Interleukin genes and associations with colon and rectal cancer risk and overall survival

被引:71
作者
Bondurant, Kristina L. [1 ]
Lundgreen, Abbie [2 ]
Herrick, Jennifer S. [2 ]
Kadlubar, Susan [3 ]
Wolff, Roger K. [2 ]
Slattery, Martha L. [2 ]
机构
[1] Univ Arkansas Med Sci, Dept Environm & Occupat Hlth, Little Rock, AR 72205 USA
[2] Univ Utah, Dept Internal Med, Hlth Sci Ctr, Salt Lake City, UT 84112 USA
[3] Univ Arkansas Med Sci, Div Genet, Little Rock, AR 72205 USA
关键词
interleukins; colon cancer; rectal cancer; single nucleotide polymorphisms; inflammatory; INFLAMMATORY-BOWEL-DISEASE; SINGLE-NUCLEOTIDE POLYMORPHISMS; ULCERATIVE-COLITIS; COLORECTAL-CANCER; CROHNS-DISEASE; RECEPTOR ANTAGONIST; COMMON POLYMORPHISMS; CORRELATED RESPONSES; SIGNALING PATHWAY; PHYSICAL-ACTIVITY;
D O I
10.1002/ijc.27660
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Interleukins are a group of cytokines that contribute to growth and differentiation, cell migration, and inflammatory and anti-inflammatory responses by the immune system. In our study, we examined genetic variation in genes from various anti-inflammatory and proinflammatory interleukins to determine association with colon and rectal cancer risk and overall survival. Data from two population-based incident studies of colon cancer (1,555 cases and 1,956 controls) and rectal cancer (754 cases and 954 controls) were used. After controlling for multiple comparisons, single nucleotide polymorphisms (SNPs) from four genes, IL3, IL6R, IL8, IL15, were associated with increased colon cancer risk, and CXCR1 and CXCR2 were significantly associated with increased rectal cancer risk. Only SNPs from genes within the IL-8 pathway (IL8, CXCR1 and CXCR2) showed a significant association with both colon and rectal cancer risk. Several SNPs interacted significantly with IL8 and IFNG SNPs and with aspirin/non-steroidal anti-inflammatory drug (NSAID), cigarette smoking, estrogen use and BMI. For both colon and rectal cancer, increasing numbers of risk alleles were associated with increased hazard of death from cancer; the estimated hazard of death for colon cancer for the highest category of risk alleles was 1.74 (95% confidence interval [CI] 1.18-2.56) and 1.96 (95% CI 1.28-2.99) for rectal cancer. These data suggest that interleukin genes play a role in risk and overall survival for colon and rectal cancer.
引用
收藏
页码:905 / 915
页数:11
相关论文
共 47 条
[1]   Association of single nucleotide polymorphisms in the interleukin-4 gene and interleukin-4 receptor gene with Crohn's disease in a British population [J].
Aithal, GP ;
Day, CP ;
Leathart, J ;
Daly, AK ;
Hudson, M .
GENES AND IMMUNITY, 2001, 2 (01) :44-47
[2]   The polymorphism rs3024505 proximal to IL-10 is associated with risk of ulcerative colitis and Crohns disease in a Danish case-control study [J].
Andersen, Vibeke ;
Ernst, Anja ;
Christensen, Jane ;
Ostergaard, Mette ;
Jacobsen, Bent A. ;
Tjonneland, Anne ;
Krarup, Henrik B. ;
Vogel, Ulla .
BMC MEDICAL GENETICS, 2010, 11
[3]   Inflammatory bowel disease: the role of inflammatory cytokine gene polymorphisms [J].
Balding, J ;
Livingstone, WJ ;
Conroy, J ;
Mynett-Johnson, L ;
Weir, DG ;
Mahmud, N ;
Smith, OP .
MEDIATORS OF INFLAMMATION, 2004, 13 (03) :181-187
[4]   Evidence for genetic heterogeneity in IBD .1. The interleukin-2 receptor antagonist in the predisposition to suffer from ulcerative colitis [J].
Bioque, G ;
Bouma, G ;
Crusius, JBA ;
Koutroubakis, I ;
Kostense, PJ ;
Meuwissen, SGM ;
Pena, AS .
EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY, 1996, 8 (02) :105-110
[5]  
Burton P, 1998, STAT MED, V17, P1261, DOI 10.1002/(SICI)1097-0258(19980615)17:11<1261::AID-SIM846>3.0.CO
[6]  
2-Z
[7]   Influence of interleukin-8 and interleukin-10 on sporadic colon cancer development and progression [J].
Cacev, Tamara ;
Radosevic, Senka ;
Krizanac, Simun ;
Kapitanovic, Sanja .
CARCINOGENESIS, 2008, 29 (08) :1572-1580
[8]   Identification of pathway-selective estrogen receptor ligands that inhibit NF-κ3 transcriptional activity [J].
Chadwick, CC ;
Chippari, S ;
Matelan, E ;
Borges-Marcucci, L ;
Eckert, AM ;
Keith, JC ;
Albert, LM ;
Leathurby, Y ;
Harris, HA ;
Bhat, RA ;
Ashwell, M ;
Trybulski, E ;
Winneker, RC ;
Adeknab, SJ ;
Steffan, RJ ;
Harnish, DC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (07) :2543-2548
[9]   Contribution of the novel inflammatory bowel disease gene IL23R to disease susceptibility and phenotype [J].
Cummings, J. A. Fraser ;
Ahmad, Tariq ;
Geremia, Alessandra ;
Beckly, John ;
Cooney, Rachel ;
Hancock, Laura ;
Pathan, Saad ;
Guo, Changcun ;
Cardon, Lon R. ;
Jewell, Derek P. .
INFLAMMATORY BOWEL DISEASES, 2007, 13 (09) :1063-1068
[10]   Sex hormones influence on the immune system: basic and clinical aspects in autoimmunity [J].
Cutolo, M ;
Sulli, A ;
Capellino, S ;
Villaggio, B ;
Montagna, P ;
Seriolo, B ;
Straub, RH .
LUPUS, 2004, 13 (09) :635-638