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Article: Significance of Id-1 up-regulation and its association with EGFR in bladder cancer cell invasion
Title | Significance of Id-1 up-regulation and its association with EGFR in bladder cancer cell invasion |
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Authors | |
Keywords | Bladder cancer Epidermal growth factor receptor Inhibitor of differentiation/DNA binding Invasion |
Issue Date | 2006 |
Publisher | Spandidos Publications. The Journal's web site is located at http://www.spandidos-publications.com/ijo/ |
Citation | International Journal Of Oncology, 2006, v. 28 n. 4, p. 847-854 How to Cite? |
Abstract | Epidermal growth factor receptor (EGFR) is suggested to be one of the positive factors in the invasive progression of bladder cancer. Id-1 (inhibitor of differentiation or DNA binding), a helix-loop-helix (HLH) transcription factor, was recently identified as a key factor in the EGFR signalling pathway. The aim of this study was to investigate the role of Id-1 in bladder cancer progression and its relationship with EGFR. Using clinical specimens from different stages of bladder cancer, immunohistochemical staining was performed to determine if Id-1 expression was positively associated with tumour staging and EGFR expression. The direct role of Id-1 in cancer cell invasion was also investigated through ectopically expressing the Id-1 gene in a RT112 bladder cancer cell line by wound closure and collagen invasion assays. To explore the therapeutic potential of targeting the Id-1 gene in the treatment of invasive bladder cancer, we studied if inactivation of the Id-1 gene through small RNA interference could lead to the suppression of invasion in a MGHU1 bladder cancer cell line. Our results showed that the up-regulation of Id-1 was associated with increased EGFR expression, clinical staging and the invasion ability of bladder cancer cells. Inactivation of Id-1 may be a potential therapeutic target to inhibit the invasion by bladder cancer cells. |
Persistent Identifier | http://hdl.handle.net/10722/67788 |
ISSN | 2023 Impact Factor: 4.5 2023 SCImago Journal Rankings: 1.099 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Ding, Y | en_HK |
dc.contributor.author | Wang, G | en_HK |
dc.contributor.author | Ling, MT | en_HK |
dc.contributor.author | Wong, YC | en_HK |
dc.contributor.author | Li, X | en_HK |
dc.contributor.author | Na, Y | en_HK |
dc.contributor.author | Zhang, X | en_HK |
dc.contributor.author | Chua, CW | en_HK |
dc.contributor.author | Wang, X | en_HK |
dc.contributor.author | Xin, D | en_HK |
dc.date.accessioned | 2010-09-06T05:58:15Z | - |
dc.date.available | 2010-09-06T05:58:15Z | - |
dc.date.issued | 2006 | en_HK |
dc.identifier.citation | International Journal Of Oncology, 2006, v. 28 n. 4, p. 847-854 | en_HK |
dc.identifier.issn | 1019-6439 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/67788 | - |
dc.description.abstract | Epidermal growth factor receptor (EGFR) is suggested to be one of the positive factors in the invasive progression of bladder cancer. Id-1 (inhibitor of differentiation or DNA binding), a helix-loop-helix (HLH) transcription factor, was recently identified as a key factor in the EGFR signalling pathway. The aim of this study was to investigate the role of Id-1 in bladder cancer progression and its relationship with EGFR. Using clinical specimens from different stages of bladder cancer, immunohistochemical staining was performed to determine if Id-1 expression was positively associated with tumour staging and EGFR expression. The direct role of Id-1 in cancer cell invasion was also investigated through ectopically expressing the Id-1 gene in a RT112 bladder cancer cell line by wound closure and collagen invasion assays. To explore the therapeutic potential of targeting the Id-1 gene in the treatment of invasive bladder cancer, we studied if inactivation of the Id-1 gene through small RNA interference could lead to the suppression of invasion in a MGHU1 bladder cancer cell line. Our results showed that the up-regulation of Id-1 was associated with increased EGFR expression, clinical staging and the invasion ability of bladder cancer cells. Inactivation of Id-1 may be a potential therapeutic target to inhibit the invasion by bladder cancer cells. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Spandidos Publications. The Journal's web site is located at http://www.spandidos-publications.com/ijo/ | en_HK |
dc.relation.ispartof | International Journal of Oncology | en_HK |
dc.subject | Bladder cancer | en_HK |
dc.subject | Epidermal growth factor receptor | en_HK |
dc.subject | Inhibitor of differentiation/DNA binding | en_HK |
dc.subject | Invasion | en_HK |
dc.subject.mesh | Inhibitor of Differentiation Protein 1 - analysis - genetics - physiology | - |
dc.subject.mesh | Genetic Vectors/genetics | - |
dc.subject.mesh | Neoplasm Staging | - |
dc.subject.mesh | Receptor, Epidermal Growth Factor - analysis - genetics | - |
dc.subject.mesh | Urinary Bladder Neoplasms - genetics - metabolism - pathology | - |
dc.title | Significance of Id-1 up-regulation and its association with EGFR in bladder cancer cell invasion | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1019-6439&volume=28&issue=4&spage=847&epage=854&date=2006&atitle=Significance+of+Id-1+up-regulation+and+its+association+with+EGFR+in+bladder+cancer+cell+invasion | en_HK |
dc.identifier.email | Ling, MT:patling@hkucc.hku.hk | en_HK |
dc.identifier.email | Wong, YC:ycwong@hkucc.hku.hk | en_HK |
dc.identifier.authority | Ling, MT=rp00449 | en_HK |
dc.identifier.authority | Wong, YC=rp00316 | en_HK |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.pmid | 16525633 | - |
dc.identifier.scopus | eid_2-s2.0-33744758656 | en_HK |
dc.identifier.hkuros | 138226 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-33744758656&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 28 | en_HK |
dc.identifier.issue | 4 | en_HK |
dc.identifier.spage | 847 | en_HK |
dc.identifier.epage | 854 | en_HK |
dc.identifier.isi | WOS:000236077500008 | - |
dc.publisher.place | Greece | en_HK |
dc.identifier.scopusauthorid | Ding, Y=36997788500 | en_HK |
dc.identifier.scopusauthorid | Wang, G=36683489600 | en_HK |
dc.identifier.scopusauthorid | Ling, MT=7102229780 | en_HK |
dc.identifier.scopusauthorid | Wong, YC=7403041798 | en_HK |
dc.identifier.scopusauthorid | Li, X=36065691100 | en_HK |
dc.identifier.scopusauthorid | Na, Y=7006088519 | en_HK |
dc.identifier.scopusauthorid | Zhang, X=36683620000 | en_HK |
dc.identifier.scopusauthorid | Chua, CW=9437494600 | en_HK |
dc.identifier.scopusauthorid | Wang, X=35335525600 | en_HK |
dc.identifier.scopusauthorid | Xin, D=7006327751 | en_HK |
dc.identifier.issnl | 1019-6439 | - |