Literature DB >> 31884074

Circulating Levels of Insulin-like Growth Factor 1 and Insulin-like Growth Factor Binding Protein 3 Associate With Risk of Colorectal Cancer Based on Serologic and Mendelian Randomization Analyses.

Neil Murphy1, Robert Carreras-Torres2, Mingyang Song3, Andrew T Chan4, Richard M Martin5, Nikos Papadimitriou6, Niki Dimou6, Konstantinos K Tsilidis7, Barbara Banbury8, Kathryn E Bradbury9, Jelena Besevic10, Sabina Rinaldi6, Elio Riboli10, Amanda J Cross10, Ruth C Travis11, Claudia Agnoli12, Demetrius Albanes13, Sonja I Berndt13, Stéphane Bézieau14, D Timothy Bishop15, Hermann Brenner16, Daniel D Buchanan17, N Charlotte Onland-Moret18, Andrea Burnett-Hartman19, Peter T Campbell20, Graham Casey21, Sergi Castellví-Bel22, Jenny Chang-Claude23, María-Dolores Chirlaque24, Albert de la Chapelle25, Dallas English26, Jane C Figueiredo27, Steven J Gallinger28, Graham G Giles29, Stephen B Gruber30, Andrea Gsur31, Jochen Hampe32, Heather Hampel33, Tabitha A Harrison8, Michael Hoffmeister34, Li Hsu35, Wen-Yi Huang13, Jeroen R Huyghe8, Mark A Jenkins36, Temitope O Keku37, Tilman Kühn23, Sun-Seog Kweon38, Loic Le Marchand39, Christopher I Li8, Li Li40, Annika Lindblom41, Vicente Martín42, Roger L Milne29, Victor Moreno43, Polly A Newcomb44, Kenneth Offit45, Shuji Ogino46, Jennifer Ose47, Vittorio Perduca48, Amanda I Phipps49, Elizabeth A Platz50, John D Potter51, Conghui Qu8, Gad Rennert52, Lori C Sakoda53, Clemens Schafmayer54, Robert E Schoen55, Martha L Slattery56, Catherine M Tangen57, Cornelia M Ulrich47, Franzel J B van Duijnhoven58, Bethany Van Guelpen59, Kala Visvanathan50, Pavel Vodicka60, Ludmila Vodickova60, Veronika Vymetalkova60, Hansong Wang39, Emily White49, Alicja Wolk61, Michael O Woods62, Anna H Wu63, Wei Zheng64, Ulrike Peters49, Marc J Gunter6.   

Abstract

BACKGROUND & AIMS: Human studies examining associations between circulating levels of insulin-like growth factor 1 (IGF1) and insulin-like growth factor binding protein 3 (IGFBP3) and colorectal cancer risk have reported inconsistent results. We conducted complementary serologic and Mendelian randomization (MR) analyses to determine whether alterations in circulating levels of IGF1 or IGFBP3 are associated with colorectal cancer development.
METHODS: Serum levels of IGF1 were measured in blood samples collected from 397,380 participants from the UK Biobank, from 2006 through 2010. Incident cancer cases and cancer cases recorded first in death certificates were identified through linkage to national cancer and death registries. Complete follow-up was available through March 31, 2016. For the MR analyses, we identified genetic variants associated with circulating levels of IGF1 and IGFBP3. The association of these genetic variants with colorectal cancer was examined with 2-sample MR methods using genome-wide association study consortia data (52,865 cases with colorectal cancer and 46,287 individuals without [controls])
RESULTS: After a median follow-up period of 7.1 years, 2665 cases of colorectal cancer were recorded. In a multivariable-adjusted model, circulating level of IGF1 associated with colorectal cancer risk (hazard ratio per 1 standard deviation increment of IGF1, 1.11; 95% confidence interval [CI] 1.05-1.17). Similar associations were found by sex, follow-up time, and tumor subsite. In the MR analyses, a 1 standard deviation increment in IGF1 level, predicted based on genetic factors, was associated with a higher risk of colorectal cancer risk (odds ratio 1.08; 95% CI 1.03-1.12; P = 3.3 × 10-4). Level of IGFBP3, predicted based on genetic factors, was associated with colorectal cancer risk (odds ratio per 1 standard deviation increment, 1.12; 95% CI 1.06-1.18; P = 4.2 × 10-5). Colorectal cancer risk was associated with only 1 variant in the IGFBP3 gene region (rs11977526), which also associated with anthropometric traits and circulating level of IGF2.
CONCLUSIONS: In an analysis of blood samples from almost 400,000 participants in the UK Biobank, we found an association between circulating level of IGF1 and colorectal cancer. Using genetic data from 52,865 cases with colorectal cancer and 46,287 controls, a higher level of IGF1, determined by genetic factors, was associated with colorectal cancer. Further studies are needed to determine how this signaling pathway might contribute to colorectal carcinogenesis.
Copyright © 2020 AGA Institute. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  CRC; GWAS; Risk Factors; Signal Transduction

Mesh:

Substances:

Year:  2019        PMID: 31884074      PMCID: PMC7152801          DOI: 10.1053/j.gastro.2019.12.020

Source DB:  PubMed          Journal:  Gastroenterology        ISSN: 0016-5085            Impact factor:   22.682


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