Wang Qiyan, Bai Jian, Abliz Amir, Liu Ying, Gong Kenan, Li Jingjing, Shi Wenjie, Pan Yaqi, Liu Fangfang, Lai Shujuan, Yang Haijun, Lu Changdong, Zhang Lixin, Chen Wei, Xu Ruiping, Cai Hong, Ke Yang, Zeng Changqing
MOE Key Laboratory of Carcinogenesis and Translational Research, Laboratory of Genetics, Peking University, Cancer Hospital & Institute, Beijing 100142, China; Beijing University of Chinese Medicine, Beijing 100029, China.
CAS Key Laboratory of Genomic and Precision Medicine, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, China.
Genomics Proteomics Bioinformatics. 2015 Aug;13(4):258-70. doi: 10.1016/j.gpb.2015.06.003. Epub 2015 Sep 16.
Esophageal squamous cell carcinoma (ESCC) has a high mortality rate. To determine the molecular basis of ESCC development, this study sought to identify characteristic genome-wide alterations in ESCC, including exonic mutations and structural alterations. The clinical implications of these genetic alterations were also analyzed. Exome sequencing and verification were performed for nine pairs of ESCC and the matched blood samples, followed by validation with additional samples using Sanger sequencing. Whole-genome SNP arrays were employed to detect copy number alteration (CNA) and loss of heterozygosity (LOH) in 55 cases, including the nine ESCC samples subjected to exome sequencing. A total of 108 non-synonymous somatic mutations (NSSMs) in 102 genes were verified in nine patients. The chromatin modification process was found to be enriched in our gene ontology (GO) analysis. Tumor genomes with TP53 mutations were significantly more unstable than those without TP53 mutations. In terms of the landscape of genomic alterations, deletion of 9p21.3 covering CDKN2A/2B (30.9%), amplification of 11q13.3 covering CCND1 (30.9%), and TP53 point mutation (50.9%) occurred in two-thirds of the cases. These results suggest that the deregulation of the G1 phase during the cell cycle is a key event in ESCC. Furthermore, six minimal common regions were found to be significantly altered in ESCC samples and three of them, 9p21.3, 7p11.2, and 3p12.1, were associated with lymph node metastasis. With the high correlation of TP53 mutation and genomic instability in ESCC, the amplification of CCND1, the deletion of CDKN2A/2B, and the somatic mutation of TP53 appear to play pivotal roles via G1 deregulation and therefore helps to classify this cancer into different genomic subtypes. These findings provide clinical significance that could be useful in future molecular diagnoses and therapeutic targeting.
食管鳞状细胞癌(ESCC)死亡率很高。为了确定ESCC发生发展的分子基础,本研究试图鉴定ESCC全基因组特征性改变,包括外显子突变和结构改变。还分析了这些基因改变的临床意义。对9对ESCC及其配对血液样本进行外显子组测序和验证,随后使用桑格测序法对其他样本进行验证。采用全基因组单核苷酸多态性(SNP)芯片检测55例样本中的拷贝数改变(CNA)和杂合性缺失(LOH),其中包括9例接受外显子组测序的ESCC样本。在9例患者中验证了102个基因中的108个非同义体细胞突变(NSSM)。在我们的基因本体(GO)分析中发现染色质修饰过程富集。TP53突变的肿瘤基因组比无TP53突变的肿瘤基因组明显更不稳定。在基因组改变格局方面,三分之二的病例发生了覆盖CDKN2A/2B的9p21.3缺失(30.9%)、覆盖CCND1的11q13.3扩增(30.9%)和TP53点突变(50.9%)。这些结果表明,细胞周期中G1期的失调是ESCC的关键事件。此外,发现6个最小共同区域在ESCC样本中显著改变,其中3个区域,即9p21.3、7p11.2和3p12.1,与淋巴结转移相关。鉴于ESCC中TP53突变与基因组不稳定性高度相关,CCND1的扩增、CDKN2A/2B的缺失以及TP53的体细胞突变似乎通过G1期失调发挥关键作用,因此有助于将这种癌症分为不同的基因组亚型。这些发现具有临床意义,可能对未来的分子诊断和治疗靶点有用。