The goal of this project is to further understanding of how short-lived reactive oxidizing species (ROS) generated outside the nucleus nevertheless lead to the induction of gene locus mutations. To accomplish this, this project will investigate quantitative and qualitative aspects of the induction of gene mutations by ROS generated outside the nucleus, and compare them to mutations generated by ROS within the nucleus. ROS will be produced uniformly within the cell or targeted to non-nuclear regions by using photo-activated dyes that concentrate in specific sub-cellular compartments. Quantitative and qualitative measurements of DNA damage will be made using the comet, or single ceil gel electrophoresis assay. The mutagenicity studies will involve a two-pronged approach. First, quantitative dose-response experiments will be carried out at two endogenous gene loci, and measured as a function of damage to DNA. Second, the qualitative natures of induced mutants will be determined by analyses of mutational spectra induced by the various treatments. These studies will be done initially in human lymphoblastoid cells with a mutated p53 gene. An additional set of experiments will address the question of whether mutagenic effects of ROS exposure are dependent on p53 status. The same strategies described above will be repeated using p53 wild type and null cells from the same donor. Finally, another set of experiments will examine effects of the Fanconi's anemia complex on ROS mutagenesis.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA095227-03
Application #
7268861
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
Budget Start
2006-08-01
Budget End
2007-07-31
Support Year
3
Fiscal Year
2006
Total Cost
$232,555
Indirect Cost
Name
Massachusetts General Hospital
Department
Type
DUNS #
073130411
City
Boston
State
MA
Country
United States
Zip Code
02199
Prise, K M; Schettino, G (2011) Microbeams in radiation biology: review and critical comparison. Radiat Prot Dosimetry 143:335-9
Purschke, Martin; Rubio, Noemi; Held, Kathryn D et al. (2010) Phototoxicity of Hoechst 33342 in time-lapse fluorescence microscopy. Photochem Photobiol Sci 9:1634-9
Schettino, Giuseppe; Al Rashid, Shahnaz T; Prise, Kevin M (2010) Radiation microbeams as spatial and temporal probes of subcellular and tissue response. Mutat Res 704:68-77
Prise, Kevin M; Schettino, Giuseppe; Vojnovic, Boris et al. (2009) Microbeam studies of the bystander response. J Radiat Res 50 Suppl A:A1-6
Rubio, Noemi; Fleury, Sean P; Redmond, Robert W (2009) Spatial and temporal dynamics of in vitro photodynamic cell killing: extracellular hydrogen peroxide mediates neighbouring cell death. Photochem Photobiol Sci 8:457-64
Zhang, Ying; Zhou, Junqing; Baldwin, Joseph et al. (2009) Ionizing radiation-induced bystander mutagenesis and adaptation: quantitative and temporal aspects. Mutat Res 671:20-5
Prise, Kevin M; O'Sullivan, Joe M (2009) Radiation-induced bystander signalling in cancer therapy. Nat Rev Cancer 9:351-60
Burdak-Rothkamm, Susanne; Prise, Kevin M (2009) New molecular targets in radiotherapy: DNA damage signalling and repair in targeted and non-targeted cells. Eur J Pharmacol 625:151-5
Rubio, Noemi; Rajadurai, Anpuchchelvi; Held, Kathryn D et al. (2009) Real-time imaging of novel spatial and temporal responses to photodynamic stress. Free Radic Biol Med 47:283-90
Chakraborty, Asima; Held, Kathryn D; Prise, Kevin M et al. (2009) Bystander effects induced by diffusing mediators after photodynamic stress. Radiat Res 172:74-81

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