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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container_title | Oncogene |
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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 |
format | Article |
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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.</description><identifier>ISSN: 0950-9232</identifier><identifier>EISSN: 1476-5594</identifier><identifier>DOI: 10.1038/sj.onc.1210390</identifier><identifier>PMID: 17384685</identifier><identifier>CODEN: ONCNES</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>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</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&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). 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.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Apoptosis</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Cancer</subject><subject>Carcinoma, Squamous Cell - genetics</subject><subject>Carcinoma, Squamous Cell - metabolism</subject><subject>Cell Biology</subject><subject>Cell Line, Tumor</subject><subject>Cell Nucleus - metabolism</subject><subject>Cell physiology</subject><subject>Cell transformation and carcinogenesis. Action of oncogenes and antioncogenes</subject><subject>Cellular proteins</subject><subject>Chromosome 7</subject><subject>Chromosomes, Human, Pair 7</subject><subject>Diagnosis</subject><subject>DNA fingerprinting</subject><subject>DNA fingerprints</subject><subject>DNA testing</subject><subject>Esophageal cancer</subject><subject>Esophageal carcinoma</subject><subject>Esophageal Neoplasms - genetics</subject><subject>Esophageal Neoplasms - metabolism</subject><subject>Esophagus</subject><subject>Expressed sequence tags</subject><subject>Fibroblasts</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Gene expression</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Genetic aspects</subject><subject>Genomics</subject><subject>H-Ras protein</subject><subject>Human Genetics</subject><subject>Humans</subject><subject>Hybridization</subject><subject>Internal Medicine</subject><subject>Medical sciences</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Mice</subject><subject>Mice, Nude</subject><subject>Models, Genetic</subject><subject>Molecular and cellular biology</subject><subject>Molecular Sequence Data</subject><subject>mRNA</subject><subject>Neoplasm Transplantation</subject><subject>Nuclear Proteins - biosynthesis</subject><subject>Nuclear Proteins - genetics</subject><subject>Oncology</subject><subject>original-article</subject><subject>Physiological aspects</subject><subject>Proteins</subject><subject>Rodents</subject><subject>Sarcoma</subject><subject>Squamous cell carcinoma</subject><subject>Tumors</subject><issn>0950-9232</issn><issn>1476-5594</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFkk1rGzEQhpfS0rhprz0W0ZLe7OhrtdqjMUkaCPSS-yJrR7bMrmRLu03zu_oHO04WDCWh6CCkeUbvzOgtis-MLhgV-jLvFjHYBeN4qumbYsZkpeZlWcu3xYzWJZ3XXPCz4kPOO0ppVVP-vjhjldBS6XJW_LltIQzeeWsGHwOJjhgS4i_oyDD2MZEhmZBdTL0PG7KBAORmebVixAykOnBOHrbebgkEG1vIx9zRdmAS2ac4gA_EhJb4TFyCw4hK3SMx_b5DQWifYiiV4Pc-Qc54gwmQ435rNmA6kg-j6eOYiYWuI9Yk60PszcfinTNdhk_Tfl7cX1_dr37M737e3K6Wd3NbiorOHQ7FKkprp6Qx1KrSqNoZ5aRQOAfHBGVKtqCtFmsrK01dVYNZt1pbp4Q4L74_P4utYO15aHqfj5WYAFhUozRnFeXlf0FWV1IyzhH89g-4i2MK2EPDlWSiklRTpL6-SvFKlFw_aU5PbUwHjQ8u4kfZo26zZFoxbI7WSC1eoHC10HsbAziP9y8l2BRzTuCaffK9SY8No83RcE3eNWi4ZjIcJnyZih3XPbQnfHIYAhcTYLI1nUM7WZ9PXE0lFVQhd_nMZQyFDaRT169I_wVY4-3_</recordid><startdate>20070830</startdate><enddate>20070830</enddate><creator>Law, F B F</creator><creator>Chen, Y W</creator><creator>Wong, K Y</creator><creator>Ying, J</creator><creator>Tao, Q</creator><creator>Langford, C</creator><creator>Lee, P Y</creator><creator>Law, S</creator><creator>Cheung, R W L</creator><creator>Chui, C H</creator><creator>Tsao, S W</creator><creator>Lam, K Y</creator><creator>Wong, J</creator><creator>Srivastava, G</creator><creator>Tang, J C O</creator><general>Nature Publishing Group UK</general><general>Nature Publishing</general><general>Nature Publishing Group</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20070830</creationdate><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><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5370-f121c6009f64aa0c65a69fa6f436790f130164de8c83bc4780f79eabd88cf633</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Apoptosis</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Cancer</topic><topic>Carcinoma, Squamous Cell - genetics</topic><topic>Carcinoma, Squamous Cell - metabolism</topic><topic>Cell Biology</topic><topic>Cell Line, Tumor</topic><topic>Cell Nucleus - metabolism</topic><topic>Cell physiology</topic><topic>Cell transformation and carcinogenesis. Action of oncogenes and antioncogenes</topic><topic>Cellular proteins</topic><topic>Chromosome 7</topic><topic>Chromosomes, Human, Pair 7</topic><topic>Diagnosis</topic><topic>DNA fingerprinting</topic><topic>DNA fingerprints</topic><topic>DNA testing</topic><topic>Esophageal cancer</topic><topic>Esophageal carcinoma</topic><topic>Esophageal Neoplasms - genetics</topic><topic>Esophageal Neoplasms - metabolism</topic><topic>Esophagus</topic><topic>Expressed sequence tags</topic><topic>Fibroblasts</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Gene expression</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Genetic aspects</topic><topic>Genomics</topic><topic>H-Ras protein</topic><topic>Human Genetics</topic><topic>Humans</topic><topic>Hybridization</topic><topic>Internal Medicine</topic><topic>Medical sciences</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Mice</topic><topic>Mice, Nude</topic><topic>Models, Genetic</topic><topic>Molecular and cellular biology</topic><topic>Molecular Sequence Data</topic><topic>mRNA</topic><topic>Neoplasm Transplantation</topic><topic>Nuclear Proteins - biosynthesis</topic><topic>Nuclear Proteins - genetics</topic><topic>Oncology</topic><topic>original-article</topic><topic>Physiological aspects</topic><topic>Proteins</topic><topic>Rodents</topic><topic>Sarcoma</topic><topic>Squamous cell carcinoma</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Oncogene</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Law, F B F</au><au>Chen, Y W</au><au>Wong, K Y</au><au>Ying, J</au><au>Tao, Q</au><au>Langford, C</au><au>Lee, P Y</au><au>Law, S</au><au>Cheung, R W L</au><au>Chui, C H</au><au>Tsao, S W</au><au>Lam, K Y</au><au>Wong, J</au><au>Srivastava, G</au><au>Tang, J C O</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>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</atitle><jtitle>Oncogene</jtitle><stitle>Oncogene</stitle><addtitle>Oncogene</addtitle><date>2007-08-30</date><risdate>2007</risdate><volume>26</volume><issue>40</issue><spage>5877</spage><epage>5888</epage><pages>5877-5888</pages><issn>0950-9232</issn><eissn>1476-5594</eissn><coden>ONCNES</coden><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 (∼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.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>17384685</pmid><doi>10.1038/sj.onc.1210390</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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ispartof | Oncogene, 2007-08, Vol.26 (40), p.5877-5888 |
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language | eng |
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source | MEDLINE; Springer Nature - Complete Springer Journals; Nature Journals Online; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
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 |
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