% IMPORTANT: The following is UTF-8 encoded. This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.
@INPROCEEDINGS{Unverricht:838585,
author = {Unverricht, Marcus and Boldt and Giesen and Pomplun,
Ekkehard and Wolkenhauer and Kriehuber, Ralf},
title = {{WHOLE} {GENOME} {EXPRESSION} {ANALYSIS} {IN} {HUMAN}
{JURKAT} {CELLS} {AFTER} {EXPOSURE} {TO}
{I}-123-{IODODEOXYURIDINE}, γ-{RAYS} {AND} α-{PARTICLES}},
reportid = {FZJ-2017-07167},
year = {2011},
abstract = {Introduction: In order to develop a gene expression
profile-based method for biodosimetry purposes we used the
human p53-deficient T-lymphoma Jurkat cell line to study
whether gene signatures exist allowing the discrimination of
radiation quality as well.Methods: Equi-effect doses, i.e.
radiation doses and exposure conditions causing the same
biological effect level, were determined with regard to
micronucleus formation, γ-H2AX foci intensity and apoptosis
induction for the radiation qualities of γ-rays (Cs-137)
and α-particles (Am-241) as well as for the Auger electron
emitter I-123. Prior to the DNA-microarray based gene
expression experiments, Jurkat cells were either irradiated
with 0.8 and 5 Gy γ-rays, respectively with 0.1 and 0.5 Gy
α-particles or were exposed to 4 - 200 kBq
I-123-iododeoxyuridine (I-123-UdR) per 10E6 cells. I-123-UdR
was incorporated into the DNA of synchronized cells for 20
h. After quantification of the cellular uptake the
accumulated decays were calculated and the absorbed
radiation dose was assessed after 3-D geometry analysis of
the cells. RNA-isolation was performed always 6 h
post-exposure. Whole human genome DNA-microarrays (Agilent)
were processed and expression profiles were analyzed. Genes
showing significant expression changes after irradiation
were identified by one-way ANOVA and Tukey-HSD post-hoc
testing. The biological functions of significantly regulated
genes were further investigated.Results: Preliminary results
of the gene expression analysis after exposure to the three
investigated radiation qualities indicate that the
expression of more and different genes is significantly
altered after exposure to I-123-UdR when compared to γ- and
α-irradiation. The functional analysis of significantly
changed genes reveals that apoptosis relevant genes are
enriched after exposure to I-123-UdR in comparison to γ-
and α-irradiation. Conclusions: Changes in the gene
expression of p53-dependent apoptosis-related genes were
observed after I-123-UdR exposure suggesting p53-independent
back-up pathways for apoptosis signalling in Jurkat
cells.Funded by Kompetenzverbund Strahlenforschung (KVSF),
Bundesministerium für Bildung und Forschung (BMBF), Project
No.: 02NUK005A and 02NUK005D},
month = {Aug},
date = {2011-08-28},
organization = {14th International Congress of
Radiation Research, Warsaw (Poland), 28
Aug 2011 - 1 Sep 2011},
subtyp = {After Call},
cin = {S-US},
cid = {I:(DE-Juel1)S-US-20090406},
pnm = {899 - ohne Topic (POF3-899)},
pid = {G:(DE-HGF)POF3-899},
typ = {PUB:(DE-HGF)24},
url = {https://juser.fz-juelich.de/record/838585},
}