Genetic determinants of telomere length and risk of pancreatic cancer: A PANDoRA study

被引:44
|
作者
Campa, Daniele [1 ]
Matarazzi, Martina [1 ,2 ]
Greenhalf, William [3 ]
Bijlsma, Maarten [4 ]
Saum, Kai-Uwe [5 ]
Pasquali, Claudio [6 ]
van Laarhoven, Hanneke [4 ]
Szentesi, Andrea [7 ,8 ]
Federici, Francesca [9 ]
Vodicka, Pavel [10 ,11 ,12 ]
Funel, Niccola [13 ]
Pezzilli, Raffaele [14 ]
Bueno-de-Mesquita, H. Bas [15 ,16 ,17 ,18 ]
Vodickova, Ludmila [10 ,11 ,12 ]
Basso, Daniela [19 ]
Obazee, Ofure [2 ]
Hackert, Thilo [20 ]
Soucek, Pavel [12 ]
Cuk, Katarina [5 ]
Kaiser, Joerg [20 ]
Sperti, Cosimo [23 ]
Lovecek, Martin [21 ,22 ]
Capurso, Gabriele [24 ,25 ]
Mohelnikova-Duchonova, Beatrice [26 ]
Khaw, Kay-Tee [27 ]
Koenig, Anna-Katharina [20 ]
Kupcinskas, Juozas [28 ]
Kaaks, Rudolf [29 ]
Bambi, Franco [30 ]
Archibugi, Livia [24 ,25 ]
Mambrini, Andrea [9 ]
Cavestro, Giulia Martina [31 ]
Landi, Stefano [1 ]
Hegyi, Peter [7 ,8 ,32 ]
Izbicki, Jakob R. [33 ]
Gioffreda, Domenica [34 ,35 ]
Zambon, Carlo Federico [23 ]
Tavano, Francesca [34 ,35 ]
Talar-Wojnarowska, Renata [36 ]
Jamroziak, Krzysztof [37 ]
Key, Timothy J. [38 ]
Delle Fave, Gianfranco [24 ]
Strobel, Oliver [20 ]
Jonaitis, Laimas [28 ]
Andriulli, Angelo [34 ,35 ]
Lawlor, Rita T. [39 ]
Pirozzi, Felice [40 ]
Katzke, Verena [29 ]
Valsuani, Chiara [9 ]
Vashist, Yogesh K. [33 ]
机构
[1] Univ Pisa, Dept Biol, Pisa, Italy
[2] German Canc Res Ctr, Genom Epidemiol Grp, Neuenheimer Feld 280, D-69120 Heidelberg, Germany
[3] Univ Liverpool, Liverpool Pancreas Biomed Res Unit, Inst Hlth Res, Liverpool, Merseyside, England
[4] Acad Med Ctr, Med Oncol, Amsterdam, Netherlands
[5] German Canc Res Ctr, Div Clin Epidemiol & Aging Res, Heidelberg, Germany
[6] Univ Padua, Dept Surg Oncol & Gastroenterol DiSCOG, Pancreat & Digest Endocrine Surg, Padua, Italy
[7] Univ Pecs, Inst Translat Med, Pecs, Hungary
[8] Univ Szeged, Dept Med 1, Szeged, Hungary
[9] Azienda USL Toscana Nord Ovest, Oncol Unit Massa Carrara, Oncol Dept, Carrara, Italy
[10] Acad Sci Czech Republ, Inst Expt Med, Dept Mol Biol Canc, Prague, Czech Republic
[11] Charles Univ Prague, Med Fac 1, Inst Biol & Med Genet, Prague, Czech Republic
[12] Charles Univ Prague, Fac Med Pilsen, Biomed Ctr, Plzen, Czech Republic
[13] Univ Pisa, Unit Expt Surg Pathol, Dept Surg, Pisa, Italy
[14] St Orsola Malpighi Hosp, Dept Digest Syst, Pancreas Unit, Bologna, Italy
[15] Natl Inst Publ Hlth & Environm RIVM, Dept Determinants Chron Dis DCD, Bilthoven, Netherlands
[16] Univ Med Ctr, Dept Gastroenterol & Hepatol, Utrecht, Netherlands
[17] Imperial Coll London, Sch Publ Hlth, Dept Epidemiol & Biostat, London, England
[18] Univ Malaya, Fac Med, Dept Social & Prevent Med, Kuala Lumpur, Malaysia
[19] Univ Hosp Padova, Dept Lab Med, Padua, Italy
[20] Univ Hosp Heidelberg, Dept Gen Visceral & Transplantat Surg, Heidelberg, Germany
[21] Palacky Univ Olomouc, Fac Med & Dent, Dept Surg 1, Olomouc, Czech Republic
[22] Univ Hosp Olomouc, Olomouc, Czech Republic
[23] Univ Padua, Surg Clin Dept Surg 3, Dept Surg Oncol & Gastroenterol DiSCOG, Padua, Italy
[24] Sapienza Univ, S Andrea Hosp, Digest & Liver Dis Unit, Rome, Italy
[25] Univ Vita Salute San Raffaele, IRCCS San Raffaele Sci Inst, Pancreas Translat & Clin Res Ctr, PancreatoBiliary Endoscopy & EUS Div, Milan, Italy
[26] Palacky Univ, Fac Med & Dent, Inst Mol & Translat Med, Dept Oncol, Olomouc, Czech Republic
