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Article: Detection of Epstein-Barr virus (EBV)-encoded microRNAs in plasma of patients with nasopharyngeal carcinoma

TitleDetection of Epstein-Barr virus (EBV)-encoded microRNAs in plasma of patients with nasopharyngeal carcinoma
Authors
Keywordscirculating nucleic acid
EBV DNA
EBV‐encoded microRNA
Epstein–Barr virus
nasopharyngeal carcinoma
Issue Date2019
PublisherJohn Wiley & Sons, Inc. The Journal's web site is located at http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-0347
Citation
Head & Neck, 2019, v. 41 n. 3, p. 780-792 How to Cite?
AbstractBackground: Nasopharyngeal carcinoma (NPC) latently infected by Epstein–Barr virus (EBV) expresses 40 EBV BART microRNAs (miRNAs). Difference in diagnostic efficacy of these miRNAs on NPC detection was observed. Here, we performed a comprehensive evaluation on the efficacy of these miRNAs. Methods: Quantitative polymerase chain reaction was performed on plasma nucleic acid isolated from patients with NPC and noncancer donors. Results: For primary NPC, BART2‐5P, BART6‐3P, BART7‐3P, BART7‐5P, BART9‐5P, BART11‐3P, BART17‐5P, and BART19‐5P were significantly elevated. For recurrent NPC, plasma levels of BART2‐3P, BART2‐5P, BART5‐3P, BART5‐5P, BART6‐3P, BART8‐3P, BART9‐5P, BART17‐5P, BART19‐3P, and BART20‐3P were significantly increased. Area under curve (AUC) analysis showed that BART19‐5P had the best performance to identify NPC which was serologically EBV DNA undetectable. For recurrent NPC, BART8‐3P and BART10‐3P had highest AUC value for identifying cancer in EBV DNA undetectable plasma. Conclusion: Our data supported the use of circulating EBV miRNAs in NPC and recurrent NPC detection.
Persistent Identifierhttp://hdl.handle.net/10722/272983
ISSN
2021 Impact Factor: 3.821
2020 SCImago Journal Rankings: 1.012
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorGao, W-
dc.contributor.authorWong, TS-
dc.contributor.authorLv, KX-
dc.contributor.authorZhang, MJ-
dc.contributor.authorTsang, RKY-
dc.contributor.authorChan, JYW-
dc.date.accessioned2019-08-06T09:20:23Z-
dc.date.available2019-08-06T09:20:23Z-
dc.date.issued2019-
dc.identifier.citationHead & Neck, 2019, v. 41 n. 3, p. 780-792-
dc.identifier.issn1043-3074-
dc.identifier.urihttp://hdl.handle.net/10722/272983-
dc.description.abstractBackground: Nasopharyngeal carcinoma (NPC) latently infected by Epstein–Barr virus (EBV) expresses 40 EBV BART microRNAs (miRNAs). Difference in diagnostic efficacy of these miRNAs on NPC detection was observed. Here, we performed a comprehensive evaluation on the efficacy of these miRNAs. Methods: Quantitative polymerase chain reaction was performed on plasma nucleic acid isolated from patients with NPC and noncancer donors. Results: For primary NPC, BART2‐5P, BART6‐3P, BART7‐3P, BART7‐5P, BART9‐5P, BART11‐3P, BART17‐5P, and BART19‐5P were significantly elevated. For recurrent NPC, plasma levels of BART2‐3P, BART2‐5P, BART5‐3P, BART5‐5P, BART6‐3P, BART8‐3P, BART9‐5P, BART17‐5P, BART19‐3P, and BART20‐3P were significantly increased. Area under curve (AUC) analysis showed that BART19‐5P had the best performance to identify NPC which was serologically EBV DNA undetectable. For recurrent NPC, BART8‐3P and BART10‐3P had highest AUC value for identifying cancer in EBV DNA undetectable plasma. Conclusion: Our data supported the use of circulating EBV miRNAs in NPC and recurrent NPC detection.-
dc.languageeng-
dc.publisherJohn Wiley & Sons, Inc. The Journal's web site is located at http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-0347-
dc.relation.ispartofHead & Neck-
dc.rightsThis is the peer reviewed version of the following article: [FULL CITE], which has been published in final form at [Link to final article using the DOI]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.-
dc.subjectcirculating nucleic acid-
dc.subjectEBV DNA-
dc.subjectEBV‐encoded microRNA-
dc.subjectEpstein–Barr virus-
dc.subjectnasopharyngeal carcinoma-
dc.titleDetection of Epstein-Barr virus (EBV)-encoded microRNAs in plasma of patients with nasopharyngeal carcinoma-
dc.typeArticle-
dc.identifier.emailGao, W: weigaoi@hku.hk-
dc.identifier.emailWong, TS: wongtsa@hkucc.hku.hk-
dc.identifier.emailTsang, RKY: rkytsang@hku.hk-
dc.identifier.emailChan, JYW: jywchan1@HKUCC-COM.hku.hk-
dc.identifier.authorityGao, W=rp02222-
dc.identifier.authorityWong, TS=rp00478-
dc.identifier.authorityTsang, RKY=rp01386-
dc.identifier.authorityChan, JYW=rp01314-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1002/hed.25544-
dc.identifier.pmid30548946-
dc.identifier.scopuseid_2-s2.0-85058396457-
dc.identifier.hkuros299864-
dc.identifier.volume41-
dc.identifier.issue3-
dc.identifier.spage780-
dc.identifier.epage792-
dc.identifier.isiWOS:000459219300030-
dc.publisher.placeUnited States-
dc.identifier.issnl1043-3074-

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