<HashMap><database>biostudies-other</database><scores/><additional><submitter>Chang YC</submitter><pagination>5054-5063</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-ECPF-GEOD-10856</full_dataset_link><project>EurocanPlatform</project><abstract>"Decoy receptor 3 (DcR3) is a member of the TNF receptor superfamily and is up-regulated in tumors that originate from a diversity of lineages. DcR3 is capable of promoting angiogenesis, inducing dendritic cell apoptosis, and modulating macrophage differentiation. Since tumor-associated macrophages (TAMs) are the major infiltrating leukocytes in most malignant tumors, we used microarray technology to investigate whether DcR3 contributes to the development of TAMs. Among the DcR3-modulated genes expressed by TAMs, those that encode proteins involved in MHC class II (MHC-II)-dependent antigen presentation were down-regulated substantially, together with the master regulator of MHC-II expression (the class II transactivator, CIITA). The ERK- and JNK-induced deacetylation of histones associate</abstract><repository>biostudies-other</repository><experiment_type>transcription profiling by array</experiment_type><data_source>EurocanPlatform</data_source><omics_type>Unknown</omics_type><volume>111</volume><journal>Blood</journal><species>Homo sapiens</species><pubmed_authors>Hsieh SL</pubmed_authors><pubmed_authors>Lee CT</pubmed_authors><pubmed_authors>Chen TC</pubmed_authors><pubmed_authors>Yang CY</pubmed_authors><pubmed_authors>Wang CC</pubmed_authors><pubmed_authors>Wang HW</pubmed_authors><pubmed_authors>Chang YC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Transcription profiling by array of human monocytes were cultured with DcR3 in the presence of M-CSF</name><description>"Decoy receptor 3 (DcR3) is a member of the TNF receptor superfamily and is up-regulated in tumors that originate from a diversity of lineages. DcR3 is capable of promoting angiogenesis, inducing dendritic cell apoptosis, and modulating macrophage differentiation. Since tumor-associated macrophages (TAMs) are the major infiltrating leukocytes in most malignant tumors, we used microarray technology to investigate whether DcR3 contributes to the development of TAMs. Among the DcR3-modulated genes expressed by TAMs, those that encode proteins involved in MHC class II (MHC-II)-dependent antigen presentation were down-regulated substantially, together with the master regulator of MHC-II expression (the class II transactivator, CIITA). The ERK- and JNK-induced deacetylation of histones associate</description><dates><release>2016-04-14T13:27:21Z</release><publication>2008 May</publication><modification>2016-04-14T13:27:21Z</modification><creation>2016-04-14T13:27:21Z</creation></dates><accession>S-ECPF-GEOD-10856</accession><cross_references><GEO>GSE10856</GEO><ArrayExpress>E-GEOD-10856</ArrayExpress><EFO>EFO_0000322</EFO><EFO>EFO_0000311</EFO><ArrayExpress files>E-GEOD-10856</ArrayExpress files></cross_references></HashMap>