[27] Univ Cambridge, Addenbrookes Hosp, Sch Clin Med, Clin Gerontol Unit, Cambridge, England
[28] Lithuanian Univ Hlth Sci, Dept Gastroenterol, Kaunas, Lithuania
[29] German Canc Res Ctr, Div Canc Epidemiol, Heidelberg, Germany
[30] Azienda Osped Univ Meyer, Blood Transfus Serv, Florence, Italy
[31] Univ Vita Salute San Raffaele, San Raffaele Sci Inst, Gastroenterol & Gastrointestinal Endoscopy Unit, Milan, Italy
[32] MTA SZTE Momentum Translat Gastroenterol Res Grp, Szeged, Hungary
[33] Univ Med Ctr Hamburg Eppendorf, Dept Gen Visceral & Thorac Surg, Hamburg, Germany
[34] IRCCS Osped Casa Sollievo Sofferenza, Div Gastroenterol, San Giovanni Rotondo, Italy
[35] IRCCS Osped Casa Sollievo Sofferenza, Mol Biol Lab, San Giovanni Rotondo, Italy
[36] Med Univ Lodz, Dept Digest Tract Dis, Lodz, Poland
[37] Inst Hematol & Transfus Med, Warsaw, Poland
[38] Univ Oxford, Nuffield Dept Populat Hlth, Canc Epidemiol Unit, Oxford, England
[39] Univ & Hosp Trust Verona, ARC NET, Verona, Italy
[40] IRCCS Osped Casa Sollievo Sofferenza, Div Abdominal Surg, San Giovanni Rotondo, Italy
[41] German Canc Res Ctr, Div Prevent Oncol, Heidelberg, Germany
[42] Natl Ctr Tumor Dis NCT, Heidelberg, Germany
[43] German Canc Res Ctr, German Canc Consortium DKTK, Heidelberg, Germany
关键词
pancreatic ductal adenocarcinoma; genetic polymorphisms; lymphocyte telomere length; Mendelian randomization; association; GENOME-WIDE ASSOCIATION; SUSCEPTIBILITY LOCI; POLYMORPHISMS; VARIANTS; DISEASE; LONGER; SURVIVAL; TERT;
D O I
10.1002/ijc.31928
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Telomere deregulation is a hallmark of cancer. Telomere length measured in lymphocytes (LTL) has been shown to be a risk marker for several cancers. For pancreatic ductal adenocarcinoma (PDAC) consensus is lacking whether risk is associated with long or short telomeres. Mendelian randomization approaches have shown that a score built from SNPs associated with LTL could be used as a robust risk marker. We explored this approach in a large scale study within the PANcreatic Disease ReseArch (PANDoRA) consortium. We analyzed 10 SNPs (ZNF676-rs409627, TERT-rs2736100, CTC1-rs3027234, DHX35-rs6028466, PXK-rs6772228, NAF1-rs7675998, ZNF208-rs8105767, OBFC1-rs9420907, ACYP2-rs11125529 and TERC-rs10936599) alone and combined in a LTL genetic score ("teloscore", which explains 2.2% of the telomere variability) in relation to PDAC risk in 2,374 cases and 4,326 controls. We identified several associations with PDAC risk, among which the strongest were with the TERT-rs2736100 SNP (OR = 1.54; 95%CI 1.35-1.76; p = 1.54 x 10(-10)) and a novel one with the NAF1-rs7675998 SNP (OR = 0.80; 95%CI 0.73-0.88; p = 1.87 x 10(-6), p(trend) = 3.27 x 10(-7)). The association of short LTL, measured by the teloscore, with PDAC risk reached genome-wide significance (p = 2.98 x 10(-9) for highest vs. lowest quintile; p = 1.82 x 10(-10) as a continuous variable). In conclusion, we present a novel genome-wide candidate SNP for PDAC risk (TERT-rs2736100), a completely new signal (NAF1-rs7675998) approaching genome-wide significance and we report a strong association between the teloscore and risk of pancreatic cancer, suggesting that telomeres are a potential risk factor for pancreatic cancer.
引用
收藏
页码:1275 / 1283
页数:9
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