Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer.

Corina Lesseur; Brenda Diergaarde; Andrew F. Olshan; Victor Wünsch-Filho; Andrew R. Ness; Geoffrey Liu; Martin Lacko; José Eluf-Neto; Silvia Franceschi; Pagona Lagiou; Gary J. Macfarlane; Lorenzo Richiardi; Stefania Boccia; Jerry Polesel; Kristina Kjaerheim; David Zaridze; Mattias Johansson; Ana M. Menezes; Maria Paula Curado; Max Robinson; Wolfgang Ahrens; Cristina Canova; Ariana Znaor; Xavier Castellsagué; David I. Conway; Ivana Holcátová; Dana Mates; Marta Vilensky; Claire M Healy; Neonila Szeszenia-Dabrowska; Eleonóra Fabiánová; Jolanta Lissowska; Jennifer R. Grandis; Mark C. Weissler; Eloiza H. Tajara; Fabio D. Nunes; Marcos B. De Carvalho; Steve Thomas; Rayjean J. Hung; Wilbert H.M. Peters; Rolando Herrero; Gabriella Cadoni; H. Bas Bueno-De-Mesquita; Annika Steffen; Antonio Agudo; Oxana Shangina; Xiangjun Xiao; Valérie Gaborieau; Amélie Chabrier; Devasena Anantharaman; Paolo Boffetta; Christopher I. Amos; James D. Mckay; Paul Brennan

doi:10.1038/ng.3685

Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer.

Corina Lesseur
, Brenda Diergaarde
, Andrew F. Olshan
, Victor Wünsch-Filho
, Andrew R. Ness
, Geoffrey Liu^*
, Martin Lacko
, José Eluf-Neto
, Silvia Franceschi
, Pagona Lagiou
, Gary J. Macfarlane
, Lorenzo Richiardi
, Stefania Boccia
, Jerry Polesel
, Kristina Kjaerheim
, David Zaridze
, Mattias Johansson
, Ana M. Menezes
, Maria Paula Curado
, Max Robinson

Wolfgang Ahrens, Cristina Canova, Ariana Znaor, Xavier Castellsagué, David I. Conway, Ivana Holcátová, Dana Mates, Marta Vilensky, Claire M Healy, Neonila Szeszenia-Dabrowska, Eleonóra Fabiánová, Jolanta Lissowska, Jennifer R. Grandis, Mark C. Weissler, Eloiza H. Tajara, Fabio D. Nunes, Marcos B. De Carvalho, Steve Thomas, Rayjean J. Hung, Wilbert H.M. Peters, Rolando Herrero, Gabriella Cadoni, H. Bas Bueno-De-Mesquita, Annika Steffen, Antonio Agudo, Oxana Shangina, Xiangjun Xiao, Valérie Gaborieau, Amélie Chabrier, Devasena Anantharaman, Paolo Boffetta, Christopher I. Amos, James D. Mckay, Paul Brennan

^*Autore corrispondente per questo lavoro

International Agency for Research on Cancer
University of Pittsburgh
University of North Carolina at Chapel Hill
Universidade de São Paulo
Health Protection Research Unit in Healthcare Associated Infections and Antimicrobial Resistance
Princess Margaret Cancer Centre
Maastricht University
National and Kapodistrian University of Athens
University of Aberdeen
University of Turin
IRCCS Centro di Riferimento Oncologico - Aviano PN
Cancer Registry of Norway Institute of Population-Based Cancer Research
Russian Ministry of Health
Universidade Federal de Pelotas
A.C.Camargo Cancer Center
Newcastle University
Leibniz Institute for Prevention Research and Epidemiology
University of Padua
Bellvitge Biomedical Research Institute
University of Glasgow
Charles University
Institutul de Sanatate Publica
Universidad de Buenos Aires
Trinity College Dublin
Nofer Institute of Occupational Medicine
Regional Authority of Public Health
Maria Sklodowska-Curie Institute of Oncology
University of California at San Francisco
School of Medicine of São José do Rio Preto
Heliopolis Hospital
University of Bristol
Mount Sinai Hospital
Radboud University Nijmegen
National Institute of Public Health and the Environment
German Institute of Human Nutrition Potsdam-Rehbruecke
Dartmouth College

