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- Publisher Website: 10.1111/j.1365-2559.2007.02637.x
- Scopus: eid_2-s2.0-33847289707
- PMID: 17448024
- WOS: WOS:000244518600010
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Article: Prognostic significance of Id-1 and its association with EGFR in renal cell cancer
Title | Prognostic significance of Id-1 and its association with EGFR in renal cell cancer |
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Authors | |
Keywords | EGFR Id-1 Immunohistochemistry Microarray Renal cell cancer |
Issue Date | 2007 |
Publisher | Blackwell Publishing Ltd. The Journal's web site is located at http://www.blackwellpublishing.com/journals/HIS |
Citation | Histopathology, 2007, v. 50 n. 4, p. 484-490 How to Cite? |
Abstract | Aims: Epidermal growth factor receptor (EGFR) is suggested as one of the positive regulators in the invasive progression of renal cell cancer (RCC). Recently, Id-1 (inhibitor of differentiation or DNA binding), a helix-loop-helix transcription factor, has been identified as one of the key factors in the EGFR signalling pathway. The aim of this study was to investigate the significance of Id-1 expression in renal cell cancer and to study its relationship with EGFR. Methods and results: Id-1 and EGFR expression was examined in tissue microarray (TMA) samples of 107 RCC and 32 normal kidney specimens by immunohistochemistry. Relative Id-1 and EGFR protein expression was quantified by estimating the staining intensity on a four-grade scale. We found that while negative to weak expression of Id-1 and EGFR was observed in non-malignant kidney tissues, most RCCs showed significant positive Id-1 and EGFR expression in tumour cells. In addition, Id-1 immunostaining intensity was positively associated with increased tumour staging, grading and EGFR expression. Conclusion: Overexpression of Id-1 is a novel marker for advanced RCC which is positively correlated with EGFR expression. Our results suggest that Id-1 may play an important role in the development of RCC and indicate that Id-1 is a potential marker of patients with a poor prognosis. © 2007 The Authors. |
Persistent Identifier | http://hdl.handle.net/10722/67483 |
ISSN | 2023 Impact Factor: 3.9 2023 SCImago Journal Rankings: 1.392 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Li, X | en_HK |
dc.contributor.author | Zhang | en_HK |
dc.contributor.author | Xin, D | en_HK |
dc.contributor.author | Chua, CW | en_HK |
dc.contributor.author | Wong, YC | en_HK |
dc.contributor.author | Leung, SCL | en_HK |
dc.contributor.author | Na, Y | en_HK |
dc.contributor.author | Wang, X | en_HK |
dc.date.accessioned | 2010-09-06T05:55:32Z | - |
dc.date.available | 2010-09-06T05:55:32Z | - |
dc.date.issued | 2007 | en_HK |
dc.identifier.citation | Histopathology, 2007, v. 50 n. 4, p. 484-490 | en_HK |
dc.identifier.issn | 0309-0167 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/67483 | - |
dc.description.abstract | Aims: Epidermal growth factor receptor (EGFR) is suggested as one of the positive regulators in the invasive progression of renal cell cancer (RCC). Recently, Id-1 (inhibitor of differentiation or DNA binding), a helix-loop-helix transcription factor, has been identified as one of the key factors in the EGFR signalling pathway. The aim of this study was to investigate the significance of Id-1 expression in renal cell cancer and to study its relationship with EGFR. Methods and results: Id-1 and EGFR expression was examined in tissue microarray (TMA) samples of 107 RCC and 32 normal kidney specimens by immunohistochemistry. Relative Id-1 and EGFR protein expression was quantified by estimating the staining intensity on a four-grade scale. We found that while negative to weak expression of Id-1 and EGFR was observed in non-malignant kidney tissues, most RCCs showed significant positive Id-1 and EGFR expression in tumour cells. In addition, Id-1 immunostaining intensity was positively associated with increased tumour staging, grading and EGFR expression. Conclusion: Overexpression of Id-1 is a novel marker for advanced RCC which is positively correlated with EGFR expression. Our results suggest that Id-1 may play an important role in the development of RCC and indicate that Id-1 is a potential marker of patients with a poor prognosis. © 2007 The Authors. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Blackwell Publishing Ltd. The Journal's web site is located at http://www.blackwellpublishing.com/journals/HIS | en_HK |
dc.relation.ispartof | Histopathology | en_HK |
dc.rights | Histopathology. Copyright © Blackwell Publishing Ltd. | en_HK |
dc.subject | EGFR | - |
dc.subject | Id-1 | - |
dc.subject | Immunohistochemistry | - |
dc.subject | Microarray | - |
dc.subject | Renal cell cancer | - |
dc.subject.mesh | Adult | en_HK |
dc.subject.mesh | Aged | en_HK |
dc.subject.mesh | Aged, 80 and over | en_HK |
dc.subject.mesh | Carcinoma, Renal Cell - metabolism - pathology | en_HK |
dc.subject.mesh | Female | en_HK |
dc.subject.mesh | Humans | en_HK |
dc.subject.mesh | Immunohistochemistry | en_HK |
dc.subject.mesh | Inhibitor of Differentiation Protein 1 - biosynthesis | en_HK |
dc.subject.mesh | Kidney - metabolism - pathology | en_HK |
dc.subject.mesh | Kidney Neoplasms - metabolism - pathology | en_HK |
dc.subject.mesh | Male | en_HK |
dc.subject.mesh | Middle Aged | en_HK |
dc.subject.mesh | Neoplasm Invasiveness | en_HK |
dc.subject.mesh | Receptor, Epidermal Growth Factor - physiology | en_HK |
dc.subject.mesh | Reference Values | en_HK |
dc.subject.mesh | Tissue Array Analysis | en_HK |
dc.title | Prognostic significance of Id-1 and its association with EGFR in renal cell cancer | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0309-0167&volume=50&spage=484&epage=490&date=2007&atitle=Prognostic+significance+of+Id-1+and+its+association+with+EGFR+in+renal+cell+cancer | en_HK |
dc.identifier.email | Wong, YC:ycwong@hkucc.hku.hk | en_HK |
dc.identifier.authority | Wong, YC=rp00316 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1111/j.1365-2559.2007.02637.x | en_HK |
dc.identifier.pmid | 17448024 | - |
dc.identifier.scopus | eid_2-s2.0-33847289707 | en_HK |
dc.identifier.hkuros | 147309 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-33847289707&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 50 | en_HK |
dc.identifier.issue | 4 | en_HK |
dc.identifier.spage | 484 | en_HK |
dc.identifier.epage | 490 | en_HK |
dc.identifier.isi | WOS:000244518600010 | - |
dc.publisher.place | United Kingdom | en_HK |
dc.identifier.scopusauthorid | Li, X=36072733900 | en_HK |
dc.identifier.scopusauthorid | Zhang=16023302600 | en_HK |
dc.identifier.scopusauthorid | Xin, D=7006327751 | en_HK |
dc.identifier.scopusauthorid | Chua, CW=9437494600 | en_HK |
dc.identifier.scopusauthorid | Wong, YC=7403041798 | en_HK |
dc.identifier.scopusauthorid | Leung, SCL=36894169100 | en_HK |
dc.identifier.scopusauthorid | Na, Y=7006088519 | en_HK |
dc.identifier.scopusauthorid | Wang, X=7501854829 | en_HK |
dc.identifier.citeulike | 1136781 | - |
dc.identifier.issnl | 0309-0167 | - |