<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>96(14)</volume><submitter>Roperch JP</submitter><pubmed_abstract>We have previously described biological model systems for studying tumor suppression in which, by using H-1 parvovirus as a selective agent, cells with a strongly suppressed malignant phenotype (KS or US) were derived from malignant cell lines (K562 or U937). By using cDNA display on the K562/KS cells, 15 cDNAs were now isolated, corresponding to genes differentially regulated in tumor suppression. Of these, TSAP9 corresponds to a TCP-1 chaperonin, TSAP13 to a regulatory proteasome subunit, and TSAP21 to syntaxin 11, a vesicular trafficking molecule. The 15 cDNAs were used as a molecular fingerprint in different tumor-suppression models. We found that a similar pattern of differential regulation is shared by activation of p53, p21(Waf1), and the human homologue of Drosophila seven in absen</pubmed_abstract><journal>Proceedings of the National Academy of Sciences of the United States of America</journal><pagination>8070-3</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC22189</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>SIAH-1 promotes apoptosis and tumor suppression through a network involving the regulation of protein folding, unfolding, and trafficking: identification of common effectors with p53 and p21(Waf1).</pubmed_title><pmcid>PMC22189</pmcid><pubmed_authors>Nemani M</pubmed_authors><pubmed_authors>Dausset J</pubmed_authors><pubmed_authors>Pasturaud P</pubmed_authors><pubmed_authors>Telerman A</pubmed_authors><pubmed_authors>Lethrone F</pubmed_authors><pubmed_authors>Israeli D</pubmed_authors><pubmed_authors>Amson RB</pubmed_authors><pubmed_authors>Roperch JP</pubmed_authors><pubmed_authors>Prieur S</pubmed_authors><pubmed_authors>Gendron MC</pubmed_authors><pubmed_authors>Tuynder M</pubmed_authors><pubmed_authors>Oren M</pubmed_authors><pubmed_authors>Piouffre L</pubmed_authors></additional><is_claimable>false</is_claimable><name>SIAH-1 promotes apoptosis and tumor suppression through a network involving the regulation of protein folding, unfolding, and trafficking: identification of common effectors with p53 and p21(Waf1).</name><description>We have previously described biological model systems for studying tumor suppression in which, by using H-1 parvovirus as a selective agent, cells with a strongly suppressed malignant phenotype (KS or US) were derived from malignant cell lines (K562 or U937). By using cDNA display on the K562/KS cells, 15 cDNAs were now isolated, corresponding to genes differentially regulated in tumor suppression. Of these, TSAP9 corresponds to a TCP-1 chaperonin, TSAP13 to a regulatory proteasome subunit, and TSAP21 to syntaxin 11, a vesicular trafficking molecule. The 15 cDNAs were used as a molecular fingerprint in different tumor-suppression models. We found that a similar pattern of differential regulation is shared by activation of p53, p21(Waf1), and the human homologue of Drosophila seven in absen</description><dates><release>1999-01-01T00:00:00Z</release><publication>1999 Jul</publication><modification>2025-05-29T19:44:30.789Z</modification><creation>2019-03-27T00:17:49Z</creation></dates><accession>S-EPMC22189</accession><cross_references><pubmed>10393949</pubmed><doi>10.1073/pnas.96.14.8070</doi></cross_references></HashMap>