Epstein-Barr Virus-Based Nasopharyngeal Carcinoma (NPC) Risk Prediction Scores Are Elevated in NPC Multiplex Family Members in Taiwan
Abstract Nasopharyngeal carcinoma (NPC) is caused by Epstein-Barr virus (EBV) and is more likely to occur in susceptible families. Whether genetic susceptibility operates through altered EBV control is incompletely understood. We used a NPC risk prediction model based on 14 EBV markers to compare ri...
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Published in | The Journal of infectious diseases Vol. 223; no. 3; pp. 441 - 444 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Oxford University Press
13.02.2021
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ISSN | 0022-1899 1537-6613 1537-6613 |
DOI | 10.1093/infdis/jiaa385 |
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Abstract | Abstract
Nasopharyngeal carcinoma (NPC) is caused by Epstein-Barr virus (EBV) and is more likely to occur in susceptible families. Whether genetic susceptibility operates through altered EBV control is incompletely understood. We used a NPC risk prediction model based on 14 EBV markers to compare risk score distribution in unaffected members from multiplex families with that in population-based controls. Despite the absence of NPC at the time of antibody measurement, we observed an upward shift in risk score among multiplex family members compared to the general population, consistent with the possibility that genetic factors affect NPC risk through alterations in EBV control. |
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AbstractList | Nasopharyngeal carcinoma (NPC) is caused by Epstein-Barr virus (EBV) and is more likely to occur in susceptible families. Whether genetic susceptibility operates through altered EBV control is incompletely understood. We used a NPC risk prediction model based on 14 EBV markers to compare risk score distribution in unaffected members from multiplex families with that in population-based controls. Despite the absence of NPC at the time of antibody measurement, we observed an upward shift in risk score among multiplex family members compared to the general population, consistent with the possibility that genetic factors affect NPC risk through alterations in EBV control. Abstract Nasopharyngeal carcinoma (NPC) is caused by Epstein-Barr virus (EBV) and is more likely to occur in susceptible families. Whether genetic susceptibility operates through altered EBV control is incompletely understood. We used a NPC risk prediction model based on 14 EBV markers to compare risk score distribution in unaffected members from multiplex families with that in population-based controls. Despite the absence of NPC at the time of antibody measurement, we observed an upward shift in risk score among multiplex family members compared to the general population, consistent with the possibility that genetic factors affect NPC risk through alterations in EBV control. Nasopharyngeal carcinoma (NPC) is caused by Epstein-Barr virus (EBV) and is more likely to occur in susceptible families. Whether genetic susceptibility operates through altered EBV control is incompletely understood. We used a NPC risk prediction model based on 14 EBV markers to compare risk score distribution in unaffected members from multiplex families with that in population-based controls. Despite the absence of NPC at the time of antibody measurement, we observed an upward shift in risk score among multiplex family members compared to the general population, consistent with the possibility that genetic factors affect NPC risk through alterations in EBV control.Nasopharyngeal carcinoma (NPC) is caused by Epstein-Barr virus (EBV) and is more likely to occur in susceptible families. Whether genetic susceptibility operates through altered EBV control is incompletely understood. We used a NPC risk prediction model based on 14 EBV markers to compare risk score distribution in unaffected members from multiplex families with that in population-based controls. Despite the absence of NPC at the time of antibody measurement, we observed an upward shift in risk score among multiplex family members compared to the general population, consistent with the possibility that genetic factors affect NPC risk through alterations in EBV control. |
Author | Chien, Yin-Chu Yu, Kelly J Lee, Mei-Hsuan Hildesheim, Allan Wang, Cheng-Ping Liu, Zhiwei Chen, Chien-Jen Hsu, Wan-Lun Coghill, Anna E Chen, Tseng-Cheng Huang, Yu-Han |
