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

Lessons learned from next-generation sequencing in head and neck cancer.
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DOI:
10.1002/hed.23100
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发表时间:
2013-03
影响因子:
2.9
通讯作者:
Agrawal, Nishant
Agrawal, Nishant
中科院分区:
医学2区
文献类型:
--
作者:
Loyo, Myriam;Li, Ryan J.;Bettegowda, Chetan;Pickering, Curtis R.;Frederick, Mitchell J.;Myers, Jeffrey N.;Agrawal, Nishant

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科学创新使整个外显子组捕获和癌症基因组的大规模平行测序成为可能。在头颈癌中,下一代测序使我们进一步了解鳞状细胞癌的突变谱。由于这些新技术,在NOTCH1中发现了频繁发生的突变,这是一种以前与头颈癌无关的基因。目前的综述描述了头颈癌中最常见的突变:TP53,NOTCH1,HRAS,PIK3CA和CDKN2A。重点放在所涉及的细胞通路,临床相关性,和潜在的治疗干预。此外,人乳头瘤病毒的突变模式的影响进行了讨论。
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.
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