<HashMap><database>biostudies-other</database><scores/><additional><submitter>Pang B</submitter><pagination>1908</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-ECPF-GEOD-33624</full_dataset_link><project>EurocanPlatform</project><abstract>One major class of anti-cancer drugs targets topoisomerase II to induce DNA double-strand breaks and cell death of fast growing cells.  Here, we compare three members of this class - the antracyclines doxorubicin and aclarubicin, and a chemically unrelated compound, etoposide. Aclarubicin does not induce DNA breaks. We define a new activity for the antracyclines: unsupported histone eviction from ´open´ or loosely packed chromosomal areas reflecting exon and promoter regions. As a result, the epigenome and the transcriptome are strongly affected. Tissue culture cells were treated with doxorubicin, aclarubicin or etoposide for 2 hours. Then drugs were removed by extensive washing. cells were further cultured for indicated days before total RNA were extracted and compared to un-treated contr</abstract><repository>biostudies-other</repository><experiment_type>transcription profiling by array</experiment_type><data_source>EurocanPlatform</data_source><omics_type>Unknown</omics_type><volume>4</volume><journal>Nature communications</journal><species>Homo sapiens</species><pubmed_authors>Pang B</pubmed_authors><pubmed_authors>van Tellingen O</pubmed_authors><pubmed_authors>Janssen J</pubmed_authors><pubmed_authors>Janssen L</pubmed_authors><pubmed_authors>Huijgens P</pubmed_authors><pubmed_authors>Kerkhoven R</pubmed_authors><pubmed_authors>Groothuis T</pubmed_authors><pubmed_authors>Rottenberg S</pubmed_authors><pubmed_authors>Zwart W</pubmed_authors><pubmed_authors>Qiao X</pubmed_authors><pubmed_authors>Neefjes J</pubmed_authors><pubmed_authors>Ovaa H</pubmed_authors><pubmed_authors>Nieuwland M</pubmed_authors><pubmed_authors>Velds A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Distinct effects of  topoisomerase II inhibitors on tumor cell lines (part 1)</name><description>One major class of anti-cancer drugs targets topoisomerase II to induce DNA double-strand breaks and cell death of fast growing cells.  Here, we compare three members of this class - the antracyclines doxorubicin and aclarubicin, and a chemically unrelated compound, etoposide. Aclarubicin does not induce DNA breaks. We define a new activity for the antracyclines: unsupported histone eviction from ´open´ or loosely packed chromosomal areas reflecting exon and promoter regions. As a result, the epigenome and the transcriptome are strongly affected. Tissue culture cells were treated with doxorubicin, aclarubicin or etoposide for 2 hours. Then drugs were removed by extensive washing. cells were further cultured for indicated days before total RNA were extracted and compared to un-treated contr</description><dates><release>2016-04-14T14:05:17Z</release><publication>2013</publication><modification>2016-04-14T14:05:17Z</modification><creation>2016-04-14T14:05:17Z</creation></dates><accession>S-ECPF-GEOD-33624</accession><cross_references><GEO>GSE33624</GEO><ArrayExpress>E-GEOD-33624</ArrayExpress><EFO>EFO_0000756</EFO><EFO>EFO_0000365</EFO><EFO>EFO_0000322</EFO><ArrayExpress files>E-GEOD-33624</ArrayExpress files></cross_references></HashMap>