Literature DB >> 8609451

Comparison of chromosomal damage induced by X-rays and Ar ions with an LET of 1840 keV/micrometer in G1 V79 cells.

S Ritter1, E Nasonova, M Scholz, W Kraft-Weyrather, G Kraft.   

Abstract

Synchronous V79 Chinese hamster cells were exposed in G1 to either X-rays or 4.6 MeV/u Ar-ions (LET = 1840 keV/micrometer) and the induction of chromosomal damage was measured at five sampling times ranging from 14 to 30 h after treatment. To distinguish between cells in the first and second post-irradiation cycle the fluorescence-plus-Giemsa technique was applied. The experiment showed that the time-course of the appearance of damaged cells was markedly influenced by radiation-induced cell cycle delays and depended on both radiation quality and dose. The yield of aberrant metaphases and the number of aberrations per metaphase was found to increase with sampling time, but this increase was more pronounced for Ar ions. These differences in yield-time profiles of X-ray and Ar ion induced chromosomal damage are particularly important for an accurate determination of the RBE for particles. Our data clearly indicate that meaningful RBEs can only be obtained if chromosomal damage is analysed at several post-irradiation sampling times and the complete time-course of the expression of chromosomal damage is taken into account. Besides these quantitative differences, differences in the spectrum of chromosomal lesions were observed for X-rays and Ar ions. Following particle exposure more breaks and less exchange-type aberrations were formed compared with X-irradiation and, despite irradiation in G(1), a significant number of chromatid-type aberrations occurred in Ar-irradiated samples. The experimental results are interpreted on the basis of the different pattern of energy deposition by sparsely and densely ionizing radiation. In addition, a statistical analysis based on the Neyman type A distribution is performed, which takes into account the specific stochastic properties of particle irradiation.

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Year:  1996        PMID: 8609451     DOI: 10.1080/095530096145986

Source DB:  PubMed          Journal:  Int J Radiat Biol        ISSN: 0955-3002            Impact factor:   2.694


  7 in total

1.  Influence of mitotic delay on the results of biological dosimetry for high doses of ionizing radiation.

Authors:  A Heimers; H J Brede; U Giesen; W Hoffmann
Journal:  Radiat Environ Biophys       Date:  2005-11-05       Impact factor: 1.925

2.  Biodosimetry estimate for high-LET irradiation.

Authors:  Z Z Wang; W J Li; D J Zhi; X G Jing; W Wei; Q X Gao; B Liu
Journal:  Radiat Environ Biophys       Date:  2007-04-19       Impact factor: 1.925

3.  Chromosome aberration measurements in mitotic and G2-PCC lymphocytes at the standard sampling time of 48 h underestimate the effectiveness of high-LET particles.

Authors:  Ryonfa Lee; Elena Nasonova; Carola Hartel; Marco Durante; Sylvia Ritter
Journal:  Radiat Environ Biophys       Date:  2011-04-11       Impact factor: 1.925

4.  Modeling radiation-induced cell cycle delays.

Authors:  Anna Ochab-Marcinek; Ewa Gudowska-Nowak; Elena Nasonova; Sylvia Ritter
Journal:  Radiat Environ Biophys       Date:  2009-08-11       Impact factor: 1.925

5.  Chromosome damage in human cells by γ rays, α particles and heavy ions: track interactions in basic dose-response relationships.

Authors:  Bradford D Loucas; Marco Durante; Susan M Bailey; Michael N Cornforth
Journal:  Radiat Res       Date:  2012-11-30       Impact factor: 2.841

6.  Latexin sensitizes leukemogenic cells to gamma-irradiation-induced cell-cycle arrest and cell death through Rps3 pathway.

Authors:  Y You; R Wen; R Pathak; A Li; W Li; D St Clair; M Hauer-Jensen; D Zhou; Y Liang
Journal:  Cell Death Dis       Date:  2014-10-23       Impact factor: 8.469

7.  Persistence of radiation-induced aberrations in patients after radiotherapy with C-ions and IMRT.

Authors:  Carola Hartel; Elena Nasonova; Martina C Fuss; Anna V Nikoghosyan; Juergen Debus; Sylvia Ritter
Journal:  Clin Transl Radiat Oncol       Date:  2018-10-10
  7 in total

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