Department of Otolaryngology-Head and Neck Surgery, Vanderbilt University Medical Center, Nashville, Tennessee.
Division of Epidemiology, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Cancer. 2021 Feb 15;127(4):544-553. doi: 10.1002/cncr.33309. Epub 2020 Nov 4.
The incidence of oral tongue squamous cell carcinoma (OTSCC) is increasing among younger birth cohorts. The etiology of early-onset OTSCC (diagnosed before the age of 50 years) and cancer driver genes remain largely unknown.
The Sequencing Consortium of Oral Tongue Cancer was established through the pooling of somatic mutation data of oral tongue cancer specimens (n = 227 [107 early-onset cases]) from 7 studies and The Cancer Genome Atlas. Somatic mutations at microsatellite loci and Catalog of Somatic Mutations in Cancer mutation signatures were identified. Cancer driver genes were identified with the MutSigCV and WITER algorithms. Mutation comparisons between early- and typical-onset OTSCC were evaluated via linear regression with adjustments for patient-related factors.
Two novel driver genes (ATXN1 and CDC42EP1) and 5 previously reported driver genes (TP53, CDKN2A, CASP8, NOTCH1, and FAT1) were identified. Six recurrent mutations were identified, with 4 occurring in TP53. Early-onset OTSCC had significantly fewer nonsilent mutations even after adjustments for tobacco use. No associations of microsatellite locus mutations and mutation signatures with the age of OTSCC onset were observed.
This international, multicenter consortium is the largest study to characterize the somatic mutational landscape of OTSCC and the first to suggest differences by age of onset. This study validates multiple previously identified OTSCC driver genes and proposes 2 novel cancer driver genes. In analyses by age, early-onset OTSCC had a significantly smaller somatic mutational burden that was not explained by differences in tobacco use.
This study identifies 7 specific areas in the human genetic code that could be responsible for promoting the development of tongue cancer. Tongue cancer in young patients (under the age of 50 years) has fewer overall changes to the genetic code in comparison with tongue cancer in older patients, but the authors do not think that this is due to differences in smoking rates between the 2 groups. The cause of increasing cases of tongue cancer in young patients remains unclear.
口腔舌鳞状细胞癌(OTSCC)的发病率在年轻出生队列中不断增加。早发性 OTSCC(50 岁前诊断)的病因和癌症驱动基因在很大程度上仍然未知。
通过汇集来自 7 项研究和癌症基因组图谱的口腔舌癌标本的体细胞突变数据(n = 227 [107 例早发病例]),建立了口腔舌癌测序联盟。在微卫星位点和癌症突变特征目录中鉴定体细胞突变。使用 MutSigCV 和 WITER 算法鉴定癌症驱动基因。通过线性回归评估早发性和典型性 OTSCC 之间的突变比较,并根据患者相关因素进行调整。
鉴定出两个新的驱动基因(ATXN1 和 CDC42EP1)和 5 个先前报道的驱动基因(TP53、CDKN2A、CASP8、NOTCH1 和 FAT1)。鉴定出 6 个高频突变,其中 4 个发生在 TP53 中。即使在调整吸烟因素后,早发性 OTSCC 的非同义突变也明显较少。未观察到微卫星位点突变和突变特征与 OTSCC 发病年龄之间存在关联。
该国际多中心联盟是迄今为止最大规模的 OTSCC 体细胞突变景观特征研究,也是首个提出按发病年龄差异的研究。该研究验证了多个先前鉴定的 OTSCC 驱动基因,并提出了 2 个新的癌症驱动基因。在按年龄进行的分析中,早发性 OTSCC 的体细胞突变负担明显较小,这与吸烟率的差异无关。
这是一项关于口腔舌癌的研究,口腔舌癌是一种在口腔中形成的癌症。它在年轻人中越来越常见,但确切的原因尚不清楚。这项研究确定了人类基因组中 7 个特定区域,这些区域可能导致舌癌的发展。与老年患者相比,年轻患者(50 岁以下)的遗传密码总体变化较少,但作者认为这不是由于两组患者吸烟率的差异造成的。导致年轻患者口腔舌癌病例增加的原因仍不清楚。