Identification 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
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, sin...
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Veröffentlicht in: | Oncogene 2007-08, Vol.26 (40), p.5877-5888 |
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Zusammenfassung: | 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 (∼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. |
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ISSN: | 0950-9232 1476-5594 |
DOI: | 10.1038/sj.onc.1210390 |