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Grant Details

Grant Number: 5R21CA191312-02 Interpret this number
Primary Investigator: Hsu, Li
Organization: Fred Hutchinson Cancer Research Center
Project Title: Using Functional Data to Reveal Gene-Environment Interaction in Colorectal Cancer
Fiscal Year: 2016


Abstract

DESCRIPTION (provided by applicant): Colorectal cancer (CRC) is the third most common cancer and the second-leading cause of cancer death in the United States. Both genetic (G) and environmental (E) factors play important roles in CRC. It is thus important to study the interplay between G and E to better understand the etiology of this complex disease. The recent availability of genome-wide genotype data and advances in statistical methods has enabled agnostic genome-wide searches for gene-environment interaction (GxE), which have identified several novel interactions. Despite these successes, limited statistical power remains a primary concern in GxE analysis as the sample size required to detect interactions is at least 4x that required to detect main effects of similar magnitude. This limitation is particularly relevant following stringent correction for multiple tests in genome- wide GxE analysis. Further, despite the potential importance of rare variants in CRC, existing GxE studies focus on common variants. We thus propose to use functional data to inform GxE testing for both common and rare variants across the genome. We will apply novel statistical methods to aggregate interaction signals among a set of G's or a set of E's to increase power. We will leverage the existing resources in the Genetics and Epidemiology of Colorectal Cancer Consortium and the Colon Cancer Family Registry, in which genetic and well harmonized environmental data are available for close to 40,000 CRC cases and controls. In addition, we are currently building a CRC-specific functional annotation database based on >80 annotation datasets across public databases such as UCSC Genome Browser, ENCODE, NIH Roadmap, GTEx, and TCGA. In Aim 1, we will examine whether common variants (MAF>1%) predicted in silico to have functional importance modify the effect of environmental risk factors on CRC risk. By prioritizing functional candidates for GxE testing, we will greatly reduce the multiple testing burden that arises from testing millions of SNPs across the genome. In Aim 2, we will perform aggregate association testing to examine interactions between rare variants (MAF<1%) and environmental risk factors for CRC. Functional information will be used to give greater weights to biologically important variants when aggregating interaction signals. In Aim 3, we will test GxE for an aggregated set of environmental variables that capture different components of a single environmental risk factor (e.g., for smoking the components include current/ever/never use, dose, and duration). As these may influence CRC in distinct ways, we will aggregate the interaction signals across components, which will increase power to detect GxE. Overall, the proposed study provides a unique opportunity to detect novel GxE findings for CRC risk-particularly for functionally important or rare variants across the genome. We expect that our findings will help provide a better understanding of the interplay between genetic and environmental factors in CRC development. By identifying carcinogenic mechanisms and, in turn, potential targets for future therapies, these insights can help improve current prevention and treatment strategies for CRC.



