Literature DB >> 24743756

A novel parameter, cell-cycle progression index, for radiation dose absorbed estimation in the premature chromosome condensation assay.

Tomisato Miura1, Akifumi Nakata2, Kosuke Kasai3, Manabu Nakano3, Yu Abe4, Eiki Tsushima5, Natalia I Ossetrova6, Mitsuaki A Yoshida2, William F Blakely6.   

Abstract

The calyculin A-induced premature chromosome condensation (PCC) assay is a simple and useful method for assessing the cell-cycle distribution in cells, since calyculin A induces chromosome condensation in various phases of the cell cycle. In this study, a novel parameter, the cell-cycle progression index (CPI), in the PCC assay was validated as a novel biomarker for biodosimetry. Peripheral blood was drawn from healthy donors after informed consent was obtained. CPI was investigated using a human peripheral blood lymphocyte (PBL) ex vivo irradiation ((60)Co-gamma rays: ∼0.6 Gy min(-1), or X ray: 1.0 Gy min(-1); 0-10 Gy) model. The calyculin A-induced PCC assay was performed for chromosome preparation. PCC cells were divided into the following five categories according to cell-cycle stage: non-PCC, G1-PCC, S-PCC, G2/M-PCC and M/A-PCC cells. CPI was calculated as the ratio of G2/M-PCC cells to G1-PCC cells. The PCC-stage distribution varied markedly with irradiation doses. The G1-PCC cell fraction was significantly reduced, and the G2/M-PCC cell fraction increased, in 10-Gy-irradiated PBL after 48 h of culture. CPI levels were fitted to an exponential dose-response curve with gamma-ray irradiation [y = 0.6729 + 0.3934 exp(0.5685D), r = 1.0000, p < 0.0001] and X-ray irradiation [y = -0.3743 + 0.9744 exp(0.3321D), r = 0.9999, p < 0.0001]. There were no significant individual (p = 0.853) or gender effects (p = 0.951) on the CPI in the human peripheral blood ex vivo irradiation model. Furthermore, CPI measurements are rapid (< 15 min per case). These results suggest that the CPI is a useful screening tool for the assessment of radiation doses received ranging from 0 to 10 Gy in radiation exposure early after a radiation event, especially after a mass-casualty radiological incident. Published by Oxford University Press 2014. This work is written by (a) US Government employee(s) and is in the public domain in the US.

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Year:  2014        PMID: 24743756     DOI: 10.1093/rpd/ncu126

Source DB:  PubMed          Journal:  Radiat Prot Dosimetry        ISSN: 0144-8420            Impact factor:   0.972


  3 in total

1.  Identification and Preliminary Validation of Radiation Response Protein(s) in Human Blood for a High-throughput Molecular Biodosimetry Technology for the Future.

Authors:  Saibadaiahun Nongrum; S Thangminlal Vaiphei; Joshua Keppen; Mandahakani Ksoo; Ettrika Kashyap; Rajesh N Sharan
Journal:  Genome Integr       Date:  2017-01-23

2.  Standardization of CalyculinA induced PCC assay and its advantages over Okadaic acid PCC assay in Biodosimetry applications.

Authors:  Rajesha K Nairy; Narayana Yerol; Nagesh N Bhat; Utkarsha Desai; Kapil Shirsath; Usha Yadav; Rajesh K Chaurasia; Sapra B K
Journal:  J Occup Health       Date:  2016-10-07       Impact factor: 2.708

3.  Investigation of DNA Damage and Cell-Cycle Distribution in Human Peripheral Blood Lymphocytes under Exposure to High Doses of Proton Radiotherapy.

Authors:  Justyna Miszczyk
Journal:  Biology (Basel)       Date:  2021-02-03
  3 in total

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