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Modelling Heterogeneous Anomalous Dynamics of Radiation-Induced Double-Strand Breaks in DNA during Non-Homologous End-Joining Pathway.
Korabel, Nickolay; Warmenhoven, John W; Henthorn, Nicholas T; Ingram, Samuel; Fedotov, Sergei; Heaven, Charlotte J; Kirkby, Karen J; Taylor, Michael J; Merchant, Michael J.
Afiliação
  • Korabel N; Department of Mathematics, The University of Manchester, Manchester M13 9PL, UK.
  • Warmenhoven JW; Division of Cancer Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester M13 9PL, UK.
  • Henthorn NT; The Christie NHS Foundation Trust, Manchester M20 4BX, UK.
  • Ingram S; Division of Cancer Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester M13 9PL, UK.
  • Fedotov S; The Christie NHS Foundation Trust, Manchester M20 4BX, UK.
  • Heaven CJ; Division of Cancer Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester M13 9PL, UK.
  • Kirkby KJ; Christie Medical Physics and Engineering, The Christie NHS Foundation Trust, Manchester M20 4BX, UK.
  • Taylor MJ; Department of Mathematics, The University of Manchester, Manchester M13 9PL, UK.
  • Merchant MJ; Division of Cancer Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester M13 9PL, UK.
Entropy (Basel) ; 26(6)2024 Jun 08.
Article em En | MEDLINE | ID: mdl-38920510
ABSTRACT
The process of end-joining during nonhomologous repair of DNA double-strand breaks (DSBs) after radiation damage is considered. Experimental evidence has revealed that the dynamics of DSB ends exhibit subdiffusive motion rather than simple diffusion with rare directional movement. Traditional models often overlook the rare long-range directed motion. To address this limitation, we present a heterogeneous anomalous diffusion model consisting of subdiffusive fractional Brownian motion interchanged with short periods of long-range movement. Our model sheds light on the underlying mechanisms of heterogeneous diffusion in DSB repair and could be used to quantify the DSB dynamics on a time scale inaccessible to single particle tracking analysis. The model predicts that the long-range movement of DSB ends is responsible for the misrepair of DSBs in the form of dicentric chromosome lesions.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article