Publications

Genetic architectures of proximal and distal colorectal cancer are partly distinct.
Authors: Huyghe J.R. , Harrison T.A. , Bien S.A. , Hampel H. , Figueiredo J.C. , Schmit S.L. , Conti D.V. , Chen S. , Qu C. , Lin Y. , et al. .
Source: Gut, 2021 Jul; 70(7), p. 1325-1334.
EPub date: 2021-02-25.
PMID: 33632709
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Circulating adipokine concentrations and risk of five obesity-related cancers: A Mendelian randomization study.
Authors: Dimou N.L. , Papadimitriou N. , Mariosa D. , Johansson M. , Brennan P. , Peters U. , Chanock S.J. , Purdue M. , Bishop D.T. , Gago-Dominquez M. , et al. .
Source: International journal of cancer, 2021-04-01; 148(7), p. 1625-1636.
EPub date: 2020-10-26.
PMID: 33038280
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A Combined Proteomics and Mendelian Randomization Approach to Investigate the Effects of Aspirin-Targeted Proteins on Colorectal Cancer.
Authors: Nounu A. , Greenhough A. , Heesom K.J. , Richmond R.C. , Zheng J. , Weinstein S.J. , Albanes D. , Baron J.A. , Hopper J.L. , Figueiredo J.C. , et al. .
Source: Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2021 03; 30(3), p. 564-575.
EPub date: 2020-12-14.
PMID: 33318029
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Identifying Novel Susceptibility Genes for Colorectal Cancer Risk From a Transcriptome-Wide Association Study of 125,478 Subjects.
Authors: Guo X. , Lin W. , Wen W. , Huyghe J. , Bien S. , Cai Q. , Harrison T. , Chen Z. , Qu C. , Bao J. , et al. .
Source: Gastroenterology, 2021 03; 160(4), p. 1164-1178.e6.
EPub date: 2020-10-12.
PMID: 33058866
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Adiposity, metabolites, and colorectal cancer risk: Mendelian randomization study.
Authors: Bull C.J. , Bell J.A. , Murphy N. , Sanderson E. , Davey Smith G. , Timpson N.J. , Banbury B.L. , Albanes D. , Berndt S.I. , Bézieau S. , et al. .
Source: BMC medicine, 2020-12-17; 18(1), p. 396.
EPub date: 2020-12-17.
PMID: 33327948
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Intake of Dietary Fruit, Vegetables, and Fiber and Risk of Colorectal Cancer According to Molecular Subtypes: A Pooled Analysis of 9 Studies.
Authors: Hidaka A. , Harrison T.A. , Cao Y. , Sakoda L.C. , Barfield R. , Giannakis M. , Song M. , Phipps A.I. , Figueiredo J.C. , Zaidi S.H. , et al. .
Source: Cancer research, 2020-10-15; 80(20), p. 4578-4590.
EPub date: 2020-08-14.
PMID: 32816852
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Identification of Novel Loci and New Risk Variant in Known Loci for Colorectal Cancer Risk in East Asians.
Authors: Lu Y. , Kweon S.S. , Cai Q. , Tanikawa C. , Shu X.O. , Jia W.H. , Xiang Y.B. , Huyghe J.R. , Harrison T.A. , Kim J. , et al. .
Source: Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2020 02; 29(2), p. 477-486.
EPub date: 2019-12-11.
PMID: 31826910
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Discovery of common and rare genetic risk variants for colorectal cancer.
Authors: Huyghe J.R. , Bien S.A. , Harrison T.A. , Kang H.M. , Chen S. , Schmit S.L. , Conti D.V. , Qu C. , Jeon J. , Edlund C.K. , et al. .
Source: Nature genetics, 2019 01; 51(1), p. 76-87.
EPub date: 2018-12-03.
PMID: 30510241
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A unified powerful set-based test for sequencing data analysis of GxE interactions.
Authors: Su Y.R. , Di C.Z. , Hsu L. , Genetics and Epidemiology of Colorectal Cancer Consortium .
Source: Biostatistics (Oxford, England), 2017 01; 18(1), p. 119-131.
EPub date: 2016-07-28.
PMID: 27474101
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Powerful Set-Based Gene-Environment Interaction Testing Framework for Complex Diseases.
Authors: Jiao S. , Peters U. , Berndt S. , Bézieau S. , Brenner H. , Campbell P.T. , Chan A.T. , Chang-Claude J. , Lemire M. , Newcomb P.A. , et al. .
Source: Genetic epidemiology, 2015 Dec; 39(8), p. 609-18.
EPub date: 2015-06-10.
PMID: 26095235
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SBERIA: set-based gene-environment interaction test for rare and common variants in complex diseases.
Authors: Jiao S. , Hsu L. , Bézieau S. , Brenner H. , Chan A.T. , Chang-Claude J. , Le Marchand L. , Lemire M. , Newcomb P.A. , Slattery M.L. , et al. .
Source: Genetic epidemiology, 2013 Jul; 37(5), p. 452-64.
EPub date: 2013-05-29.
PMID: 23720162
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