Law F B F, Chen Y W, Wong K Y, Ying J, Tao Q, Langford C, Lee P Y, Law S, Cheung R W L, Chui C H, Tsao S W, Lam K Y, Wong J, Srivastava G, Tang J C O
Department of Pathology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
Oncogene. 2007 Aug 30;26(40):5877-88. doi: 10.1038/sj.onc.1210390. Epub 2007 Mar 26.
By comparative DNA fingerprinting, we identified a 357-bp DNA fragment frequently amplified in esophageal squamous cell carcinomas (ESCC). This fragment overlaps with an expressed sequence tag mapped to 7q22. Further 5' and 3'-rapid amplification of cDNA ends revealed that it is part of a novel, single-exon gene with full-length mRNA of 2052 bp and encodes a nuclear protein of 109 amino acids ( approximately 15 kDa). This gene, designated as gene amplified in esophageal cancer 1 (GAEC1), was located within a 1-2 Mb amplicon at 7q22.1 identified by high-resolution 1 Mb array-comparative genomic hybridization in 6/10 ESCC cell lines. GAEC1 was ubiquitously expressed in normal tissues including esophageal and gastrointestinal organs; with amplification and overexpression in 6/10 (60%) ESCC cell lines and 34/99 (34%) primary tumors. Overexpression of GAEC1 in 3T3 mouse fibroblasts caused foci formation and colony formation in soft agar, comparable to H-ras and injection of GAEC1-transfected 3T3 cells into athymic nude mice formed undifferentiated sarcoma in vivo, indicating that GAEC1 is a transforming oncogene. Although no significant correlation was observed between GAEC1 amplification and clinicopathological parameters and prognosis, our study demonstrated that overexpressed GAEC1 has tumorigenic potential and suggest that overexpressed GAEC1 may play an important role in ESCC pathogenesis.
通过比较DNA指纹图谱,我们在食管鳞状细胞癌(ESCC)中鉴定出一个经常扩增的357bp DNA片段。该片段与一个定位在7q22的表达序列标签重叠。进一步的5'和3'-cDNA末端快速扩增显示,它是一个新的单外显子基因的一部分,其全长mRNA为2052bp,编码一个109个氨基酸(约15kDa)的核蛋白。这个基因被命名为食管癌中扩增的基因1(GAEC1),位于7q22.1的一个1-2Mb扩增子内,该扩增子是通过高分辨率1Mb阵列比较基因组杂交在6/10的ESCC细胞系中鉴定出来的。GAEC1在包括食管和胃肠器官在内的正常组织中普遍表达;在6/10(60%)的ESCC细胞系和34/99(34%)的原发性肿瘤中存在扩增和过表达。GAEC1在3T3小鼠成纤维细胞中的过表达导致了集落形成和软琼脂中的克隆形成,类似于H-ras,并且将GAEC1转染的3T3细胞注射到无胸腺裸鼠体内会在体内形成未分化的肉瘤,这表明GAEC1是一个具有转化能力的致癌基因。虽然在GAEC1扩增与临床病理参数及预后之间未观察到显著相关性,但我们的研究表明,过表达的GAEC1具有致瘤潜力,并提示过表达的GAEC1可能在ESCC发病机制中起重要作用。