Risultato della ricerca: Contributo in rivista › Articolo › peer review

73 Citazioni (Scopus)

Abstract

We conducted a genome-wide association study of oral cavity and pharyngeal cancer in 6,034 cases and 6,585 controls from Europe, North America and South America. We detected eight significantly associated loci (P < 5 × 10−8), seven of which are new for these cancer sites. Oral and pharyngeal cancers combined were associated with loci at 6p21.32 (rs3828805, HLA-DQB1), 10q26.13 (rs201982221, LHPP) and 11p15.4 (rs1453414, OR52N2–TRIM5). Oral cancer was associated with two new regions, 2p23.3 (rs6547741, GPN1) and 9q34.12 (rs928674, LAMC3), and with known cancer-related loci—9p21.3 (rs8181047, CDKN2B-AS1) and 5p15.33 (rs10462706, CLPTM1L). Oropharyngeal cancer associations were limited to the human leukocyte antigen (HLA) region, and classical HLA allele imputation showed a protective association with the class II haplotype HLA-DRB1*1301–HLA-DQA1*0103–HLA-DQB1*0603 (odds ratio (OR) = 0.59, P = 2.7 × 10−9). Stratified analyses on a subgroup of oropharyngeal cases with information available on human papillomavirus (HPV) status indicated that this association was considerably stronger in HPV-positive (OR = 0.23, P = 1.6 × 10−6) than in HPV-negative (OR = 0.75, P = 0.16) cancers.

Lingua originale	Inglese
pagine (da-a)	1544-1550
Numero di pagine	7
Rivista	Nature Genetics
Volume	2016
DOI	https://doi.org/10.1038/ng.3685
Stato di pubblicazione	Pubblicato - 2016

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Keywords

oral cancer

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10.1038/ng.3685

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Lesseur, C., Diergaarde, B., Olshan, A. F., Wünsch-Filho, V., Ness, A. R., Liu, G., Lacko, M., Eluf-Neto, J., Franceschi, S., Lagiou, P., Macfarlane, G. J., Richiardi, L., Boccia, S., Polesel, J., Kjaerheim, K., Zaridze, D., Johansson, M., Menezes, A. M., Curado, M. P., ... Brennan, P. (2016). Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer. Nature Genetics, 2016, 1544-1550. https://doi.org/10.1038/ng.3685

@article{51c11f19370f42979249ff38cb2c0f48,

title = "Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer.",

abstract = "We conducted a genome-wide association study of oral cavity and pharyngeal cancer in 6,034 cases and 6,585 controls from Europe, North America and South America. We detected eight significantly associated loci (P < 5 {\texttimes} 10−8), seven of which are new for these cancer sites. Oral and pharyngeal cancers combined were associated with loci at 6p21.32 (rs3828805, HLA-DQB1), 10q26.13 (rs201982221, LHPP) and 11p15.4 (rs1453414, OR52N2{\textendash}TRIM5). Oral cancer was associated with two new regions, 2p23.3 (rs6547741, GPN1) and 9q34.12 (rs928674, LAMC3), and with known cancer-related loci{\textemdash}9p21.3 (rs8181047, CDKN2B-AS1) and 5p15.33 (rs10462706, CLPTM1L). Oropharyngeal cancer associations were limited to the human leukocyte antigen (HLA) region, and classical HLA allele imputation showed a protective association with the class II haplotype HLA-DRB1*1301{\textendash}HLA-DQA1*0103{\textendash}HLA-DQB1*0603 (odds ratio (OR) = 0.59, P = 2.7 {\texttimes} 10−9). Stratified analyses on a subgroup of oropharyngeal cases with information available on human papillomavirus (HPV) status indicated that this association was considerably stronger in HPV-positive (OR = 0.23, P = 1.6 {\texttimes} 10−6) than in HPV-negative (OR = 0.75, P = 0.16) cancers.",

