Recent advances in understanding of interactions between genes and diet in the etiology of colorectal cancer

被引:9
作者
Ferguson, Lynnette R. [1 ]
机构
[1] Univ Auckland, Discipline Nutr, Private Bag 92019, Auckland, New Zealand
关键词
Transforming growth factor beta; Colorectal; GENOME-WIDE ASSOCIATION; GROWTH-FACTOR-BETA; SUSCEPTIBILITY LOCUS; VITAMIN-D; POLYMORPHISMS; RISK; METAANALYSIS; MUTAGENS; PATHWAY; MEAT;
D O I
10.4251/wjgo.v2.i3.125
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
At an international level, colorectal cancer (CRC) is a major cause of morbidity and mortality. Diet plays a major etiologic role, and a range of putative dietary carcinogens have been identified. The probability with which these lead to mutations, and thereby cause cancer, is strongly impacted by variants in genes coding for xenobiotic metabolizing or DNA repair enzymes. Nutrient deficiencies also play a role, which will be exacerbated by variants in metabolic genes. However, many of the causal genes in sporadic CRC have hitherto proved elusive. The power of large international collabo-rations, coupled with genome-wide association studies, has implicated a major functional role of the tumour growth factor-beta pathway in CRC susceptibility. Nutrient regulation of gene expression may be especially important here. Future large collaborative studies must consider gene-gene and gene-diet interactions, coupled with high throughput genomic technologies, in order to uncover the relative roles of genetic variants, mutagenic xenobiotics, nutrient imbalance and gene expression in the etiology of CRC. (C) 2010 Baishideng. All rights reserved.
引用
收藏
页码:125 / 129
页数:5
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