<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(22)</volume><submitter>Xiao Y</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Disruption of the DNA damage repair (DDR) gene is related to cancer progression, treatment selection, and is subjected to radiation and targeted therapies with limited success. This paper conducted a comprehensive analysis to explore the distribution of DDR mutations in Chinese pan-cancer patients.&lt;h4>Methods&lt;/h4>A total of 10,284 consecutive cases were analyzed in 24 cancer types [non-small cell lung cancer (NSCLC) 29.0%, liver 12.0%, colorectum 10.7%, etc.]. Tumor tissue samples were subjected to next generation sequencing (NGS) using a 381 gene panel incorporating 100 microsatellite loci. The association of deleterious somatic DDR mutation (del-sDDR&lt;sup>mut&lt;/sup>) with tumor mutational burden (TMB), microsatellite instability (MSI), programmed cell death-ligand 1 (PD-</pubmed_abstract><journal>Annals of translational medicine</journal><pagination>1661</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8667116</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Comprehensive analysis of DNA damage repair deficiency in 10,284 pan-cancer study.</pubmed_title><pmcid>PMC8667116</pmcid><pubmed_authors>Xie W</pubmed_authors><pubmed_authors>Zheng Y</pubmed_authors><pubmed_authors>Lei M</pubmed_authors><pubmed_authors>Zhu Z</pubmed_authors><pubmed_authors>Yang L</pubmed_authors><pubmed_authors>Wang C</pubmed_authors><pubmed_authors>Xiao Y</pubmed_authors><pubmed_authors>Huang M</pubmed_authors><pubmed_authors>Lu D</pubmed_authors><pubmed_authors>Lin Y</pubmed_authors><pubmed_authors>Zhao X</pubmed_authors><pubmed_authors>Li Z</pubmed_authors><pubmed_authors>Chen Y</pubmed_authors><pubmed_authors>Zhao J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Comprehensive analysis of DNA damage repair deficiency in 10,284 pan-cancer study.</name><description>&lt;h4>Background&lt;/h4>Disruption of the DNA damage repair (DDR) gene is related to cancer progression, treatment selection, and is subjected to radiation and targeted therapies with limited success. This paper conducted a comprehensive analysis to explore the distribution of DDR mutations in Chinese pan-cancer patients.&lt;h4>Methods&lt;/h4>A total of 10,284 consecutive cases were analyzed in 24 cancer types [non-small cell lung cancer (NSCLC) 29.0%, liver 12.0%, colorectum 10.7%, etc.]. Tumor tissue samples were subjected to next generation sequencing (NGS) using a 381 gene panel incorporating 100 microsatellite loci. The association of deleterious somatic DDR mutation (del-sDDR&lt;sup>mut&lt;/sup>) with tumor mutational burden (TMB), microsatellite instability (MSI), programmed cell death-ligand 1 (PD-</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Nov</publication><modification>2025-06-01T03:23:16.303Z</modification><creation>2025-06-01T03:23:16.303Z</creation></dates><accession>S-EPMC8667116</accession><cross_references><pubmed>34988170</pubmed><doi>10.21037/atm-21-5449</doi></cross_references></HashMap>