keywords = "oral cancer, oral cancer",

author = "Corina Lesseur and Brenda Diergaarde and Olshan, \{Andrew F.\} and Victor W{\"u}nsch-Filho and Ness, \{Andrew R.\} and Geoffrey Liu and Martin Lacko and Jos{\'e} Eluf-Neto and Silvia Franceschi and Pagona Lagiou and Macfarlane, \{Gary J.\} and Lorenzo Richiardi and Stefania Boccia and Jerry Polesel and Kristina Kjaerheim and David Zaridze and Mattias Johansson and Menezes, \{Ana M.\} and Curado, \{Maria Paula\} and Max Robinson and Wolfgang Ahrens and Cristina Canova and Ariana Znaor and Xavier Castellsagu{\'e} and Conway, \{David I.\} and Ivana Holc{\'a}tov{\'a} and Dana Mates and Marta Vilensky and Healy, \{Claire M\} and Neonila Szeszenia-Dabrowska and Eleon{\'o}ra Fabi{\'a}nov{\'a} and Jolanta Lissowska and Grandis, \{Jennifer R.\} and Weissler, \{Mark C.\} and Tajara, \{Eloiza H.\} and Nunes, \{Fabio D.\} and \{De Carvalho\}, \{Marcos B.\} and Steve Thomas and Hung, \{Rayjean J.\} and Peters, \{Wilbert H.M.\} and Rolando Herrero and Gabriella Cadoni and Bueno-De-Mesquita, \{H. Bas\} and Annika Steffen and Antonio Agudo and Oxana Shangina and Xiangjun Xiao and Val{\'e}rie Gaborieau and Am{\'e}lie Chabrier and Devasena Anantharaman and Paolo Boffetta and Amos, \{Christopher I.\} and Mckay, \{James D.\} and Paul Brennan",

year = "2016",

doi = "10.1038/ng.3685",

language = "English",

volume = "2016",

pages = "1544--1550",

journal = "Nature Genetics",

issn = "1061-4036",

publisher = "Nature Research",

}

Lesseur, C, Diergaarde, B, Olshan, AF, Wünsch-Filho, V, Ness, AR, Liu, G, Lacko, M, Eluf-Neto, J, Franceschi, S, Lagiou, P, Macfarlane, GJ, Richiardi, L, Boccia, S, Polesel, J, Kjaerheim, K, Zaridze, D, Johansson, M, Menezes, AM, Curado, MP, Robinson, M, Ahrens, W, Canova, C, Znaor, A, Castellsagué, X, Conway, DI, Holcátová, I, Mates, D, Vilensky, M, Healy, CM, Szeszenia-Dabrowska, N, Fabiánová, E, Lissowska, J, Grandis, JR, Weissler, MC, Tajara, EH, Nunes, FD, De Carvalho, MB, Thomas, S, Hung, RJ, Peters, WHM, Herrero, R, Cadoni, G, Bueno-De-Mesquita, HB, Steffen, A, Agudo, A, Shangina, O, Xiao, X, Gaborieau, V, Chabrier, A, Anantharaman, D, Boffetta, P, Amos, CI, Mckay, JD & Brennan, P 2016, 'Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer.', Nature Genetics, vol. 2016, pagg. 1544-1550. https://doi.org/10.1038/ng.3685

TY - JOUR

T1 - Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer.

AU - Lesseur, Corina

AU - Diergaarde, Brenda

AU - Olshan, Andrew F.

AU - Wünsch-Filho, Victor

AU - Ness, Andrew R.

AU - Liu, Geoffrey

AU - Lacko, Martin

AU - Eluf-Neto, José

AU - Franceschi, Silvia

AU - Lagiou, Pagona

AU - Macfarlane, Gary J.

AU - Richiardi, Lorenzo

AU - Boccia, Stefania

AU - Polesel, Jerry

AU - Kjaerheim, Kristina

AU - Zaridze, David

AU - Johansson, Mattias

AU - Menezes, Ana M.

AU - Curado, Maria Paula

AU - Robinson, Max

AU - Ahrens, Wolfgang

AU - Canova, Cristina

AU - Znaor, Ariana

AU - Castellsagué, Xavier

AU - Conway, David I.

