Nature. 2015 Jan 29;517(7536):576-82. doi: 10.1038/nature14129.
The Cancer Genome Atlas profiled 279 head and neck squamous cell carcinomas (HNSCCs) to provide a comprehensive landscape of somatic genomic alterations. Here we show that human-papillomavirus-associated tumours are dominated by helical domain mutations of the oncogene PIK3CA, novel alterations involving loss of TRAF3, and amplification of the cell cycle gene E2F1. Smoking-related HNSCCs demonstrate near universal loss-of-function TP53 mutations and CDKN2A inactivation with frequent copy number alterations including amplification of 3q26/28 and 11q13/22. A subgroup of oral cavity tumours with favourable clinical outcomes displayed infrequent copy number alterations in conjunction with activating mutations of HRAS or PIK3CA, coupled with inactivating mutations of CASP8, NOTCH1 and TP53. Other distinct subgroups contained loss-of-function alterations of the chromatin modifier NSD1, WNT pathway genes AJUBA and FAT1, and activation of oxidative stress factor NFE2L2, mainly in laryngeal tumours. Therapeutic candidate alterations were identified in most HNSCCs.
癌症基因组图谱项目对279例头颈部鳞状细胞癌(HNSCC)进行了分析,以全面呈现体细胞基因组改变的情况。我们在此表明,人乳头瘤病毒相关肿瘤以癌基因PIK3CA的螺旋结构域突变、涉及TRAF3缺失的新型改变以及细胞周期基因E2F1的扩增为主。与吸烟相关的HNSCC表现出近乎普遍的功能丧失型TP53突变和CDKN2A失活,伴有频繁的拷贝数改变,包括3q26/28和11q13/22的扩增。一组具有良好临床预后的口腔肿瘤亚组显示,拷贝数改变很少,同时伴有HRAS或PIK3CA的激活突变,以及CASP8、NOTCH1和TP53的失活突变。其他不同的亚组包含染色质修饰因子NSD1、WNT通路基因AJUBA和FAT1的功能丧失型改变,以及氧化应激因子NFE2L2的激活,主要见于喉肿瘤。在大多数HNSCC中都发现了潜在的治疗靶点改变。