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Biological dosimetry is crucial for estimating the doses from biological samples and guiding medical interventions for accidental radiation exposure. This study aimed to derive rapid and precise dose estimates using a dicentric chromosome assay. To address the challenges of manual scoring of dicentric chromosomes, we upgraded an automatic system aimed at enhancing the precision of dicentric chromosome detection while reducing the need for human intervention. We collected blood from 30 individuals aged 20-67 years to create 30 dose-response curves aiming to investigate the differences in responses among individuals. To validate dose-estimate accuracy within a 95% confidence interval, blinded samples were categorized into three groups according to the radiation dose as follows: ≥2, ≤ 1, and 0.1 Gy. When scoring dicentric chromosomes without human review and constructing a dose-response curve, individual differences were observed. For doses ≤ 1 Gy, the standard root formula was effective; conversely, for doses ≥ 2 Gy, the regression deep neural network proved to be more ac-curate. Our developed program allowed for the rapid analysis of a large volume of dicentric chromosome images.
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http://dx.doi.org/10.1038/s41598-025-94678-8 | DOI Listing |
Methods Mol Biol
August 2025
Department of Hematology, Gustave Roussy Cancer Campus, Villejuif, France.
The analysis of the origin of chromothripsis, catastrophic chromosomal rearrangements, has provided exceptional insights into various aspects of tumor progression and genetic disorders. Findings in chromothripsis have not only enhanced our understanding of genomic instability mechanisms, but also reshaped our views on chromosome mechanics. To date, the major mechanisms of chromothripsis described involve the incorporation of micronuclei into the primary nucleus and telomere crisis through the formation of dicentric chromosomes.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
August 2025
Department of Microbiology and Molecular Genetics, University of California Davis, Davis, CA 95616.
DNA secondary G-quadruplex (G4) structures can impair and even obstruct DNA replication. Defects in processing G4 structures are associated with replication stress, a common property of both B cell cancers and hyperproliferative premalignant cells. Genome instability arising from replication stress is a hallmark of cancer and strongly contributes to the chromosome rearrangements in B cell cancers.
View Article and Find Full Text PDFBiol Methods Protoc
August 2025
Department of Radiobiology, Military Faculty of Medicine, University of Defence, Třebešská 1575, Hradec Králové, 500 02, Czech Republic.
The dicentric chromosome assay is a well-established biodosimetric method used to assess absorbed ionizing radiation doses by detecting dicentric chromosomal aberrations. Here, we present a detailed, reproducible protocol for applying the dicentric chromosome assay for evaluation of radioprotective agents, including novel piperazine derivatives compared with amifostine and its active metabolite WR-1065. The protocol covers all key steps-blood sample preparation, irradiation, lymphocyte culture, metaphase preparation, and scoring of dicentric chromosomes.
View Article and Find Full Text PDFSci Rep
August 2025
Radiological Physics and Advisory Division, Bhabha Atomic Research Centre (BARC), Mumbai, India.
This study investigated the long-term stability of cytogenetic and morphological markers, including dicentric chromosomes (DC), unbalanced translocation (UT), balanced translocation (BT), and Pseudo Pelger-Huët Anomaly (PPHA), in a radiation worker exposed to an acute dose of Co-γ radiation. Initial dose assessment, one week after exposure via Thermoluminescent dosimeters (TLDs) and DC, yielded a physical dose of 438.8 mGy and a biological dose of 398 mGy respectively.
View Article and Find Full Text PDFInt J Radiat Biol
August 2025
Authority for Nuclear Safety and Radiation Protection (ASNR), PSE-SANTE/SERAMED, Fontenay-aux-Roses, France.
Purpose: In case of an accidental or malevolent radiological event involving a large number of potential victims, fast and correct classification in terms of level of exposure is of utmost importance, not only for those that require specific medical treatment, but also for those that were not exposed. Our goal was to develop a system allowing to classify as many potential victims as possible in our laboratory by using the reference cytogenetic biodosimetry assay.
Materials And Methods: A system was created with a theoretical classification of 320 individuals 13 days after sample reception by using a triage-mode dicentric chromosome assay (DCA).