ReviewProgress in molecular and subcellular biology2026
DNA Damage and Skin Injuries Caused by Ionizing Radiation and Strategies for Wound Healing.
Review in Progress in molecular and subcellular biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Exposure to ionizing radiation can cause severe skin damage, leading to the development of cutaneous radiation syndrome. Wound healing of radiation-induced skin injuries proceeds in defined phases that depend on the intensity and type of radiation exposure. Skin damage caused by ionizing radiation can occur not only through accidental exposure, as in the case of the Chernobyl disaster, but also during radiotherapy of tumor patients. The extent of cell damage by ionizing radiation is greater in the presence of oxygen ("oxygen-effect"), most likely by the generation of reactive oxygen species (ROS), which cause damage to macromolecules (nucleic acids, proteins, lipoproteins, and polymeric carbohydrate compounds). If DNA lesions are not repaired, cells can die by apoptosis. This chapter describes the application of sensitive high-throughput microplate assays to determine the frequency of single- and double-strand DNA breaks in individuals exposed during cleanup work at the Chernobyl reactor ("liquidators"), in personnel who had worked in the destroyed Unit IV of the reactor, and in radiotherapy patients. In addition, new materials based on chitin-glucan-melanin complexes (ChGMC) and melanin-glucan complexes (MGC) or on the regeneratively active polymer inorganic polyphosphate (polyP) are presented to prevent the induction and accelerate the healing of radiation-induced skin damage.
Indexed as
Identifiers
41733680What Socratic holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.