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Article: Epstein-Barr virus infection in immortalized nasopharyngeal epithelial cells: Regulation of infection and phenotypic characterization
Title | Epstein-Barr virus infection in immortalized nasopharyngeal epithelial cells: Regulation of infection and phenotypic characterization | ||||||
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Authors | |||||||
Keywords | Esptein-Barr virus Nasopharyngeal epithelial carcinoma Premalignant nasopharyngeal epithelium | ||||||
Issue Date | 2010 | ||||||
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, 2010, v. 127 n. 7, p. 1570-1583 How to Cite? | ||||||
Abstract | Epstein-Barr virus (EBV) infection has been postulated to be an early event involved in the pathogenesis of nasopharyngeal carcinomas (NPC). The lack of representative premalignant nasopharyngeal epithelial cell system for EBV infection has hampered research investigation into the regulation and involvement of EBV infection in NPC pathogenesis. We have compared the efficiency of EBV infection in nasopharyngeal epithelial cells with different biological properties including immortalized, primary and cancerous nasopharyngeal epithelial cells. EBV infection could be achieved in all the nasopharyngeal epithelial cells examined with variable infection rate. TGF-β effectively enhanced EBV infection into nasopharyngeal epithelial cells both in the immortalized and primary nasopharyngeal epithelial cells. Stable infection of EBV was achieved in a telomerase-immortalized nasopharyngeal epithelial cell line, NP460hTert. The expression pattern of EBV-encoded genes and biological properties of this EBV infected cell line on long-term propagation were monitored. The EBV-infected nasopharyngeal epithelial cells acquired anchorage-independent growth and exhibited invasive growth properties on prolonged propagation. A distinguished feature of this EBV-infected nasopharyngeal epithelial cell model was its enhanced ability to survive under growth factor and nutrient starvation. This was evidenced by the suppressed activation of apoptotic markers and sustained activation of pAkt of EBV-infected cells compared to control cells under nutrient starvation. Examination of cytokine profiles of EBV-infected NP460hTert cells to nutrient and growth factor deprivation revealed upregulation of expression of MCP-1 and GRO-α. The establishment of a stable EBV infection model of premalignant nasopharyngeal epithelial cells will facilitate research investigation into the pathogenic role of EBV in NPC development. © 2010 UICC. | ||||||
Persistent Identifier | http://hdl.handle.net/10722/149748 | ||||||
ISSN | 2023 Impact Factor: 5.7 2023 SCImago Journal Rankings: 2.131 | ||||||
ISI Accession Number ID |
Funding Information: Grant sponsor: University Grant Council, Hong Kong; Grant numbers: HKU 7770/07M, HKU 7766/08M; Grant sponsor: University of Hong Kong (CRCG grant) | ||||||
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Tsang, CM | en_HK |
dc.contributor.author | Zhang, G | en_HK |
dc.contributor.author | Seto, E | en_HK |
dc.contributor.author | Takada, K | en_HK |
dc.contributor.author | Deng, W | en_HK |
dc.contributor.author | Yip, YL | en_HK |
dc.contributor.author | Man, C | en_HK |
dc.contributor.author | Hau, PM | en_HK |
dc.contributor.author | Chen, H | en_HK |
dc.contributor.author | Cao, Y | en_HK |
dc.contributor.author | Lo, KW | en_HK |
dc.contributor.author | Middeldorp, JM | en_HK |
dc.contributor.author | Cheung, ALM | en_HK |
dc.contributor.author | Tsao, SW | en_HK |
dc.date.accessioned | 2012-06-26T05:57:57Z | - |
dc.date.available | 2012-06-26T05:57:57Z | - |
dc.date.issued | 2010 | en_HK |
dc.identifier.citation | International Journal Of Cancer, 2010, v. 127 n. 7, p. 1570-1583 | en_HK |
dc.identifier.issn | 0020-7136 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/149748 | - |
