4.7 Article

Association of apolipoprotein E polymorphisms and dietary factors in colorectal cancer

期刊

BRITISH JOURNAL OF CANCER
卷 100, 期 12, 页码 1966-1974

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/sj.bjc.6605097

关键词

CRC: colorectal cancer; ApoE: apolipoprotein E; MMR: mismatch repair; MSI-H: high-frequency microsatellite instability; MSS/L: microsatellite stable/low-frequency microsatellite instability; SNP: single nucleotide polymorphism

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资金

  1. American Institute for Cancer Research [99B055]
  2. Canadian Institutes of Health Research [MOP43950]
  3. National Cancer Institute
  4. National Institutes of Health under Request For Applications [CA-95-011]
  5. Ontario Registry for Studies of Familial Colorectal Cancer [U01 CA074783]
  6. National Cancer Institute of Canada [018668]
  7. Samuel Lunenfeld Research Institute
  8. Team in Interdisciplinary Research in Colorectal Cancer
  9. Canadian Institutes of Health Research

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ApoE single nucleotide polymorphisms (SNPs) Cys112Arg (Epsilon-4), and Arg158Cys (Epsilon-2) have been implicated in cardiovascular and Alzheimer's disease, but their role in colorectal cancer (CRC) has not been extensively studied. We investigated whether ApoE polymorphisms alone or in combination with dietary factors selectively contribute to mismatch-repair (MMR) proficient (microsatellite stable/low or MSS/L) vs deficient (microsatellite unstable or MSI-H) CRCs. We carried out a case-control study with 906 CRC cases and 911 unaffected controls to examine the associations between ApoE polymorphisms and dietary factors and assessed their contribution to MSS/L and MSI-H CRCs. We used unconditional logistic regression to evaluate the associations between ApoE SNPs, tumour MSI status, and dietary factors after adjusting for age and sex. All statistical tests were two-sided. No significant differences in ApoE genotype frequencies were observed between CRC cases and unaffected controls. We observed that increased dietary intake of total fat, saturated fat, cholesterol, and red meat was significantly associated with CRC. Among non-ApoE4 carriers, 2-4 and 44 red meat servings/week were associated with developing MSS/L CRC (OR 1.51, 95% CI 1.10-2.07 and OR 1.80, 95% CI 1.30-2.48, respectively), whereas among ApoE4 allele carriers, four or more red meat servings/week were associated with MSI-H CRC (OR 4.62, 95% CI 1.20-17.77) when compared with the controls. ApoE isoforms modulate the risk of MSI-H and MSS/L CRCs among high red meat consumers. British Journal of Cancer (2009) 100, 1966-1974. doi: 10.1038/sj.bjc.6605097 www.bjcancer.com Published online 19 May 2009 (C) 2009 Cancer Research UK

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