Identification of candidate target genes of genomic aberrations in esophageal squamous cell carcinoma
Identification of candidate target genes of genomic aberrations in esophageal squamous cell carcinoma
复制标题
食管鳞状细胞癌基因组畸变候选靶基因的鉴定。
DOI:
10.3892/ol.2016.4947
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发表时间:
2016-10-01
期刊:
影响因子:
2.9
通讯作者:
Shi, Zhi-Zhou
中科院分区:
文献类型:
--
作者:
Shen, Tian-Yun;Mei, Li-Li;Shi, Zhi-Zhou
The aim of the present study was to identify the candidate target genes of genomic aberrations in esophageal squamous cell carcinoma (ESCC). Array comparative genomic hybridization (CGH) and quantitative polymerase chain reaction were applied to analyze the copy number changes and expression level of candidate genes, respectively. Integrative analysis revealed that homozygous deletions of cyclin-dependent kinase inhibitor (CDKN) 2A and CDKN2B and gains of fascin actin-bundling protein 1 (FSCN1) and homer scaffolding protein 3 (HOMER3) occurred frequently in ESCC. The results demonstrated that the homozygous deletion of CDKN2A or CDKN2B was significantly associated with lymph node metastasis. Notably, the expression of CDKN2A and CDKN2B was lower in dysplasia than in normal esophageal epithelium. We also observed that the copy number increase of FSCN1 was significantly associated with pT, pN and pStage, and that the gain of HOMER3 was significantly linked with pN and pStage. We further revealed that FSCN1 and HOMER3 were overexpressed in ESCC, and that their overexpression was correlated with copy number increase. In conclusion, CDKN2A, CDKN2B, FSCN1 and HOMER3 are candidate cancer-associated genes and may play a tumorigenic role in ESCC.