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- Publisher Website: 10.1016/j.jcv.2004.04.004
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- PMID: 15572001
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Article: Physical status of HPV-16 in esophageal squamous cell carcinoma
Title | Physical status of HPV-16 in esophageal squamous cell carcinoma |
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Authors | |
Keywords | ESCC Esophageal cancer esophageal squamous cell carcinoma Esophageal squamous cell carcinoma HPV human papillomavirus Human papillomavirus Integration opening reading frame ORF PCR Physical status polymerase chain reaction |
Issue Date | 2005 |
Publisher | Elsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/jcv |
Citation | Journal Of Clinical Virology, 2005, v. 32 n. 1, p. 19-23 How to Cite? |
Abstract | Background: Infection with high-risk human papillomavirus (HPV) has been implicated as one of the risk factors of esophageal squamous cell carcinoma (ESCC). Integration of viral DNA into host genome is essential for carcinogenesis since it promotes disruption of the HPV E2 gene, leading to abnormal expression of E6 and E7 oncoproteins. Objectives and study design: To investigate the viral integration status of HPV-16 infection in ESCC, 35 HPV-positive ESCC specimens collected from Chinese patients were subject to real-time quantitative PCR for determination of physical status of HPV-16 by analyzing the ratios of E2 to E6 genes. Results: Our results showed that only 8.6% (3/35) of the HPV-16 positive specimens harbored exclusively the episomal form (i.e. E2/E6 ratio ≥ 1), whereas the remaining 91.4% contained either only the integrated form (5.7%, with E2/E6 ratio = 0) or a mixture of episomal and integrated forms of viral molecules (85.7%, with E2/E6 ratios > 0 but <1). Amongst the 30 cancer specimens carrying mixed integrated and episomal forms, 28 had E2/integrated E6 ratios of less than 1, indicating a predominance of integrated form of viral genes in these lesions. Conclusion: Our finding of frequent integration of viral DNA in the host genome suggests that integration HPV-16 is common in ESCC from Chinese patients and implies that HPV infection may play a role in the pathogenesis of ESCC. © 2004 Elsevier B.V. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/67724 |
ISSN | 2023 Impact Factor: 4.0 2023 SCImago Journal Rankings: 1.344 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Si, HX | en_HK |
dc.contributor.author | Tsao, SW | en_HK |
dc.contributor.author | Poon, CSP | en_HK |
dc.contributor.author | Wong, YC | en_HK |
dc.contributor.author | Cheung, ALM | en_HK |
dc.date.accessioned | 2010-09-06T05:57:41Z | - |
dc.date.available | 2010-09-06T05:57:41Z | - |
dc.date.issued | 2005 | en_HK |
dc.identifier.citation | Journal Of Clinical Virology, 2005, v. 32 n. 1, p. 19-23 | en_HK |
dc.identifier.issn | 1386-6532 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/67724 | - |
dc.description.abstract | Background: Infection with high-risk human papillomavirus (HPV) has been implicated as one of the risk factors of esophageal squamous cell carcinoma (ESCC). Integration of viral DNA into host genome is essential for carcinogenesis since it promotes disruption of the HPV E2 gene, leading to abnormal expression of E6 and E7 oncoproteins. Objectives and study design: To investigate the viral integration status of HPV-16 infection in ESCC, 35 HPV-positive ESCC specimens collected from Chinese patients were subject to real-time quantitative PCR for determination of physical status of HPV-16 by analyzing the ratios of E2 to E6 genes. Results: Our results showed that only 8.6% (3/35) of the HPV-16 positive specimens harbored exclusively the episomal form (i.e. E2/E6 ratio ≥ 1), whereas the remaining 91.4% contained either only the integrated form (5.7%, with E2/E6 ratio = 0) or a mixture of episomal and integrated forms of viral molecules (85.7%, with E2/E6 ratios > 0 but <1). Amongst the 30 cancer specimens carrying mixed integrated and episomal forms, 28 had E2/integrated E6 ratios of less than 1, indicating a predominance of integrated form of viral genes in these lesions. Conclusion: Our finding of frequent integration of viral DNA in the host genome suggests that integration HPV-16 is common in ESCC from Chinese patients and implies that HPV infection may play a role in the pathogenesis of ESCC. © 2004 Elsevier B.V. All rights reserved. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Elsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/jcv | en_HK |
dc.relation.ispartof | Journal of Clinical Virology | en_HK |
dc.rights | Journal of Clinical Virology. Copyright © Elsevier BV. | en_HK |
dc.subject | ESCC | - |
dc.subject | Esophageal cancer | - |
dc.subject | esophageal squamous cell carcinoma | - |
dc.subject | Esophageal squamous cell carcinoma | - |
dc.subject | HPV | - |
dc.subject | human papillomavirus | - |
dc.subject | Human papillomavirus | - |
dc.subject | Integration | - |
dc.subject | opening reading frame | - |
dc.subject | ORF | - |
dc.subject | PCR | - |
dc.subject | Physical status | - |
dc.subject | polymerase chain reaction | - |
dc.subject.mesh | Carcinoma, Squamous Cell - genetics - pathology - virology | en_HK |
dc.subject.mesh | DNA-Binding Proteins - genetics | en_HK |
dc.subject.mesh | Esophageal Neoplasms - genetics - pathology - virology | en_HK |
dc.subject.mesh | Humans | en_HK |
dc.subject.mesh | Oncogene Proteins, Viral - genetics | en_HK |
dc.subject.mesh | Papillomaviridae - classification - genetics - isolation & purification | en_HK |
dc.subject.mesh | Papillomavirus Infections - complications | en_HK |
dc.subject.mesh | Repressor Proteins - genetics | en_HK |
dc.subject.mesh | Virus Integration - genetics | en_HK |
dc.title | Physical status of HPV-16 in esophageal squamous cell carcinoma | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1386-6532&volume=32&spage=19&epage=23&date=2005&atitle=Physical+status+of+HPV-16+in+esophageal+squamous+cell+carcinoma | en_HK |
dc.identifier.email | Tsao, SW:gswtsao@hkucc.hku.hk | en_HK |
dc.identifier.email | Wong, YC:ycwong@hkucc.hku.hk | en_HK |
dc.identifier.email | Cheung, ALM:lmcheung@hkucc.hku.hk | en_HK |
dc.identifier.authority | Tsao, SW=rp00399 | en_HK |
dc.identifier.authority | Wong, YC=rp00316 | en_HK |
dc.identifier.authority | Cheung, ALM=rp00332 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.jcv.2004.04.004 | en_HK |
dc.identifier.pmid | 15572001 | - |
dc.identifier.scopus | eid_2-s2.0-9644258597 | en_HK |
dc.identifier.hkuros | 96582 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-9644258597&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 32 | en_HK |
dc.identifier.issue | 1 | en_HK |
dc.identifier.spage | 19 | en_HK |
dc.identifier.epage | 23 | en_HK |
dc.identifier.isi | WOS:000226189600003 | - |
dc.publisher.place | Netherlands | en_HK |
dc.identifier.scopusauthorid | Si, HX=36780537100 | en_HK |
dc.identifier.scopusauthorid | Tsao, SW=7102813116 | en_HK |
dc.identifier.scopusauthorid | Poon, CSP=7202672697 | en_HK |
dc.identifier.scopusauthorid | Wong, YC=7403041798 | en_HK |
dc.identifier.scopusauthorid | Cheung, ALM=7401806497 | en_HK |
dc.identifier.issnl | 1386-6532 | - |