dc.description.abstract | Epstein-Barr virus (EBV) infection has been postulated to be an early event involved in the pathogenesis of nasopharyngeal carcinomas (NPC). The lack of representative premalignant nasopharyngeal epithelial cell system for EBV infection has hampered research investigation into the regulation and involvement of EBV infection in NPC pathogenesis. We have compared the efficiency of EBV infection in nasopharyngeal epithelial cells with different biological properties including immortalized, primary and cancerous nasopharyngeal epithelial cells. EBV infection could be achieved in all the nasopharyngeal epithelial cells examined with variable infection rate. TGF-β effectively enhanced EBV infection into nasopharyngeal epithelial cells both in the immortalized and primary nasopharyngeal epithelial cells. Stable infection of EBV was achieved in a telomerase-immortalized nasopharyngeal epithelial cell line, NP460hTert. The expression pattern of EBV-encoded genes and biological properties of this EBV infected cell line on long-term propagation were monitored. The EBV-infected nasopharyngeal epithelial cells acquired anchorage-independent growth and exhibited invasive growth properties on prolonged propagation. A distinguished feature of this EBV-infected nasopharyngeal epithelial cell model was its enhanced ability to survive under growth factor and nutrient starvation. This was evidenced by the suppressed activation of apoptotic markers and sustained activation of pAkt of EBV-infected cells compared to control cells under nutrient starvation. Examination of cytokine profiles of EBV-infected NP460hTert cells to nutrient and growth factor deprivation revealed upregulation of expression of MCP-1 and GRO-α. The establishment of a stable EBV infection model of premalignant nasopharyngeal epithelial cells will facilitate research investigation into the pathogenic role of EBV in NPC development. © 2010 UICC. | en_HK |
dc.language | eng | en_US |
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.subject | Esptein-Barr virus | en_HK |
dc.subject | Nasopharyngeal epithelial carcinoma | en_HK |
dc.subject | Premalignant nasopharyngeal epithelium | en_HK |
dc.title | Epstein-Barr virus infection in immortalized nasopharyngeal epithelial cells: Regulation of infection and phenotypic characterization | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Deng, W: wdeng@hkucc.hku.hk | en_HK |
dc.identifier.email | Chen, H: hlchen@hku.hk | en_HK |
dc.identifier.email | Cheung, ALM: lmcheung@hku.hk | en_HK |
dc.identifier.email | Tsao, SW: gswtsao@hku.hk | en_HK |
dc.identifier.authority | Deng, W=rp01640 | en_HK |
dc.identifier.authority | Chen, H=rp00383 | en_HK |
dc.identifier.authority | Cheung, ALM=rp00332 | en_HK |
dc.identifier.authority | Tsao, SW=rp00399 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1002/ijc.25173 | en_HK |
dc.identifier.scopus | eid_2-s2.0-77956601893 | en_HK |
dc.identifier.hkuros | 181771 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-77956601893&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 127 | en_HK |
dc.identifier.issue | 7 | en_HK |
dc.identifier.spage | 1570 | en_HK |
dc.identifier.epage | 1583 | en_HK |
dc.identifier.eissn | 1097-0215 | - |
dc.identifier.isi | WOS:000281340200008 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Tsang, CM=24831236400 | en_HK |
dc.identifier.scopusauthorid | Zhang, G=36544510100 | en_HK |
dc.identifier.scopusauthorid | Seto, E=8242003200 | en_HK |
dc.identifier.scopusauthorid | Takada, K=7403090730 | en_HK |
dc.identifier.scopusauthorid | Deng, W=7202223673 | en_HK |
dc.identifier.scopusauthorid | Yip, YL=7005596403 | en_HK |
dc.identifier.scopusauthorid | Man, C=7005722377 | en_HK |
dc.identifier.scopusauthorid | Hau, PM=14060079200 | en_HK |
dc.identifier.scopusauthorid | Chen, H=26643315400 | en_HK |
dc.identifier.scopusauthorid | Cao, Y=7404524499 | en_HK |
dc.identifier.scopusauthorid | Lo, KW=34872774800 | en_HK |
dc.identifier.scopusauthorid | Middeldorp, JM=35493462100 | en_HK |
dc.identifier.scopusauthorid | Cheung, ALM=7401806497 | en_HK |
dc.identifier.scopusauthorid | Tsao, SW=7102813116 | en_HK |
dc.identifier.issnl | 0020-7136 | - |