Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/17076
Title: Identifcation of a novel tumor transforming gene GAEC1 at 7q22 which encodes a nuclear protein and is frequently amplified and overexpressed in esophageal squamous cell carcinoma
Authors: Law, FBF
Chen, YW
Wong, KY
Ying, J
Tao, Q
Langford, C
Lee, PY
Law, S
Cheung, RWL
Chui, CH
Tsao, SW
Lam, KY
Wong, J
Srivastava, G
Tang, JCO 
Keywords: Gene amplifcation
Overexpression
Transforming gene
Esophageal cancer
7q22
Issue Date: 2007
Publisher: Nature Publishing Group
Source: Oncogene, 2007, v. 26, no. 40, p. 5877-5888 How to cite?
Journal: Oncogene 
Abstract: 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 ( similar to 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. broblasts 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.
URI: http://hdl.handle.net/10397/17076
ISSN: 0950-9232
DOI: 10.1038/sj.onc.1210390
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