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- Publisher Website: 10.1016/j.canlet.2005.12.030
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Article: SRC-3/AIB1 protein and gene amplification levels in human esophageal squamous cell carcinomas
Title | SRC-3/AIB1 protein and gene amplification levels in human esophageal squamous cell carcinomas |
---|---|
Authors | |
Keywords | Amplification Esophageal squamous cell carcinoma Immunohistochemistry SRC-3 Tissue microarray |
Issue Date | 2007 |
Publisher | Elsevier Ireland Ltd. The Journal's web site is located at http://www.elsevier.com/locate/canlet |
Citation | Cancer Letters, 2007, v. 245 n. 1-2, p. 69-74 How to Cite? |
Abstract | It has been suggested that the steroid receptor coactivatior-3 (SRC-3) gene, also known as AIB1, ACTR, RAC3, p/CIP and TRAM-1, located at 20q12, plays an oncogenic role in several types of human cancers. In this study, we examined the encoded protein expression of SRC-3 and its copy number in 221 human esophageal squamous cell carcinomas (ESCCs). In this ESCC series, the overexpression and increased copy number of SRC-3 gene was detected in 46 and 13% of ESCCs, respectively. In addition, overexpression of SRC-3 was observed more frequently in primary ESCCs in late T stages (T3/T4) than that in earlier T1/T2 stages (P<0.05), but no significant association of expression of SRC-3 and status of lymph node metastases was observed (P>0.05). These results suggest that overexpression of SRC-3, caused by gene amplification/gain or other molecular mechanisms, might provide a selective advantage for the development and local invasion of certain subsets of ESCC. In addition, a significant correlation (P<0.05) of overexpression of SRC-3 with increased cell proliferation (through detection of Ki-67 expression) was observed in these ESCCs. These findings suggest a potential role of SRC-3 in the control of ESCC cell proliferation; such may be responsible, at least in part, for tumorigenesis and/or progression of ESCC. © 2006 Elsevier Ireland Ltd. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/72006 |
ISSN | 2023 Impact Factor: 9.1 2023 SCImago Journal Rankings: 2.595 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Xu, FP | en_HK |
dc.contributor.author | Xie, D | en_HK |
dc.contributor.author | Wen, JM | en_HK |
dc.contributor.author | Wu, HX | en_HK |
dc.contributor.author | Liu, YD | en_HK |
dc.contributor.author | Bi, J | en_HK |
dc.contributor.author | Lv, ZL | en_HK |
dc.contributor.author | Zeng, YX | en_HK |
dc.contributor.author | Guan, XY | en_HK |
dc.date.accessioned | 2010-09-06T06:37:25Z | - |
dc.date.available | 2010-09-06T06:37:25Z | - |
dc.date.issued | 2007 | en_HK |
dc.identifier.citation | Cancer Letters, 2007, v. 245 n. 1-2, p. 69-74 | en_HK |
dc.identifier.issn | 0304-3835 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/72006 | - |
dc.description.abstract | It has been suggested that the steroid receptor coactivatior-3 (SRC-3) gene, also known as AIB1, ACTR, RAC3, p/CIP and TRAM-1, located at 20q12, plays an oncogenic role in several types of human cancers. In this study, we examined the encoded protein expression of SRC-3 and its copy number in 221 human esophageal squamous cell carcinomas (ESCCs). In this ESCC series, the overexpression and increased copy number of SRC-3 gene was detected in 46 and 13% of ESCCs, respectively. In addition, overexpression of SRC-3 was observed more frequently in primary ESCCs in late T stages (T3/T4) than that in earlier T1/T2 stages (P<0.05), but no significant association of expression of SRC-3 and status