File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1002/ijc.22005
- Scopus: eid_2-s2.0-33747495216
- PMID: 16642471
- WOS: WOS:000239877200016
- Find via
Supplementary
-
Bookmarks:
- CiteULike: 1
- Citations:
- Appears in Collections:
Article: Increased expression of glycosyl-phosphatidylinositol anchor attachment protein 1 (GPAA1) is associated with gene amplification in hepatocellular carcinoma
Title | Increased expression of glycosyl-phosphatidylinositol anchor attachment protein 1 (GPAA1) is associated with gene amplification in hepatocellular carcinoma |
---|---|
Authors | |
Keywords | Differential expression GPI Tumorigenesis |
Issue Date | 2006 |
Publisher | John Wiley & Sons, Inc.. The Journal's web site is located at http://www3.interscience.wiley.com/journal/29331/home |
Citation | International Journal Of Cancer, 2006, v. 119 n. 6, p. 1330-1337 How to Cite? |
Abstract | Glycosyl-phosphatidylinositol (GPI) anchor attachment protein 1 (GPAA1) transcript level was frequently up-regulated in our earlier study on gene expression profile. We therefore analyzed the potential involvement of GPAA1 in hepatocellular carcinoma (HCC) as GPAA1 gene locates at chromosome 8q24.3 which chromosome region is frequently amplified in HCCs. In this study, we observed that GPAA1 transcript in the HCCs (n = 93) showed a significantly higher expression level compared with their paralleled adjacent nontumor liver tissues, cirrhosis (n = 15) and normal (n = 16) liver tissues using real-time quantitative RT-PCR (p < 0.005). We also demonstrated that GPAA1 protein up-regulation was common in HCCs (90%, 9/10), and GPAA1 gene was frequently amplified (73%, 11/15) using quantitative microsatellite analysis. Increased GPAA1 expression was significantly associated with HCCs poor cellular differentiation (p = 0.011) and poor prognosis (p = 0.010). We then modulated the GPAA1 expression level in HCC cells (Hep3B) by transfection experiments, which was shown to positively regulate cell adhesion ability (p = 0.004) and proliferation rate (p = 0.037). Our data revealed GPAA1 gene amplification with overexpression of RNA and protein in HCC. GPAA1 is a potential amplification target of chromosome 8q and responsible to regulate tumor cells behavior. © 2006 Wiley-Liss, Inc. |
Persistent Identifier | http://hdl.handle.net/10722/83576 |
ISSN | 2023 Impact Factor: 5.7 2023 SCImago Journal Rankings: 2.131 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Ho, JC | en_HK |
dc.contributor.author | Cheung, ST | en_HK |
dc.contributor.author | Patil, M | en_HK |
dc.contributor.author | Chen, X | en_HK |
dc.contributor.author | Fan, ST | en_HK |
dc.date.accessioned | 2010-09-06T08:42:40Z | - |
dc.date.available | 2010-09-06T08:42:40Z | - |
dc.date.issued | 2006 | en_HK |
dc.identifier.citation | International Journal Of Cancer, 2006, v. 119 n. 6, p. 1330-1337 | en_HK |
dc.identifier.issn | 0020-7136 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/83576 | - |
dc.description.abstract | Glycosyl-phosphatidylinositol (GPI) anchor attachment protein 1 (GPAA1) transcript level was frequently up-regulated in our earlier study on gene expression profile. We therefore analyzed the potential involvement of GPAA1 in hepatocellular carcinoma (HCC) as GPAA1 gene locates at chromosome 8q24.3 which chromosome region is frequently amplified in HCCs. In this study, we observed that GPAA1 transcript in the HCCs (n = 93) showed a significantly higher expression level compared with their paralleled adjacent nontumor liver tissues, cirrhosis (n = 15) and normal (n = 16) liver tissues using real-time quantitative RT-PCR (p < 0.005). We also demonstrated that GPAA1 protein up-regulation was common in HCCs (90%, 9/10), and GPAA1 gene was frequently amplified (73%, 11/15) using quantitative microsatellite analysis. Increased GPAA1 expression was significantly associated with HCCs poor cellular differentiation (p = 0.011) and poor prognosis (p = 0.010). We then modulated the GPAA1 expression level in HCC cells (Hep3B) by transfection experiments, which was shown to positively regulate cell adhesion ability (p = 0.004) and proliferation rate (p = 0.037). Our data revealed GPAA1 gene amplification with overexpression of RNA and protein in HCC. GPAA1 is a potential amplification target of chromosome 8q and responsible to regulate tumor cells behavior. © 2006 Wiley-Liss, Inc. | en_HK |
dc.language | eng | en_HK |
dc.publisher | John Wiley & Sons, Inc.. The Journal's web site is located at http://www3.interscience.wiley.com/journal/29331/home | en_HK |
dc.relation.ispartof | International Journal of Cancer | en_HK |
dc.rights | International Journal of Cancer. Copyright © John Wiley & Sons, Inc. | en_HK |
dc.subject | Differential expression | en_HK |
dc.subject | GPI | en_HK |
dc.subject | Tumorigenesis | en_HK |
dc.title | Increased expression of glycosyl-phosphatidylinositol anchor attachment protein 1 (GPAA1) is associated with gene amplification in hepatocellular carcinoma | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0020-7136&volume=119&issue=6&spage=1330&epage=1337&date=2006&atitle=Increased+expression+of+glycosyl-phosphatidylinositol+anchor+attachment+protein+1+(GPAA1)+is+associated+with+gene+amplification+in+hepatocellular+carcinoma | en_HK |
dc.identifier.email | Cheung, ST: stcheung@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 | Fan, ST=rp00355 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1002/ijc.22005 | en_HK |
dc.identifier.pmid | 16642471 | - |
dc.identifier.scopus | eid_2-s2.0-33747495216 | en_HK |
dc.identifier.hkuros | 119793 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-33747495216&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 119 | en_HK |
dc.identifier.issue | 6 | en_HK |
dc.identifier.spage | 1330 | en_HK |
dc.identifier.epage | 1337 | en_HK |
dc.identifier.isi | WOS:000239877200016 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Ho, JC=7402650173 | en_HK |
dc.identifier.scopusauthorid | Cheung, ST=7202473497 | en_HK |
dc.identifier.scopusauthorid | Patil, M=8559878100 | en_HK |
dc.identifier.scopusauthorid | Chen, X=8978110800 | en_HK |
dc.identifier.scopusauthorid | Fan, ST=7402678224 | en_HK |
dc.identifier.citeulike | 4235288 | - |
dc.identifier.issnl | 0020-7136 | - |