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Studies of Non-Ionizing Radiation-Related Cancer

Studies of Non-Ionizing Radiation-Related Cancer
非电离辐射相关癌症的研究
批准号:
10918973
负责人:
Elizabeth Cahoon
金额:
$42.88万
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:

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Case referent study of brain tumors - 04030 The etiology of brain tumors and brain cancer is poorly understood, and recorded incidence rates have increased dramatically over the past several decades. In response to these findings, and to advance understanding of environmental, behavioral and genetic causes of brain tumors, we conducted a case-control study of malignant and benign brain tumors (glioma, meningioma and acoustic neuroma). Excess risks of glioma were found among electricians and farmers, and an elevated risk of meningioma was seen among auto-body painters. Detailed occupational exposure assessments were conducted for electromagnetic radiation, lead, and pesticides. No associations were seen for electromagnetic radiation, but an association was suggested for meningioma and lead. No consistent evidence was found of an association between any of six chlorinated solvents and risk of glioma or meningioma although there was limited evidence of an association between carbon tetrachloride and risk of glioma. Recent genetic analyses have indicated associations between brain tumor risk and polymorphisms in cytokine, apoptosis/cell cycle control, DNA repair and oxidative stress genes. Findings for these pathways are being followed up in larger and more comprehensive studies. Cellular Telephone Use and Cancer Risks Ionizing radiation is known to increase cancer risks, but there is no consistent evidence that non-ionizing radiofrequency radiation (cell phones) or magnetic field (power lines and electrical appliances) exposures increase cancer risk. As a result of public and Congressional concern, the Radiation Epidemiology Branch (REB) launched an early case-control study and found no relationship between cell phone use and risk of glioma, meningioma or acoustic neuroma. A study of time trends in glioma incidence in the U.S. led by REB showed no rise despite dramatic increases in cell phone use. A subsequent REB assessment demonstrated that the elevated glioma risks associated with cell phone use in a Swedish study that influenced IARCs conclusion of possible carcinogenicity was not consistent with U.S. incidence trends, though incidence trends could be consistent with the small excess of glioma in the highest level users in the Interphone study. UV Dosimetry - 10262 A pilot study of 125 volunteer radiologic technologists was performed by REB investigators in which daily diaries and polysulfone UV dosimeters were used to develop better questionnaire approaches to ascertain environmental UV exposure for future studies of skin and other cancers in this largely female occupational population. The volunteers were queried 6 months later to test the reproducibility of responses to time outdoors. Agreement between reported time on weekdays was significantly higher than for weekends and the reproducibility of hour-based compared to activity-based questionnaires was poorer in adult women. Improved exposure assessment may enable us to characterize more quantitatively the effects of UV and ionizing radiation on skin and other cancers. PLCO Lung DNA Damage Study - 10334 It is unclear whether the reported associations between functional assays and increased lung cancer risk represent a true association because the tests were performed on biologic specimens collected after cancer diagnosis. It may be that they are measuring the consequence, rather than the underlying cause of cancer (termed reverse causation bias). Several DCEG investigators are participating in the effort to determine the predictive value of multiple phenotypic or functional assays in pre-diagnostic samples from lung cancer patients included in the Prostate, Lung, Colon, and Ovary (PLCO) screening trial. Primary study findings were that neomycin mutation sensitivity was associated with increased lung cancer risk. Further study of DNA repair genes will be done using existing GWAS data.
期刊论文(16)
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会议论文
DOI: 10.1158/1055-9965.epi-09-0197
发表时间: 2009-06
期刊: Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology
影响因子: --
作者: [Bhatti P, Stewart PA, Hutchinson A, Rothman N, Linet MS, Inskip PD, Rajaraman P]
通讯作者: Rajaraman P
DOI: 10.1016/j.jneuroim.2010.11.005
发表时间: 2011-04
期刊: JOURNAL OF NEUROIMMUNOLOGY
影响因子: 3.3
作者: [Bassig, Bryan A., Inskip, Peter D., Burdette, Laurie, Shapiro, William R., Selker, Robert G., Fine, Howard A., Loeffler, Jay S., Black, Peter M., Dubrow, Robert, Brenner, Alina V.]
通讯作者: Brenner, Alina V.
Prospective analysis of DNA damage and repair markers of lung cancer risk from the Prostate, Lung, Colorectal and Ovarian (PLCO) Cancer Screening Trial.
对前列腺癌、肺癌、结直肠癌和卵巢癌 (PLCO) 癌症筛查试验中肺癌风险的 DNA 损伤和修复标志物进行前瞻性分析。
DOI: 10.1093/carcin/bgq204
发表时间: 2011
期刊: Carcinogenesis
影响因子: 4.7
作者: [Sigurdson,AliceJ, Jones,IreneM, Wei,Qingyi, Wu,Xifeng, Spitz,MargaretR, Stram,DouglasA, Gross,MyronD, Huang,Wen-Yi, Wang,Li-E, Gu,Jian, Thomas,CynthiaB, Reding,DouglasJ, Hayes,RichardB, Caporaso,NeilE]
通讯作者: Caporaso,NeilE
DOI: 10.1158/1055-9965.epi-08-0894
发表时间: 2009-02
期刊: Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology
影响因子: --
作者: [Yu CL, Li Y, Freedman DM, Fears TR, Kwok R, Chodick G, Alexander B, Kimlin MG, Kricker A, Armstrong BK, Linet MS]
通讯作者: Linet MS
13
    Studies of Populations Exposed to Environmental Sources of Radiation
    Studies of Populations Exposed to Environmental Sources of Radiation
    Studies of Populations Exposed to Environmental Sources of Radiation
    Studies of Populations Exposed to Environmental Sources of Radiation
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