<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Liberal FDCG</submitter><funding>UK Research and Innovation</funding><pagination>7861</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10178060</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(9)</volume><pubmed_abstract>Intrinsic radiosensitivity is a major determinant of radiation response. Despite the extensive amount of radiobiological data available, variability among different studies makes it very difficult to produce high-quality radiosensitivity biomarkers or predictive models. Here, we characterize a panel of 27 human cell lines, including those derived from lung cancer, prostate cancer, and normal tissues. In addition, we used CRISPR-Cas9 to generate a panel of lines with known DNA repair defects. These cells were characterised by measuring a range of biological features, including the induction and repair of DNA double-strand breaks (DSBs), cell cycle distribution, ploidy, and clonogenic survival following X-ray irradiation. These results offer a robust dataset without inter-experimental variab</pubmed_abstract><journal>International journal of molecular sciences</journal><pubmed_title>Characterization of Intrinsic Radiation Sensitivity in a Diverse Panel of Normal, Cancerous and CRISPR-Modified Cell Lines.</pubmed_title><pmcid>PMC10178060</pmcid><funding_grant_id>MR/T021721/1</funding_grant_id><pubmed_authors>McMahon SJ</pubmed_authors><pubmed_authors>Liberal FDCG</pubmed_authors></additional><is_claimable>false</is_claimable><name>Characterization of Intrinsic Radiation Sensitivity in a Diverse Panel of Normal, Cancerous and CRISPR-Modified Cell Lines.</name><description>Intrinsic radiosensitivity is a major determinant of radiation response. Despite the extensive amount of radiobiological data available, variability among different studies makes it very difficult to produce high-quality radiosensitivity biomarkers or predictive models. Here, we characterize a panel of 27 human cell lines, including those derived from lung cancer, prostate cancer, and normal tissues. In addition, we used CRISPR-Cas9 to generate a panel of lines with known DNA repair defects. These cells were characterised by measuring a range of biological features, including the induction and repair of DNA double-strand breaks (DSBs), cell cycle distribution, ploidy, and clonogenic survival following X-ray irradiation. These results offer a robust dataset without inter-experimental variab</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Apr</publication><modification>2025-04-04T13:51:17.36Z</modification><creation>2025-04-04T13:51:17.36Z</creation></dates><accession>S-EPMC10178060</accession><cross_references><pubmed>37175568</pubmed><doi>10.3390/ijms24097861</doi></cross_references></HashMap>