This Program Project presents, brings together, and links five projects designed to investigate the biological effects of alpha particles with LETs simulating those emitted by the daughter products of radon. The individual projects each address this central theme from different points of view. The earliest observable biological effect of radiation in individual cells is the production of chromosome aberrations, and their production by alpha particles will be studied in detail. The special feature of this project is the attempt to quantitate the effect of precisely known numbers of alpha particles traversing single cells. This is particularly important, as it is likely that most cells at risk will be traversed by no more than one alpha particle. Since the hazard of radon in the human involves the stochastic late effects of carcinogenesis, the experimental studies focus directly on oncogenic transformation and on mutations or DNA modulations, which may be early steps involved in the carcinogenic process. A variety of cellular and molecular studies are proposed in this area. Assays for oncogenic transformation represent a powerful tool and will be used for pragmatic studies involving the possible supra-additive interaction of alpha particles with asbestos, tobacco-smoke condensate, and a variety of chemicals, as well as the study of modulating influences, such as hormones and retinoids. Mechanistic studies will be designed to identify and characterize the molecular changes that lead to the induction of malignancy. The alpha particles emitted by the radon daughters cover a range of energies, and by the time they reach the critical cells in the lung, they have LET values from about 90 to 250 keV/(mu)m. Alpha particles with this range of LET values will be generated at the Radiological Research Accelerator Facility.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA049062-05
Application #
2093160
Study Section
Special Emphasis Panel (SRC (I3))
Project Start
1990-05-15
Project End
1995-03-31
Budget Start
1994-04-01
Budget End
1995-03-31
Support Year
5
Fiscal Year
1994
Total Cost
Indirect Cost
Name
Columbia University (N.Y.)
Department
Radiation-Diagnostic/Oncology
Type
Schools of Medicine
DUNS #
064931884
City
New York
State
NY
Country
United States
Zip Code
10027
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Liao, Wupeng; Hei, Tom K; Cheng, Simon K (2017) Radiation-Induced Dermatitis is Mediated by IL17-Expressing ?? T Cells. Radiat Res 187:454-464
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Hei, Tom K (2016) Response of Biological Systems to Low Doses of Ionizing Radiation. Health Phys 110:281-2
Gong, Xuezhong; Ivanov, Vladimir N; Hei, Tom K (2016) 2,3,5,6-Tetramethylpyrazine (TMP) down-regulated arsenic-induced heme oxygenase-1 and ARS2 expression by inhibiting Nrf2, NF-?B, AP-1 and MAPK pathways in human proximal tubular cells. Arch Toxicol 90:2187-2200
Ivanov, Vladimir N; Hei, Tom K (2015) Regulation of viability, differentiation and death of human melanoma cells carrying neural stem cell biomarkers: a possibility for neural trans-differentiation. Apoptosis 20:996-1015

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