) The overall research objectives of this program project are directed toward understanding the mechanistic bases for the recognition, processing and consequences of radiation induced lesions, with a particular emphasis on radon progeny alpha particles and their impact on human health. Nuclear DNA changes significantly impact human health with clear relationships to cell death, mutation and oncogenic changes. There is uncertainty however as to the potential contributions of stresses induced in non-nuclear targets to long term deleterious effects. It is clear that molecular interplay between membrane, cytoplasm and nucleus contributes to damage recognition, signaling and response pathways. An understanding of the role of cellular components in radiation responses can efficiently be obtained by use of a microbeam. In this project we will used defined influences (down to 1) or 100 keV/um alpha-particles to irradiate cell nucleus, cytoplasm or known cells in a population. Non-hit cells (bystanders) may be stressed by reactive oxygen species and/or affected by induced mobile cytokines. Mouse embryo fibroblasts derived from knockout mice, wild-type, p53-, and atm- will be irradiated both as single and as pair wise populations. Responses will be separately assessed in hit versus non-hit cells. We will ask the questions: Does particle spacing influence nucleus based responses? Does cytoplasmic irradiation initiate a biological response? Does cell specific irradiation initiate responses in non-hit cells on a genotype dependent basis? We will examine incidence of micronuclei; apoptosis, cell growth and development; cell cycle delay; and gene expression both by protein expression and localization, and mRNA by RT-PCR. In concert with the other projects of this program project, the combination of endpoints and precise site specific microbeam irradiation to address definitive question will establish mechanistic parameters and will define alpha-particle responsiveness at low doses with emphasis on the contribution of the bystander effect.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
2P01CA049062-10
Application #
6300351
Study Section
Project Start
2000-04-01
Project End
2001-03-31
Budget Start
Budget End
Support Year
10
Fiscal Year
2000
Total Cost
$243,335
Indirect Cost
Name
Columbia University (N.Y.)
Department
Type
DUNS #
167204994
City
New York
State
NY
Country
United States
Zip Code
10032
Wu, Jinhua; Hei, Tom K (2018) Focus small to find big - the microbeam story. Int J Radiat Biol 94:782-788
Liao, Wupeng; Hei, Tom K; Cheng, Simon K (2017) Radiation-Induced Dermatitis is Mediated by IL17-Expressing ?? T Cells. Radiat Res 187:454-464
Wu, Jinhua; Zhang, Bo; Wuu, Yen-Ruh et al. (2017) Targeted cytoplasmic irradiation and autophagy. Mutat Res 806:88-97
Wu, Jinhua; Zhang, Qin; Wuu, Yen-Ruh et al. (2017) Cytoplasmic Irradiation Induces Metabolic Shift in Human Small Airway Epithelial Cells via Activation of Pim-1 Kinase. Radiat Res 187:441-453
Domogauer, Jason D; de Toledo, Sonia M; Azzam, Edouard I (2016) A Mimic of the Tumor Microenvironment: A Simple Method for Generating Enriched Cell Populations and Investigating Intercellular Communication. J Vis Exp :
Chen, Hongxin; Chong, Zhao Zhong; De Toledo, Sonia M et al. (2016) Delayed activation of human microglial cells by high dose ionizing radiation. Brain Res 1646:193-198
Azzam, Edouard I; Colangelo, Nicholas W; Domogauer, Jason D et al. (2016) Is Ionizing Radiation Harmful at any Exposure? An Echo That Continues to Vibrate. Health Phys 110:249-51
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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