<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Winkler C</submitter><funding>Cancer Research UK</funding><funding>EC | European Regional Development Fund</funding><funding>Claudia Winkler is supported by an AstraZeneca PostDoc Fellowship funding.</funding><funding>Wellcome Trust</funding><pagination>951-962</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7921667</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>124(5)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Schlafen 11 (SLFN11) has been linked with response to DNA-damaging agents (DDA) and PARP inhibitors. An in-depth understanding of several aspects of its role as a biomarker in cancer is missing, as is a comprehensive analysis of the clinical significance of SLFN11 as a predictive biomarker to DDA and/or DNA damage-response inhibitor (DDRi) therapies.&lt;h4>Methods&lt;/h4>We used a multidisciplinary effort combining specific immunohistochemistry, pharmacology tests, anticancer combination therapies and mechanistic studies to assess SLFN11 as a potential biomarker for stratification of patients treated with several DDA and/or DDRi in the preclinical and clinical setting.&lt;h4>Results&lt;/h4>SLFN11 protein associated with both preclinical and patient treatment response to DDA, but not</pubmed_abstract><journal>British journal of cancer</journal><pubmed_title>SLFN11 informs on standard of care and novel treatments in a wide range of cancer models.</pubmed_title><pmcid>PMC7921667</pmcid><funding_grant_id>206194</funding_grant_id><funding_grant_id>FIS [PI17/01080]</funding_grant_id><funding_grant_id>Miguel Servet [CP14/00228]</funding_grant_id><funding_grant_id>Transcan-2 TH4RESPONS (AC15/00063)</funding_grant_id><funding_grant_id>22897</funding_grant_id><pubmed_authors>Armenia J</pubmed_authors><pubmed_authors>Leo E</pubmed_authors><pubmed_authors>Coker EA</pubmed_authors><pubmed_authors>Tobalina L</pubmed_authors><pubmed_authors>Baird T</pubmed_authors><pubmed_authors>Winkler C</pubmed_authors><pubmed_authors>Wang AT</pubmed_authors><pubmed_authors>Jones GN</pubmed_authors><pubmed_authors>O'Connor MJ</pubmed_authors><pubmed_authors>Pierce AJ</pubmed_authors><pubmed_authors>Sale MJ</pubmed_authors><pubmed_authors>Lau A</pubmed_authors><pubmed_authors>Petreus T</pubmed_authors><pubmed_authors>Jaaks P</pubmed_authors><pubmed_authors>Serra V</pubmed_authors><pubmed_authors>Garnett MJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>SLFN11 informs on standard of care and novel treatments in a wide range of cancer models.</name><description>&lt;h4>Background&lt;/h4>Schlafen 11 (SLFN11) has been linked with response to DNA-damaging agents (DDA) and PARP inhibitors. An in-depth understanding of several aspects of its role as a biomarker in cancer is missing, as is a comprehensive analysis of the clinical significance of SLFN11 as a predictive biomarker to DDA and/or DNA damage-response inhibitor (DDRi) therapies.&lt;h4>Methods&lt;/h4>We used a multidisciplinary effort combining specific immunohistochemistry, pharmacology tests, anticancer combination therapies and mechanistic studies to assess SLFN11 as a potential biomarker for stratification of patients treated with several DDA and/or DDRi in the preclinical and clinical setting.&lt;h4>Results&lt;/h4>SLFN11 protein associated with both preclinical and patient treatment response to DDA, but not</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Mar</publication><modification>2026-07-16T01:56:45.094Z</modification><creation>2026-07-09T10:36:42.501Z</creation></dates><accession>S-EPMC7921667</accession><cross_references><pubmed>33339894</pubmed><doi>10.1038/s41416-020-01199-4</doi></cross_references></HashMap>