File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1038/sj.onc.1209001
- Scopus: eid_2-s2.0-30544454169
- PMID: 16116475
- WOS: WOS:000234583600016
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Identification of RASSF1A modulated genes in nasopharyngeal carcinoma
Title | Identification of RASSF1A modulated genes in nasopharyngeal carcinoma |
---|---|
Authors | |
Keywords | Id2 Microarray Nasopharyngeal carcinoma RASSF1A Tumor suppressor |
Issue Date | 2006 |
Publisher | Nature Publishing Group. The Journal's web site is located at http://www.nature.com/onc |
Citation | Oncogene, 2006, v. 25 n. 2, p. 310-316 How to Cite? |
Abstract | RASSF1A is a tumor suppressor gene on 3p21.3 frequently inactivated by promoter hypermethylation in nasopharyngeal carcinoma (NPC). To identify RASSF1A target genes in NPC, we have investigated the expression profile of the stable RASSF1A transfectants and controls by high-density oligonucleotide array. A total of 57 genes showed differential expression in the RASSF1A-expressing cells. These RASSF1A target genes were involved in multiple cellular regulatory processes such as transcription, signal transduction, cell adhesion and RNA processing. The RASSF1A-modulated expression of eight selected genes with the highest fold changes (ATF5, TCRB, RGS1, activin βE, HNRPH1, HNRPD, Id2 and CKS2) by RASSF1A was confirmed in both stable and transient transfectants. Compared with the RASSF1A transfectants, an inverse expression pattern of activin βE, Id2 and ATF5 was shown in the immortalized nasopharyngeal epithelial cells treated with siRNA against RASSF1A. The findings imply that the expression of activin βE, Id2 and ATF5 was tightly regulated by RASSF1A and may associate with its tumor suppressor function. Strikingly, overexpression of Id2 is common in NPC and RASSF1A-induced repression of Id2 was mediated by the overexpression of activin βE. The results suggest a novel RASSF1A pathway in which both activin βE and Id2 are involved. © 2006 Nature Publishing Group All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/67899 |
ISSN | 2023 Impact Factor: 6.9 2023 SCImago Journal Rankings: 2.334 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Chow, LSN | en_HK |
dc.contributor.author | Lam, CW | en_HK |
dc.contributor.author | Chan, SYY | en_HK |
dc.contributor.author | Tsao, SW | en_HK |
dc.contributor.author | To, KF | en_HK |
dc.contributor.author | Tong, SF | en_HK |
dc.contributor.author | Hung, WK | en_HK |
dc.contributor.author | Dammann, R | en_HK |
dc.contributor.author | Huang, DP | en_HK |
dc.contributor.author | Lo, KW | en_HK |
dc.date.accessioned | 2010-09-06T05:59:17Z | - |
dc.date.available | 2010-09-06T05:59:17Z | - |
dc.date.issued | 2006 | en_HK |
dc.identifier.citation | Oncogene, 2006, v. 25 n. 2, p. 310-316 | en_HK |
dc.identifier.issn | 0950-9232 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/67899 | - |
dc.description.abstract | RASSF1A is a tumor suppressor gene on 3p21.3 frequently inactivated by promoter hypermethylation in nasopharyngeal carcinoma (NPC). To identify RASSF1A target genes in NPC, we have investigated the expression profile of the stable RASSF1A transfectants and controls by high-density oligonucleotide array. A total of 57 genes showed differential expression in the RASSF1A-expressing cells. These RASSF1A target genes were involved in multiple cellular regulatory processes such as transcription, signal transduction, cell adhesion and RNA processing. The RASSF1A-modulated expression of eight selected genes with the highest fold changes (ATF5, TCRB, RGS1, activin βE, HNRPH1, HNRPD, Id2 and CKS2) by RASSF1A was confirmed in