new technologies, frequently occurring mutations were identified in NOTCH1, a gene that had not previously been implicated in head and neck cancer. The current review describes the most common mutations in head and neck cancer: TP53, NOTCH1, HRAS, PIK3CA, and CDKN2A. Emphasis is placed on the involved cellular pathways, clinical correlations, and potential therapeutic interventions. Additionally, the implications of human papillomavirus on mutation patterns are discussed. (C) 2012 Wiley Periodicals, Inc. Head Neck 35: 454-463, 2013
引用
收藏
页码:454 / 463
页数:10
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