Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/204381
Title: A Genetic Locus within the FMN1/GREM1 Gene Region Interacts with Body Mass Index in Colorectal Cancer Risk
Author: Aglago, Elom K.
Kim, Andre
Lin, Yi
Qu, Conghui
Evangelou, Marina
Ren, Yu
Morrison, John
Albanes, Demetrius
Arndt, Volker
Barry, Elizabeth L.
Baurley, James W.
Berndt, Sonja I.
Bien, Stephanie A.
Bishop, D. Timothy
Bouras, Emmanouil
Brenner, Hermann
Buchanan, Daniel D.
Budiarto, Arif
Carreras Torres, Robert
Casey, Graham
Cenggoro, Wawan Tjeng
Chan, Andrew T.
Chang-Claude, Jenny
Chen, Xuechen
Conti, David V.
Devall, Matthew
Díez Obrero, Virginia
Dimou, Niki
Drew, David
Figueiredo, Jane C.
Gallinger, Steven
Giles, Graham G.
Gruber, Stephen B.
Gsur, Andrea
Gunter, Marc J.
Hampel, Heather
Harlid, Sophia
Hidaka, Akihisa
Harrison, Tabitha A.
Hoffmeister, Michael
Huyghe, Jeroen R.
Jenkins, Mark A.
Jordahl, Kristina
Joshi, Amit D.
Kawaguchi, Eric S.
Keku, Temitope O.
Kundaje, Anshul
Larsson, Susanna C.
Marchand, Loic Le
Lewinger, Juan Pablo
Li, Li
Lynch, Brigid M.
Mahesworo, Bharuno
Mandic, Marko
Obón Santacana, Mireia
Moreno Aguado, Víctor
Murphy, Neil
Nan, Hongmei
Nassir, Rami
Newcomb, Polly A.
Ogino, Shuji
Ose, Jennifer
Pai, Rish K.
Palmer, Julie R.
Papadimitriou, Nikos
Pardamean, Bens
Peoples, Anita R.
Platz, Elizabeth A.
Potter, John D.
Prentice, Ross L.
Rennert, Gad
Ruiz-Narvaez, Edward
Sakoda, Lori C.
Scacheri, Peter C.
Schmit, Stephanie L.
Schoen, Robert E.
Shcherbina, Anna
Slattery, Martha L.
Stern, Mariana C.
Su, Yu Ru
Tangen, Catherine M.
Thibodeau, Stephen N.
Thomas, Duncan C.
Tian, Yu
Ulrich, Cornelia M.
Duijnhoven, Franzel J.B. van
Guelpen, Bethany van
Visvanathan, Kala
Vodicka, Pavel
Wang, Jun
White, Emily
Wolk, Alicja
Woods, Michael O.
Wu, Anna H.
Zemlianskaia, Natalia
Hsu, Li
Gauderman, W. James
Peters, Ulrike
Tsilidis, Konstantinos K.
Campbell, Peter T.
Keywords: Càncer colorectal
Obesitat
Colorectal cancer
Obesity
Issue Date: 30-May-2023
Publisher: American Association for Cancer Research (AACR)
Abstract: Colorectal cancer risk can be impacted by genetic, environmental, and lifestyle factors, including diet and obesity. Geneenvironment interactions (G x E) can provide biological insights into the effects of obesity on colorectal cancer risk. Here, we assessed potential genome-wide G x E interactions between body mass index (BMI) and common SNPs for colorectal cancer risk using data from 36,415 colorectal cancer cases and 48,451 controls from three international colorectal cancer consortia (CCFR, CORECT, and GECCO). The G x E tests included the conventional logistic regression using multiplicative terms (one degree of freedom, 1DF test), the two-step EDGE method, and the joint 3DF test, each of which is powerful for detecting G x E interactions under specific conditions. BMI was associated with higher colorectal cancer risk. The two-step approach revealed a statistically significant GxBMI interaction located within the Formin 1/Gremlin 1 (FMN1/GREM1) gene region (rs58349661). This SNP was also identified by the 3DF test, with a suggestive statistical significance in the 1DF test. Among participants with the CC genotype of rs58349661, overweight and obesity categories were associated with higher colorectal cancer risk, whereas null associations were observed across BMI categories in those with the TT genotype. Using data from three large international consortia, this study discovered a locus in the FMN1/GREM1 gene region that interacts with BMI on the association with colorectal cancer risk. Further studies should examine the potential mechanisms through which this locus modifies the etiologic link between obesity and colorectal cancer.
Note: Reproducció del document publicat a: https://doi.org/10.1158/0008-5472.CAN-22-3713
It is part of: Cancer Research, 2023, vol. 83, num. 15, p. 2572-2583
URI: http://hdl.handle.net/2445/204381
Related resource: https://doi.org/10.1158/0008-5472.CAN-22-3713
ISSN: 1538-7445
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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