Methylmercury exposure, mercury metabolism genotypes, and risk of adult glioma
Methylmercury exposure, mercury metabolism genotypes, and risk of adult glioma
批准号:
8582978
负责人:
Kathleen M. Egan
金额:
$8.43万
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-07-03 至 2015-06-30
关键词:
ABCC1 geneAccountingAdultAdult GliomaAdverse effectsAntioxidantsAstrocytesBlood - brain barrier anatomyBrainCase-Control StudiesCellsCentral Nervous System NeoplasmsChildClipCommunitiesConsumptionDNADevelopmentDietary AssessmentEnvironmental PollutionEnvironmental Risk FactorEnzymesEtiologyEvaluationExcess MortalityFishesFundingFutureGCLC geneGCLM geneGenesGenetic PolymorphismGenetic Predisposition to DiseaseGenetic RiskGenetic VariationGenotypeGlioblastomaGliomaGlutathioneGrantHumanIndividual DifferencesInvestigationMMP2 geneMalignant NeoplasmsMalignant neoplasm of brainMeasurementMeasuresMediatingMedical centerMercuryMetabolic BiotransformationMetabolismMethylmercury CompoundsNail plateNervous System PhysiologyNeuraxisNeurotoxinsOralOutcomeOxidative StressParticipantPathway interactionsPatientsPopulation StudyReactive Oxygen SpeciesResourcesRiskRisk FactorsSamplingSeleniumShellfishSingle Nucleotide PolymorphismSourceStructure of nail of toeToxic effectTrace ElementsVariantabstractingbasecancer epidemiologymethylmercury exposuremortalityprenatal exposureprogramspublic health relevancerelating to nervous systemresponseselenoproteintumoruptake
中文摘要
描述(申请人提供):胶质瘤是一种病因不明的高致命性恶性肿瘤,占成人恶性脑肿瘤的近80%。该项目的目的是对甲基汞(MeHg)暴露与胶质瘤风险和存活率的关系进行探索性调查。甲基汞是一种强有力的神经毒素,对产前接触的成年人和儿童的神经功能都有不良影响。甲基汞是一种无处不在的环境污染物,食用鱼类和贝类是接触的主要来源。中枢神经系统对甲基汞的毒性非常敏感,因为这种化合物能够穿过血脑屏障,积聚在神经星形胶质细胞中,而神经星形胶质细胞是大脑中导致胶质瘤的细胞。甲基汞被认为会触发活性氧物种的过量产生,导致氧化应激和随后的细胞损伤。也有证据表明,甲基汞抑制了谷胱甘肽和硒蛋白的抗氧化作用,这两种酶介导了硒的大部分抗氧化功能。该项目将基于NCI资助的多中心(R01 CA116174)病例对照研究,探索美国东南部主要医疗中心正在进行的成人胶质瘤的遗传和环境风险因素。所有研究参与者都可以获得用来测量微量元素水平的指甲剪片和用来研究遗传易感性的口腔DNA样本。鉴于鱼类中甲基汞含量的高度变异性和汞代谢的个体差异,测量指甲剪下的甲基汞水平将比饮食评估提供更准确的甲基汞暴露测量。该项目的具体目标是:1)检测250例脑胶质瘤发病病例和250名匹配的社区对照人群的趾甲甲基汞;2)1200例病例和1200名对照人群的趾甲甲基汞基因功能或标记单核苷酸多态,这些基因涉及甲基汞的运输(SLC7A8、SLC7A5、SLC11A2)、生物转化(GCLC、GCLM)、分布(MT1A、MT1M、MT2A、MT4、MTF1)和消除(MRP1、MRP2);以及3)评估趾甲甲基汞和汞代谢基因与脑胶质瘤风险和患者预后的关系。据我们所知,这将是第一项人群研究,调查甲基汞暴露作为潜在的胶质瘤危险因素,并评估汞代谢的遗传变异与胶质瘤。基于一项大型的、即将完成的病例对照研究,拟议的先导性研究可能会为潜在的环境风险因素、胶质瘤肿瘤发展的机制以及未来研究方向提供新的信息。
英文摘要
DESCRIPTION (provided by applicant): Abstract Glioma is a highly lethal malignancy with unknown etiology that accounts for nearly 80% of adult malignant brain tumors. The aims of this project are to conduct an exploratory investigation of the relationship of methylmercury (MeHg) exposure with glioma risk and survival. MeHg is a potent neurotoxin associated with adverse effects on neurologic function both in adults and in children exposed prenatally. MeHg is a ubiquitous environmental contaminant with fish and shellfish consumption comprising the major source of exposure. The central nervous system is highly susceptible to the toxic effects of MeHg since the compound is able to cross the blood-brain barrier and accumulates in neural astrocytes, the cells in the brain which give rise to glioma. MeHg has been suggested to trigger the overproduction of reactive oxygen species causing oxidative stress and subsequent cellular damage. There is also evidence that MeHg inhibits the antioxidant effects of glutathione and selenoproteins, enzymes which mediate most of the antioxidant functions of selenium. The project will be based on a multicenter NCI-funded (R01 CA116174) case-control study exploring genetic and environmental risk factors for adult glioma underway at major medical centers in the Southeastern US. Nail clippings to measure levels of trace elements and oral DNA samples to study genetic susceptibility are available for all study participants. Given the high variability o MeHg content in fish and individual differences in mercury metabolism, measuring MeHg levels in nail clippings will provide a more accurate measurement of MeHg exposure than dietary assessment. Specific aims of this project are to: 1) Measure toenail MeHg in 250 incident glioma cases and 250 matched community controls; 2) Genotype functional or tagging single nucleotide polymorphisms in 1200 cases and 1200 controls for genes involved in the transport (SLC7A8, SLC7A5, SLC11A2), biotransformation (GCLC, GCLM), distribution (MT1A, MT1M, MT2A, MT4, MTF1), and elimination (MRP1, MRP2) of MeHg; and 3) Evaluate associations of toenail MeHg and mercury metabolism genotypes with glioma risk and patient outcome. To our knowledge this will be the first population study to investigate MeHg exposure as a potential glioma risk factor and to evaluate genetic variation in mercury metabolism with glioma. Based on a large, nearly completed case-control study, the proposed pilot investigation may provide new information on a potential environmental risk factor, mechanisms for glioma tumor development, and directions for future study.
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