of lymph node metastases was observed (P>0.05). These results suggest that overexpression of SRC-3, caused by gene amplification/gain or other molecular mechanisms, might provide a selective advantage for the development and local invasion of certain subsets of ESCC. In addition, a significant correlation (P<0.05) of overexpression of SRC-3 with increased cell proliferation (through detection of Ki-67 expression) was observed in these ESCCs. These findings suggest a potential role of SRC-3 in the control of ESCC cell proliferation; such may be responsible, at least in part, for tumorigenesis and/or progression of ESCC. © 2006 Elsevier Ireland Ltd. All rights reserved. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Elsevier Ireland Ltd. The Journal's web site is located at http://www.elsevier.com/locate/canlet | en_HK |
dc.relation.ispartof | Cancer Letters | en_HK |
dc.rights | Cancer Letters. Copyright © Elsevier Ireland Ltd. | en_HK |
dc.subject | Amplification | - |
dc.subject | Esophageal squamous cell carcinoma | - |
dc.subject | Immunohistochemistry | - |
dc.subject | SRC-3 | - |
dc.subject | Tissue microarray | - |
dc.subject.mesh | Adult | en_HK |
dc.subject.mesh | Aged | en_HK |
dc.subject.mesh | Carcinoma, Squamous Cell - genetics - metabolism - pathology | en_HK |
dc.subject.mesh | Cell Proliferation | en_HK |
dc.subject.mesh | Esophageal Neoplasms - genetics - metabolism - pathology | en_HK |
dc.subject.mesh | Female | en_HK |
dc.subject.mesh | Gene Amplification | en_HK |
dc.subject.mesh | Gene Dosage | en_HK |
dc.subject.mesh | Histone Acetyltransferases - analysis - genetics | en_HK |
dc.subject.mesh | Humans | en_HK |
dc.subject.mesh | Immunohistochemistry | en_HK |
dc.subject.mesh | In Situ Hybridization, Fluorescence | en_HK |
dc.subject.mesh | Ki-67 Antigen - analysis | en_HK |
dc.subject.mesh | Male | en_HK |
dc.subject.mesh | Middle Aged | en_HK |
dc.subject.mesh | Nuclear Receptor Coactivator 3 | en_HK |
dc.subject.mesh | Tissue Array Analysis | en_HK |
dc.subject.mesh | Trans-Activators - analysis - genetics | en_HK |
dc.title | SRC-3/AIB1 protein and gene amplification levels in human esophageal squamous cell carcinomas | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0304-3835&volume=245&spage=69&epage=74&date=2007&atitle=SRC-3/AIB1+protein+and+gene+amplification+levels+in+human+esophageal+squamous+cell+carcinomas. | en_HK |
dc.identifier.email | Guan, XY:xyguan@hkucc.hku.hk | en_HK |
dc.identifier.authority | Guan, XY=rp00454 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.canlet.2005.12.030 | en_HK |
dc.identifier.pmid | 16458427 | - |
dc.identifier.scopus | eid_2-s2.0-33845651685 | en_HK |
dc.identifier.hkuros | 133764 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-33845651685&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 245 | en_HK |
dc.identifier.issue | 1-2 | en_HK |
dc.identifier.spage | 69 | en_HK |
dc.identifier.epage | 74 | en_HK |
dc.identifier.isi | WOS:000244146100008 | - |
dc.publisher.place | Ireland | en_HK |
dc.identifier.scopusauthorid | Xu, FP=12647094900 | en_HK |
dc.identifier.scopusauthorid | Xie, D=35070710200 | en_HK |
dc.identifier.scopusauthorid | Wen, JM=49762409100 | en_HK |
dc.identifier.scopusauthorid | Wu, HX=36189521500 | en_HK |
dc.identifier.scopusauthorid | Liu, YD=49761904800 | en_HK |
dc.identifier.scopusauthorid | Bi, J=7103093361 | en_HK |
dc.identifier.scopusauthorid | Lv, ZL=49761909800 | en_HK |
dc.identifier.scopusauthorid | Zeng, YX=7402981579 | en_HK |
dc.identifier.scopusauthorid | Guan, XY=7201463221 | en_HK |
dc.identifier.issnl | 0304-3835 | - |