AuthorAffiliation | 1 Institute of Clinical Medicine, National Yang-Ming University , Taipei, Taiwan 2 Cancer Epidemiology Program, Division of Population Science, H. Lee Moffitt Cancer Center and Research Institute , Tampa, Florida, USA 5 Genomics Research Center, Academia Sinica , Taipei, Taiwan 6 Department of Otolaryngology, National Taiwan University Hospital and College of Medicine , Taipei, Taiwan 4 Graduate Institute of Epidemiology and Preventive Medicine, College of Public Health, National Taiwan University , Taipei, Taiwan 3 Infections and Immunoepidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute , Bethesda, Maryland, USA |
AuthorAffiliation_xml | – name: 1 Institute of Clinical Medicine, National Yang-Ming University , Taipei, Taiwan – name: 6 Department of Otolaryngology, National Taiwan University Hospital and College of Medicine , Taipei, Taiwan – name: 2 Cancer Epidemiology Program, Division of Population Science, H. Lee Moffitt Cancer Center and Research Institute , Tampa, Florida, USA – name: 3 Infections and Immunoepidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute , Bethesda, Maryland, USA – name: 4 Graduate Institute of Epidemiology and Preventive Medicine, College of Public Health, National Taiwan University , Taipei, Taiwan – name: 5 Genomics Research Center, Academia Sinica , Taipei, Taiwan |
Author_xml | – sequence: 1 givenname: Mei-Hsuan surname: Lee fullname: Lee, Mei-Hsuan email: meihlee@ntu.edu.tw organization: Institute of Clinical Medicine, National Yang-Ming University, Taipei, Taiwan – sequence: 2 givenname: Yu-Han surname: Huang fullname: Huang, Yu-Han organization: Institute of Clinical Medicine, National Yang-Ming University, Taipei, Taiwan – sequence: 3 givenname: Anna E surname: Coghill fullname: Coghill, Anna E organization: Cancer Epidemiology Program, Division of Population Science, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA – sequence: 4 givenname: Zhiwei orcidid: 0000-0002-0136-651X surname: Liu fullname: Liu, Zhiwei organization: Infections and Immunoepidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland, USA – sequence: 5 givenname: Kelly J surname: Yu fullname: Yu, Kelly J organization: Infections and Immunoepidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland, USA – sequence: 6 givenname: Wan-Lun surname: Hsu fullname: Hsu, Wan-Lun organization: Graduate Institute of Epidemiology and Preventive Medicine, College of Public Health, National Taiwan University, Taipei, Taiwan – sequence: 7 givenname: Yin-Chu surname: Chien fullname: Chien, Yin-Chu organization: Genomics Research Center, Academia Sinica, Taipei, Taiwan – sequence: 8 givenname: Cheng-Ping surname: Wang fullname: Wang, Cheng-Ping organization: Department of Otolaryngology, National Taiwan University Hospital and College of Medicine, Taipei, Taiwan – sequence: 9 givenname: Tseng-Cheng surname: Chen fullname: Chen, Tseng-Cheng organization: Department of Otolaryngology, National Taiwan University Hospital and College of Medicine, Taipei, Taiwan – sequence: 10 givenname: Chien-Jen surname: Chen fullname: Chen, Chien-Jen organization: Genomics Research Center, Academia Sinica, Taipei, Taiwan – sequence: 11 givenname: Allan orcidid: 0000-0003-0257-2363 surname: Hildesheim fullname: Hildesheim, Allan organization: Infections and Immunoepidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland, USA |
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Keywords | host-virus interactions immune genetic susceptibility virus control multiplex antibody array |
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References | Hildesheim (2021032204350864200_CIT0014) 2002; 94 Chen (2021032204350864200_CIT0013) 2006; 295 Ji (2021032204350864200_CIT0003) 2019; 30 Yu (2021032204350864200_CIT0011) 2011; 17 Yu (2021032204350864200_CIT0008) 2019; 9 Coghill (2021032204350864200_CIT0010) 2018; 99 Liu (2021032204350864200_CIT0002) 2013; 177 Yu (2021032204350864200_CIT0006) 2009; 124 Hildesheim (2021032204350864200_CIT0004) 2013; 177 Rubicz (2021032204350864200_CIT0015) 2013; 9 Hildesheim (2021032204350864200_CIT0007) 2012; 22 Chang (2021032204350864200_CIT0001) 2006; 15 Coghill (2021032204350864200_CIT0005) 2018; 24 Pickard (2021032204350864200_CIT0009) 2004; 111 Guo (2021032204350864200_CIT0012) 2009; 124 |
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Nasopharyngeal carcinoma (NPC) is caused by Epstein-Barr virus (EBV) and is more likely to occur in susceptible families. Whether genetic... Nasopharyngeal carcinoma (NPC) is caused by Epstein-Barr virus (EBV) and is more likely to occur in susceptible families. Whether genetic susceptibility... |
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SubjectTerms | Epstein-Barr virus Families & family life Genetic factors Head & neck cancer Health risks Major and Brief Reports Nasopharyngeal carcinoma Prediction models Throat cancer |
Title | Epstein-Barr Virus-Based Nasopharyngeal Carcinoma (NPC) Risk Prediction Scores Are Elevated in NPC Multiplex Family Members in Taiwan |
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