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Barnard, S.G.R.* ; McCarron, R.* ; Mancuso, M.* ; De Stefano, I.* ; Pazzaglia, S.* ; Pawliczek, D. ; Dalke, C. ; Ainsbury, E.A.*

Radiation-induced DNA damage and repair in lens epithelial cells of both Ptch1(+/-) and Ercc2(+/-) mutated mice.

Radiat. Res. 197, 36-42 (2021)
Postprint DOI PMC
Open Access Green
Epidemiological studies suggest an increased incidence and risk of cataract after low-dose (<2 Gy) ionizing radiation exposures. However, the biological mechanism(s) of this process are not fully understood. DNA damage and repair are thought to have a contributing role in radiation-induced cataractogenesis. Recently we have reported an inverse dose-rate effect, as well as the low-dose response, of DNA damage and repair in lens epithelial cells (LECs). Here, we present further initial findings from two mutated strains (Ercc2+/- and Ptch1+/-) of mice, both reportedly susceptible to radiation-induced cataract, and their DNA damage and repair response to low-dose and low-dose-rate gamma rays. Our results support the hypothesis that the lens epithelium responds differently to radiation than other tissues, with reported radiation susceptibility to DNA damage not necessarily translating to the LECs. Genetic predisposition and strain(s) of mice have a significant role in radiation-induced cataract susceptibility.
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Publication type Article: Journal article
Document type Scientific Article
Keywords Hedgehog Signaling Pathway; Ionizing-radiation; Mouse Lens; X-ray; Induced Cataracts; Cataractogenesis; Mechanisms; Cancer; Irradiation; Deficiency
Language english
Publication Year 2021
HGF-reported in Year 2021
ISSN (print) / ISBN 0033-7587
e-ISSN 1938-5404
Quellenangaben Volume: 197, Issue: 1, Pages: 36-42 Article Number: , Supplement: ,
Publisher Radiation Research Society
Publishing Place 810 E Tenth Street, Lawrence, Ks 66044 Usa
Reviewing status Peer reviewed
POF-Topic(s) 30203 - Molecular Targets and Therapies
Research field(s) Genetics and Epidemiology
PSP Element(s) G-506900-001
Grants Euratom Research and Training Programme 2014-2018
Scopus ID 85123324364
PubMed ID 33652474
Erfassungsdatum 2021-04-28