Publications by authors named "S Hornhardt"

Background: Sensitivity to ionizing radiation differs between individuals, but there is a limited understanding of the biological mechanisms that account for these variations. One example of such mechanisms are the mutations in the ATM (mutated ataxia telangiectasia) gene, that cause the rare recessively inherited disease Ataxia telangiectasia (AT). Hallmark features include chromosomal instability and increased sensitivity to ionizing radiation (IR).

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Objective: Head and neck cancer (HNC) accounts for almost 890,000 new cases per year. Radiotherapy (RT) is used to treat the majority of these patients. A common side-effect of RT is the onset of oral mucositis, which decreases the quality of life and represents the major dose-limiting factor in RT.

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Purpose: To establish stable growth of keratinocytes from very small biopsy specimens and successfully apply new test systems to determine their radiosensitivity.

Materials And Methods: Oral mucosa biopsies (diameter: 1.7 mm) from 15 subjects were immobilized with custom-made cups onto culture plates.

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Childhood leukemia (CL) is undoubtedly caused by a multifactorial process with genetic as well as environmental factors playing a role. But in spite of several efforts in a variety of scientific fields, the causes of the disease and the interplay of possible risk factors are still poorly understood. To push forward the research on the causes of CL, the German Federal Office for Radiation Protection has been organizing recurring international workshops since 2008 every two to three years.

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Article Synopsis
  • - Ataxia-telangiectasia (AT) is a rare genetic disorder caused by a mutation in the ATM gene, leading to issues like chromosomal instability, cancer risk, and heightened sensitivity to radiation.
  • - The study examined DNA damage and repair in lymphocytes from 8 AT patients and 10 healthy individuals after radiation exposure, finding varied responses among patients regarding γH2A.X foci and DNA repair capacity.
  • - Results indicated that while γH2A.X foci may not reliably indicate radiation sensitivity due to individual mutation differences, complex chromosomal aberrations and dicentric chromosomes could serve as effective biomarkers for assessing radiation sensitivity in AT patients.
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