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
Hauptverfasser: 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
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container_end_page 5888
container_issue 40
container_start_page 5877
container_title Oncogene
container_volume 26
creator 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
description 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.
doi_str_mv 10.1038/sj.onc.1210390
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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. 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Action of oncogenes and antioncogenes ; Cellular proteins ; Chromosome 7 ; Chromosomes, Human, Pair 7 ; Diagnosis ; DNA fingerprinting ; DNA fingerprints ; DNA testing ; Esophageal cancer ; Esophageal carcinoma ; Esophageal Neoplasms - genetics ; Esophageal Neoplasms - metabolism ; Esophagus ; Expressed sequence tags ; Fibroblasts ; Fundamental and applied biological sciences. Psychology ; Gastroenterology. Liver. Pancreas. Abdomen ; Gene expression ; Gene Expression Regulation, Neoplastic ; Genetic aspects ; Genomics ; H-Ras protein ; Human Genetics ; Humans ; Hybridization ; Internal Medicine ; Medical sciences ; Medicine ; Medicine &amp; Public Health ; Mice ; Mice, Nude ; Models, Genetic ; Molecular and cellular biology ; Molecular Sequence Data ; mRNA ; Neoplasm Transplantation ; Nuclear Proteins - biosynthesis ; Nuclear Proteins - genetics ; Oncology ; original-article ; Physiological aspects ; Proteins ; Rodents ; Sarcoma ; Squamous cell carcinoma ; Tumors</subject><ispartof>Oncogene, 2007-08, Vol.26 (40), p.5877-5888</ispartof><rights>Springer Nature Limited 2007</rights><rights>2007 INIST-CNRS</rights><rights>COPYRIGHT 2007 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Aug 30, 2007</rights><rights>Nature Publishing Group 2007.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5370-f121c6009f64aa0c65a69fa6f436790f130164de8c83bc4780f79eabd88cf633</citedby><cites>FETCH-LOGICAL-c5370-f121c6009f64aa0c65a69fa6f436790f130164de8c83bc4780f79eabd88cf633</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/sj.onc.1210390$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/sj.onc.1210390$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=19040306$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17384685$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Law, F B F</creatorcontrib><creatorcontrib>Chen, Y W</creatorcontrib><creatorcontrib>Wong, K Y</creatorcontrib><creatorcontrib>Ying, J</creatorcontrib><creatorcontrib>Tao, Q</creatorcontrib><creatorcontrib>Langford, C</creatorcontrib><creatorcontrib>Lee, P Y</creatorcontrib><creatorcontrib>Law, S</creatorcontrib><creatorcontrib>Cheung, R W L</creatorcontrib><creatorcontrib>Chui, C H</creatorcontrib><creatorcontrib>Tsao, S W</creatorcontrib><creatorcontrib>Lam, K Y</creatorcontrib><creatorcontrib>Wong, J</creatorcontrib><creatorcontrib>Srivastava, G</creatorcontrib><creatorcontrib>Tang, J C O</creatorcontrib><title>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</title><title>Oncogene</title><addtitle>Oncogene</addtitle><addtitle>Oncogene</addtitle><description>By comparative DNA fingerprinting, we identified a 357-bp DNA fragment frequently amplified in esophageal squamous cell carcinomas (ESCC). 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subjects Amino Acid Sequence
Animals
Apoptosis
Base Sequence
Biological and medical sciences
Cancer
Carcinoma, Squamous Cell - genetics
Carcinoma, Squamous Cell - metabolism
Cell Biology
Cell Line, Tumor
Cell Nucleus - metabolism
Cell physiology
Cell transformation and carcinogenesis. Action of oncogenes and antioncogenes
Cellular proteins
Chromosome 7
Chromosomes, Human, Pair 7
Diagnosis
DNA fingerprinting
DNA fingerprints
DNA testing
Esophageal cancer
Esophageal carcinoma
Esophageal Neoplasms - genetics
Esophageal Neoplasms - metabolism
Esophagus
Expressed sequence tags
Fibroblasts
Fundamental and applied biological sciences. Psychology
Gastroenterology. Liver. Pancreas. Abdomen
Gene expression
Gene Expression Regulation, Neoplastic
Genetic aspects
Genomics
H-Ras protein
Human Genetics
Humans
Hybridization
Internal Medicine
Medical sciences
Medicine
Medicine & Public Health
Mice
Mice, Nude
Models, Genetic
Molecular and cellular biology
Molecular Sequence Data
mRNA
Neoplasm Transplantation
Nuclear Proteins - biosynthesis
Nuclear Proteins - genetics
Oncology
original-article
Physiological aspects
Proteins
Rodents
Sarcoma
Squamous cell carcinoma
Tumors
title 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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-30T14%3A06%3A33IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Identification%20of%20a%20novel%20tumor%20transforming%20gene%20GAEC1%20at%207q22%20which%20encodes%20a%20nuclear%20protein%20and%20is%20frequently%20amplified%20and%20overexpressed%20in%20esophageal%20squamous%20cell%20carcinoma&rft.jtitle=Oncogene&rft.au=Law,%20F%20B%20F&rft.date=2007-08-30&rft.volume=26&rft.issue=40&rft.spage=5877&rft.epage=5888&rft.pages=5877-5888&rft.issn=0950-9232&rft.eissn=1476-5594&rft.coden=ONCNES&rft_id=info:doi/10.1038/sj.onc.1210390&rft_dat=%3Cgale_proqu%3EA186113009%3C/gale_proqu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=227352825&rft_id=info:pmid/17384685&rft_galeid=A186113009&rfr_iscdi=true