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- Publisher Website: 10.1007/s00432-007-0230-0
- Scopus: eid_2-s2.0-35248824027
- PMID: 17497168
- WOS: WOS:000250063800003
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Article: Down-regulation of retinol binding protein 5 is associated with aggressive tumor features in hepatocellular carcinoma
Title | Down-regulation of retinol binding protein 5 is associated with aggressive tumor features in hepatocellular carcinoma |
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Authors | |
Keywords | Cellular retinol binding protein Prognosis |
Issue Date | 2007 |
Publisher | Springer Verlag. The Journal's web site is located at http://link.springer.de/link/service/journals/00432/index.htm |
Citation | Journal Of Cancer Research And Clinical Oncology, 2007, v. 133 n. 12, p. 929-936 How to Cite? |
Abstract | Purpose: Acyclic retinoid (ACR) has been shown to be a promising chemopreventive agent for hepatocellular carcinoma (HCC) after curative resection. The effects of retinoid are mediated by retinol-binding proteins (RBPs) through regulating cell proliferation and differentiation. Patients and methods: This study investigated the clinical significance of RBP5 in HCC. RBP5 mRNA level was examined by real-time quantitative PCR on 52 matched tumor and adjacent non-tumor liver tissues, and on ten normal livers. Expression of RBP5 protein was examined using Western blotting analysis and immunohistochemistry. Results: Down-regulation of RBP5 was found in HCC tissues at both mRNA and protein levels. Decreased RBP5 level was closely related to poor differentiation (P = 0.02) and large tumor size (P = 0.01). Low level of RPB5 was associated with poor overall survival (P = 0.02), and was an independent prognostic factor for HCC. Conclusions: Our study revealed that RBP5 down-regulation in HCC was associated with aggressive tumor features, suggesting an important role of RPB5 in HCC progression. © 2007 Springer-Verlag. |
Persistent Identifier | http://hdl.handle.net/10722/88803 |
ISSN | 2023 Impact Factor: 2.7 2023 SCImago Journal Rankings: 1.023 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Ho, JCY | en_HK |
dc.contributor.author | Cheung, ST | en_HK |
dc.contributor.author | Poon, WS | en_HK |
dc.contributor.author | Lee, YT | en_HK |
dc.contributor.author | Ng, IOL | en_HK |
dc.contributor.author | Fan, ST | en_HK |
dc.date.accessioned | 2010-09-06T09:48:12Z | - |
dc.date.available | 2010-09-06T09:48:12Z | - |
dc.date.issued | 2007 | en_HK |
dc.identifier.citation | Journal Of Cancer Research And Clinical Oncology, 2007, v. 133 n. 12, p. 929-936 | en_HK |
dc.identifier.issn | 0171-5216 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/88803 | - |
dc.description.abstract | Purpose: Acyclic retinoid (ACR) has been shown to be a promising chemopreventive agent for hepatocellular carcinoma (HCC) after curative resection. The effects of retinoid are mediated by retinol-binding proteins (RBPs) through regulating cell proliferation and differentiation. Patients and methods: This study investigated the clinical significance of RBP5 in HCC. RBP5 mRNA level was examined by real-time quantitative PCR on 52 matched tumor and adjacent non-tumor liver tissues, and on ten normal livers. Expression of RBP5 protein was examined using Western blotting analysis and immunohistochemistry. Results: Down-regulation of RBP5 was found in HCC tissues at both mRNA and protein levels. Decreased RBP5 level was closely related to poor differentiation (P = 0.02) and large tumor size (P = 0.01). Low level of RPB5 was associated with poor overall survival (P = 0.02), and was an independent prognostic factor for HCC. Conclusions: Our study revealed that RBP5 down-regulation in HCC was associated with aggressive tumor features, suggesting an important role of RPB5 in HCC progression. © 2007 Springer-Verlag. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Springer Verlag. The Journal's web site is located at http://link.springer.de/link/service/journals/00432/index.htm | en_HK |
dc.relation.ispartof | Journal of Cancer Research and Clinical Oncology | en_HK |
dc.subject | Cellular retinol binding protein | en_HK |
dc.subject | Prognosis | en_HK |
dc.subject.mesh | Carcinoma, Hepatocellular - genetics - metabolism - mortality | en_HK |
dc.subject.mesh | Disease Progression | en_HK |
dc.subject.mesh | Down-Regulation | en_HK |
dc.subject.mesh | Female | en_HK |
dc.subject.mesh | Gene Expression Regulation, Neoplastic | en_HK |
dc.subject.mesh | Humans | en_HK |
dc.subject.mesh | Immunohistochemistry | en_HK |
dc.subject.mesh | Liver | en_HK |
dc.subject.mesh | Liver Neoplasms - genetics - metabolism - mortality | en_HK |
dc.subject.mesh | Male | en_HK |
dc.subject.mesh | Middle Aged | en_HK |
dc.subject.mesh | RNA, Messenger - metabolism | en_HK |
dc.subject.mesh | Retinol-Binding Proteins - metabolism | en_HK |
dc.subject.mesh | Retinol-Binding Proteins, Cellular - metabolism | en_HK |
dc.subject.mesh | Reverse Transcriptase Polymerase Chain Reaction | en_HK |
dc.subject.mesh | Survival Analysis | en_HK |
dc.title | Down-regulation of retinol binding protein 5 is associated with aggressive tumor features in hepatocellular carcinoma | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0171-5216&volume=133&issue=12&spage=929&epage=936&date=2007&atitle=Down-regulation+of+retinol+binding+protein+5+is+associated+with+aggressive+tumor+features+in+hepatocellular+carcinoma | en_HK |
dc.identifier.email | Cheung, ST: stcheung@hkucc.hku.hk | en_HK |
dc.identifier.email | Ng, IOL: iolng@hkucc.hku.hk | en_HK |
dc.identifier.email | Fan, ST: stfan@hku.hk | en_HK |
dc.identifier.authority | Cheung, ST=rp00457 | en_HK |
dc.identifier.authority | Ng, IOL=rp00335 | en_HK |
dc.identifier.authority | Fan, ST=rp00355 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1007/s00432-007-0230-0 | en_HK |
dc.identifier.pmid | 17497168 | - |
dc.identifier.scopus | eid_2-s2.0-35248824027 | en_HK |
dc.identifier.hkuros | 140967 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-35248824027&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 133 | en_HK |
dc.identifier.issue | 12 | en_HK |
dc.identifier.spage | 929 | en_HK |
dc.identifier.epage | 936 | en_HK |
dc.identifier.isi | WOS:000250063800003 | - |
dc.publisher.place | Germany | en_HK |
dc.identifier.scopusauthorid | Ho, JCY=7402650284 | en_HK |
dc.identifier.scopusauthorid | Cheung, ST=7202473497 | en_HK |
dc.identifier.scopusauthorid | Poon, WS=35082584500 | en_HK |
dc.identifier.scopusauthorid | Lee, YT=22734702300 | en_HK |
dc.identifier.scopusauthorid | Ng, IOL=7102753722 | en_HK |
dc.identifier.scopusauthorid | Fan, ST=7402678224 | en_HK |
dc.identifier.issnl | 0171-5216 | - |