期刊文献+

化学物暴露与白血病发病相关基因DNA甲基化对儿童急性白血病发病的影响 被引量:6

Chemical exposure, leukemia related DNA methylation changes and childhood acute leukemia
原文传递
导出
摘要 目的:探讨化学物暴露、白血病发病相关DNA甲基化改变以及二者交互作用与儿童急性白血病发病的关系。方法2009年1月1日至2010年12月31日,采用1∶1匹配的病例-对照研究方法,选取131例就诊于3家上海市三甲级儿童医院的0~15岁新发急性白血病患儿为病例组,选取病例所在医院的发育行为儿科或骨科门诊就诊或入院治疗与病例组同性别、同年龄的儿童为对照组,排除患血液系统疾病、肿瘤疾病等的儿童。对两组儿童进行相关环境因素的问卷调查,采用甲基化特异性聚合酶链反应(MSP)分析病例组与对照组儿童8个与白血病发病相关的基因(P16、P73、E-cadherin、DAPK、C-ABL、HSPA4L、PTEN、APAF-1)的甲基化状态,并分析环境暴露因素与基因甲基化水平改变之间的交互作用,以相对超额危险度(RERI)、归因比(API)与交互作用指数(S)描述其交互作用。结果病例组和对照组分别为131和140例,年龄分别为(6.9±3.8)和(6.9±3.9)岁(t=0.01,P=0.911)。将混杂因素校正后,儿童期(OR=3.90,95%CI:1.69~9.02)、母亲孕前及孕期(OR=2.71,95%CI:1.12~6.52)、父亲在母亲怀孕前(OR=1.91,95%CI:1.05~3.47)接触化学物与儿童急性白血病发生相关。病例组儿童DAPK、PTEN、P73基因甲基化程度高于对照组儿童[病例组分别为:3.1%(4例),16.0%(21例),7.6%(10例);对照组分别为:0.7%(1例),2.9%(4例),0.7%(1例),χ2值分别为7.11、16.90、11.38,P值分别为0.029、0.000、0.003],但病例组P16基因的甲基化程度低于对照组儿童[病例组比对照组:3.8%(5例)比8.6%(12例),χ2=10.33, P=0.007]。环境-基因交互作用结果显示,儿童化学物质接触史与PTEN、P16、P73等3种基因存在交互作用(PTEN:RERI=-7.01,API=-2.14,S=0.24;P16:RERI=4.08,API=0.53,S=2.59;P73:RERI=4.32,API=0.48,S=2.19);母亲� Objective To evaluate the association between chemical exposure, DNA methylation status and gene-environment interactions in the development of childhood acute leukemia (AL). Methods From January 1st 2009 to December 31st 2010,an exploratory case-control study was conducted on childhood AL among children who were less than 15 years of age in Shanghai, China. A total of 131 patients with newly diagnosed AL were recruited from 3 Shanghai children hospitals. The controls selected from the same hospital were healthy children who attended the physical check-up held by the department of Children's Healthcare, or who visited the clinic of developmental pediatrics or orthopedics (excluding blood 〈br〉 diseases and malignant tumors). 140 controls matched with cases in gender and age were included in this study. Chemical exposure were investigated by questionnaires, methylation specific polymerase chain reaction (MSP) was adopted to analyze the methylation or deletion status of 8 genes, and gene-environment interactions were analyzed by relative excess risk of interaction (RERI), attributable proportion of interaction (API) and synergy index (S). Results There were 131 and 140 subjects in case and control group,who were aged(6.9 ± 3.8)and(6.9 ± 3.9)years old(t=0.01,P=0.911),respectively. After adjusting age and other potential confounding factors, chemical substances' exposure of children/mother/father were all significantly higher in cases than that in controls (Children: OR=3.90, 95%CI:1.69-9.02; Mother: OR=2.71, 95%CI:1.12-6.52;Father:OR=1.91, 95%CI:1.05-3.47). For the 8 genes analyzed, the methylation status of DAPK and PTEN and P73 in case group were significantly higher than that in control group (cases:3.1%(4 cases), 16.0%(21 cases),7.6%(10 cases);controls:0.7%(1 case),2.9%(4 cases),0.7%(1 case);χ2:7.11,16.90,11.38;P value:0.029, 0.000, 0.003). The methylation status of P16 in case group was significantly lower than tha
出处 《中华预防医学杂志》 CAS CSCD 北大核心 2015年第9期800-809,共10页 Chinese Journal of Preventive Medicine
基金 国家自然科学基金(30901171) 上海市自然科学基金(09ZR1416500、12ZR1416100) 上海市公共卫生重点学科建设计划(12GWZX0401) 上海交通大学医学院科技基金(12XJ10006、12XJ10042、12XJ10043)
关键词 白血病 双表型 急性 儿童 DNA甲基化 环境 基因-环境交互作用 Leukemia,biphenotypic,acute Child DNA methylation Environment Gene-environment-interaction
  • 相关文献

参考文献26

  • 1Canadian Cancer Society,National Cancer Institute of Canada. Canadian cancer statistics 2009[M]. Toronto: Canadian Cancer Society,2009. 被引量:1
  • 2Barr DB, Bravo R, Weerasekera G, et al. Concentration of dialkyl phosphate metabolites of organophosphorus pesticides in the U.S. population[J]. Environ Health Perspect,2004,112(2) : 186-200. 被引量:1
  • 3Turner MC, Wigle DT, Krewski D. Residential pesticides and childhood leukemia: a systematic review and meta-analysis[J]. Environ Health Perspect, 2010, 118(1): 33-41. 被引量:1
  • 4Eden T. Aetiology of childhood leukaemia[J]. Cancer Treat Rev,2010,36: 286-297. 被引量:1
  • 5Garcia-Manero G, Yang H, Kuang SQ, et al. Epigeneties of acute lymphocytic leukemia[J]. Semin Hematol, 2009,46(1): 24-32. 被引量:1
  • 6Lightfoot T, Roman E. Causes of childhood leukaemia and lymphoma[J]. Toxical Appl Pharmacol, 2004,199 : 104-117. 被引量:1
  • 7Kim AS, Eastmond DA, Preston RJ. Childhood acute lymphocytic leukemia and perspectives on risk assessment of early-life stage exposures[J]. Mutat Res, 2006, 613(2/3): 138-160. 被引量:1
  • 8Trevino LR, Yang W, French D, et al. Germline genomic variants associated with childhood acute lymphoblastic leukemia[J]. Nat Genet, 2009,41 (9) : 1001-1005. 被引量:1
  • 9Sherborne AL, Hosking FJ, Prasad RB, et al. Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk[J]. Nat Genet, 2010, 42(6): 492-494. 被引量:1
  • 10Roman-Gomez J, Jimenez-Velasco A, Castillejo JA, et al. Promoter hypermethylation of cancer-related genes: a strong independent prognostic factor in acute lymphoblastic leukemia[J]. Blood, 2004,104: 2492-2498. 被引量:1

二级参考文献68

共引文献20

同被引文献45

引证文献6

二级引证文献16

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部