AU - Holcátová, Ivana

AU - Mates, Dana

AU - Vilensky, Marta

AU - Healy, Claire M

AU - Szeszenia-Dabrowska, Neonila

AU - Fabiánová, Eleonóra

AU - Lissowska, Jolanta

AU - Grandis, Jennifer R.

AU - Weissler, Mark C.

AU - Tajara, Eloiza H.

AU - Nunes, Fabio D.

AU - De Carvalho, Marcos B.

AU - Thomas, Steve

AU - Hung, Rayjean J.

AU - Peters, Wilbert H.M.

AU - Herrero, Rolando

AU - Cadoni, Gabriella

AU - Bueno-De-Mesquita, H. Bas

AU - Steffen, Annika

AU - Agudo, Antonio

AU - Shangina, Oxana

AU - Xiao, Xiangjun

AU - Gaborieau, Valérie

AU - Chabrier, Amélie

AU - Anantharaman, Devasena

AU - Boffetta, Paolo

AU - Amos, Christopher I.

AU - Mckay, James D.

AU - Brennan, Paul

PY - 2016

Y1 - 2016

N2 - We conducted a genome-wide association study of oral cavity and pharyngeal cancer in 6,034 cases and 6,585 controls from Europe, North America and South America. We detected eight significantly associated loci (P < 5 × 10−8), seven of which are new for these cancer sites. Oral and pharyngeal cancers combined were associated with loci at 6p21.32 (rs3828805, HLA-DQB1), 10q26.13 (rs201982221, LHPP) and 11p15.4 (rs1453414, OR52N2–TRIM5). Oral cancer was associated with two new regions, 2p23.3 (rs6547741, GPN1) and 9q34.12 (rs928674, LAMC3), and with known cancer-related loci—9p21.3 (rs8181047, CDKN2B-AS1) and 5p15.33 (rs10462706, CLPTM1L). Oropharyngeal cancer associations were limited to the human leukocyte antigen (HLA) region, and classical HLA allele imputation showed a protective association with the class II haplotype HLA-DRB1*1301–HLA-DQA1*0103–HLA-DQB1*0603 (odds ratio (OR) = 0.59, P = 2.7 × 10−9). Stratified analyses on a subgroup of oropharyngeal cases with information available on human papillomavirus (HPV) status indicated that this association was considerably stronger in HPV-positive (OR = 0.23, P = 1.6 × 10−6) than in HPV-negative (OR = 0.75, P = 0.16) cancers.

AB - We conducted a genome-wide association study of oral cavity and pharyngeal cancer in 6,034 cases and 6,585 controls from Europe, North America and South America. We detected eight significantly associated loci (P < 5 × 10−8), seven of which are new for these cancer sites. Oral and pharyngeal cancers combined were associated with loci at 6p21.32 (rs3828805, HLA-DQB1), 10q26.13 (rs201982221, LHPP) and 11p15.4 (rs1453414, OR52N2–TRIM5). Oral cancer was associated with two new regions, 2p23.3 (rs6547741, GPN1) and 9q34.12 (rs928674, LAMC3), and with known cancer-related loci—9p21.3 (rs8181047, CDKN2B-AS1) and 5p15.33 (rs10462706, CLPTM1L). Oropharyngeal cancer associations were limited to the human leukocyte antigen (HLA) region, and classical HLA allele imputation showed a protective association with the class II haplotype HLA-DRB1*1301–HLA-DQA1*0103–HLA-DQB1*0603 (odds ratio (OR) = 0.59, P = 2.7 × 10−9). Stratified analyses on a subgroup of oropharyngeal cases with information available on human papillomavirus (HPV) status indicated that this association was considerably stronger in HPV-positive (OR = 0.23, P = 1.6 × 10−6) than in HPV-negative (OR = 0.75, P = 0.16) cancers.

KW - oral cancer

UR - http://hdl.handle.net/10807/92831

U2 - 10.1038/ng.3685

DO - 10.1038/ng.3685

M3 - Article

SN - 1061-4036

VL - 2016

SP - 1544

EP - 1550

JO - Nature Genetics

JF - Nature Genetics

ER -

Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer.

Abstract

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