The Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Science. 2011 Aug 26;333(6046):1157-60. doi: 10.1126/science.1208130. Epub 2011 Jul 28.
Head and neck squamous cell carcinoma (HNSCC) is a common, morbid, and frequently lethal malignancy. To uncover its mutational spectrum, we analyzed whole-exome sequencing data from 74 tumor-normal pairs. The majority exhibited a mutational profile consistent with tobacco exposure; human papillomavirus was detectable by sequencing DNA from infected tumors. In addition to identifying previously known HNSCC genes (TP53, CDKN2A, PTEN, PIK3CA, and HRAS), our analysis revealed many genes not previously implicated in this malignancy. At least 30% of cases harbored mutations in genes that regulate squamous differentiation (for example, NOTCH1, IRF6, and TP63), implicating its dysregulation as a major driver of HNSCC carcinogenesis. More generally, the results indicate the ability of large-scale sequencing to reveal fundamental tumorigenic mechanisms.
头颈部鳞状细胞癌(HNSCC)是一种常见的、严重的、且常常致命的恶性肿瘤。为了揭示其突变谱,我们分析了 74 对肿瘤-正常组织的全外显子组测序数据。大多数肿瘤表现出与烟草暴露一致的突变特征;通过对感染肿瘤的 DNA 进行测序,可以检测到人乳头瘤病毒。除了鉴定先前已知的 HNSCC 基因(TP53、CDKN2A、PTEN、PIK3CA 和 HRAS)外,我们的分析还揭示了许多以前与这种恶性肿瘤无关的基因。至少 30%的病例携带调节鳞状细胞分化的基因(例如 NOTCH1、IRF6 和 TP63)的突变,提示其失调是 HNSCC 致癌发生的主要驱动因素。更普遍地说,这些结果表明大规模测序能够揭示基本的肿瘤发生机制。