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本文引用的文献

1
Hypermethylator phenotype in sporadic colon cancer: study on a population-based series of 582 cases.散发性结肠癌中的高甲基化表型:基于582例人群系列研究
Cancer Res. 2008 Oct 15;68(20):8541-6. doi: 10.1158/0008-5472.CAN-08-1171.
2
Intra-individual change over time in DNA methylation with familial clustering.DNA甲基化随时间的个体内变化与家族聚集性。
JAMA. 2008 Jun 25;299(24):2877-83. doi: 10.1001/jama.299.24.2877.
3
Genetic and epigenetic changes in colon cancer.结肠癌中的基因和表观遗传变化。
Exp Mol Pathol. 2008 Aug;85(1):64-7. doi: 10.1016/j.yexmp.2008.03.008. Epub 2008 Apr 8.
4
Epigenetic drivers and genetic passengers on the road to cancer.癌症发展过程中的表观遗传驱动因素和基因乘客因素
Mutat Res. 2008 Jul 3;642(1-2):1-13. doi: 10.1016/j.mrfmmm.2008.03.002. Epub 2008 Mar 25.
5
Systemic folate status and risk of colorectal cancer.
Cancer Causes Control. 2008 Nov;19(9):1005-7; author reply 1003. doi: 10.1007/s10552-008-9161-6. Epub 2008 Apr 26.
6
Mutations in both KRAS and BRAF may contribute to the methylator phenotype in colon cancer.KRAS和BRAF基因的突变可能都与结肠癌的甲基化表型有关。
Gastroenterology. 2008 Jun;134(7):1950-60, 1960.e1. doi: 10.1053/j.gastro.2008.02.094. Epub 2008 Mar 8.
7
LINE-1 hypomethylation is inversely associated with microsatellite instability and CpG island methylator phenotype in colorectal cancer.LINE-1低甲基化与结直肠癌中的微卫星不稳定性和CpG岛甲基化表型呈负相关。
Int J Cancer. 2008 Jun 15;122(12):2767-73. doi: 10.1002/ijc.23470.
8
Epigenetics at the epicenter of modern medicine.表观遗传学处于现代医学的核心位置。
JAMA. 2008 Mar 19;299(11):1345-50. doi: 10.1001/jama.299.11.1345.
9
Epigenetics in cancer.癌症中的表观遗传学
N Engl J Med. 2008 Mar 13;358(11):1148-59. doi: 10.1056/NEJMra072067.
10
Pharmacological inhibition of DNA methylation induces proinvasive and prometastatic genes in vitro and in vivo.DNA甲基化的药理学抑制在体外和体内均可诱导促侵袭和促转移基因。
Neoplasia. 2008 Mar;10(3):266-78. doi: 10.1593/neo.07947.

一条碳代谢途径中的种系多态性与结直肠癌中的 DNA 甲基化。

Germline polymorphisms in the one-carbon metabolism pathway and DNA methylation in colorectal cancer.

机构信息

Department of Epidemiology, Harvard School of Public Health, Boston, MA 02115, USA.

出版信息

Cancer Causes Control. 2010 Mar;21(3):331-45. doi: 10.1007/s10552-009-9464-2.

DOI:10.1007/s10552-009-9464-2
PMID:19936946
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3570978/
Abstract

Dietary intake of one-carbon nutrients (methyl donors) and germline variants in the one-carbon metabolism genes may influence global DNA methylation level and methylation in promoter CpG islands. In this study, we evaluated the relationship between single nucleotide polymorphisms (SNPs) in the one-carbon metabolism pathway and DNA methylation status in colorectal cancer. Utilizing 182 colorectal cancers cases in two prospective cohort studies, we determined the CpG island methylator phenotype (CIMP) status on eight CIMP-specific promoters and measured LINE-1 methylation level that correlates well with genome-wide DNA methylation level. We genotyped 23 nonsynonymous SNPs in the one-carbon metabolism genes using buffy coat DNA. Most of the 23 SNPs in the one-carbon metabolism pathway were not significantly associated with CIMP-high status (> or = 6/8 methylated promoters). However, the MTHFR 429 Ala/Ala variant (rs1801131) and the TCN2 259 Arg/Arg variant (rs1801198) were associated with CIMP-high status (MTHFR 429 multivariate odds ratio (MV OR) = 7.56; 95% confidence interval (CI), 1.32-43.3; p trend = 0.10; TCN2 259 Arg/Arg variant MV OR = 3.82; 95% CI, 1.02-14.4; p trend = 0.06). The one-carbon metabolism genotypes were not significantly associated with LINE-1 methylation, although there were modest differences in mean LINE-1 methylation levels between certain genotypes. Collectively, these exploratory data provide suggestive evidence for the association of MTHFR 429 Ala/ Ala and TCN2 259 Arg/Arg and CIMP status in colorectal cancer.

摘要

饮食中单碳营养素(甲基供体)的摄入量和单碳代谢基因中的种系变异可能会影响全球 DNA 甲基化水平和启动子 CpG 岛的甲基化。在这项研究中,我们评估了单碳代谢途径中的单核苷酸多态性(SNP)与结直肠癌中 DNA 甲基化状态之间的关系。我们利用两项前瞻性队列研究中的 182 例结直肠癌病例,确定了八个 CIMP 特异性启动子上的 CpG 岛甲基化表型(CIMP)状态,并测量了与全基因组 DNA 甲基化水平密切相关的 LINE-1 甲基化水平。我们使用血斑 DNA 对单碳代谢基因中的 23 个非同义 SNP 进行了基因分型。单碳代谢途径中的 23 个 SNP 大多数与 CIMP-高状态(≥6/8 个甲基化启动子)无显著相关性。然而,MTHFR 429 Ala/Ala 变体(rs1801131)和 TCN2 259 Arg/Arg 变体(rs1801198)与 CIMP-高状态相关(MTHFR 429 多变量优势比(MV OR)=7.56;95%置信区间(CI),1.32-43.3;p 趋势=0.10;TCN2 259 Arg/Arg 变体 MV OR=3.82;95%CI,1.02-14.4;p 趋势=0.06)。尽管某些基因型之间存在平均 LINE-1 甲基化水平的适度差异,但单碳代谢基因型与 LINE-1 甲基化无显著相关性。总的来说,这些探索性数据为 MTHFR 429 Ala/Ala 和 TCN2 259 Arg/Arg 与结直肠癌中的 CIMP 状态之间的关联提供了提示性证据。