both stable and transient transfectants. Compared with the RASSF1A transfectants, an inverse expression pattern of activin βE, Id2 and ATF5 was shown in the immortalized nasopharyngeal epithelial cells treated with siRNA against RASSF1A. The findings imply that the expression of activin βE, Id2 and ATF5 was tightly regulated by RASSF1A and may associate with its tumor suppressor function. Strikingly, overexpression of Id2 is common in NPC and RASSF1A-induced repression of Id2 was mediated by the overexpression of activin βE. The results suggest a novel RASSF1A pathway in which both activin βE and Id2 are involved. © 2006 Nature Publishing Group All rights reserved. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Nature Publishing Group. The Journal's web site is located at http://www.nature.com/onc | en_HK |
dc.relation.ispartof | Oncogene | en_HK |
dc.subject | Id2 | en_HK |
dc.subject | Microarray | en_HK |
dc.subject | Nasopharyngeal carcinoma | en_HK |
dc.subject | RASSF1A | en_HK |
dc.subject | Tumor suppressor | en_HK |
dc.subject.mesh | Gene Expression Profiling | en_HK |
dc.subject.mesh | Gene Expression Regulation, Neoplastic | en_HK |
dc.subject.mesh | Gene Silencing | en_HK |
dc.subject.mesh | Humans | en_HK |
dc.subject.mesh | Inhibin-beta Subunits - genetics - metabolism | en_HK |
dc.subject.mesh | Inhibitor of Differentiation Protein 2 - genetics - metabolism | en_HK |
dc.subject.mesh | Nasopharyngeal Neoplasms - genetics - metabolism | en_HK |
dc.subject.mesh | Oligonucleotide Array Sequence Analysis | en_HK |
dc.subject.mesh | Reverse Transcriptase Polymerase Chain Reaction | en_HK |
dc.subject.mesh | Signal Transduction | en_HK |
dc.subject.mesh | Transfection | en_HK |
dc.subject.mesh | Tumor Cells, Cultured | en_HK |
dc.subject.mesh | Tumor Markers, Biological - genetics - metabolism | en_HK |
dc.subject.mesh | Tumor Suppressor Proteins - antagonists & inhibitors - genetics - metabolism | en_HK |
dc.title | Identification of RASSF1A modulated genes in nasopharyngeal carcinoma | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0950-9232&volume=&spage=310&epage=316&date=2005&atitle=Identification+of+RASSF1A+modulated+genes+in+nasopharyngeal+carcinoma | en_HK |
dc.identifier.email | Lam, CW:ching-wanlam@pathology.hku.hk | en_HK |
dc.identifier.email | Tsao, SW:gswtsao@hkucc.hku.hk | en_HK |
dc.identifier.authority | Lam, CW=rp00260 | en_HK |
dc.identifier.authority | Tsao, SW=rp00399 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1038/sj.onc.1209001 | en_HK |
dc.identifier.pmid | 16116475 | - |
dc.identifier.scopus | eid_2-s2.0-30544454169 | en_HK |
dc.identifier.hkuros | 109869 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-30544454169&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 25 | en_HK |
dc.identifier.issue | 2 | en_HK |
dc.identifier.spage | 310 | en_HK |
dc.identifier.epage | 316 | en_HK |
dc.identifier.isi | WOS:000234583600016 | - |
dc.publisher.place | United Kingdom | en_HK |
dc.identifier.scopusauthorid | Chow, LSN=7202533094 | en_HK |
dc.identifier.scopusauthorid | Lam, CW=34570692600 | en_HK |
dc.identifier.scopusauthorid | Chan, SYY=34973871600 | en_HK |
dc.identifier.scopusauthorid | Tsao, SW=7102813116 | en_HK |
dc.identifier.scopusauthorid | To, KF=7101911940 | en_HK |
dc.identifier.scopusauthorid | Tong, SF=7201486672 | en_HK |
dc.identifier.scopusauthorid | Hung, WK=13310033500 | en_HK |
dc.identifier.scopusauthorid | Dammann, R=6701505261 | en_HK |
dc.identifier.scopusauthorid | Huang, DP=7403891486 | en_HK |
dc.identifier.scopusauthorid | Lo, KW=34872774800 | en_HK |
dc.identifier.citeulike | 307412 | - |
dc.identifier.issnl | 0950-9232 | - |