Publikation: An artificial PAP gene breaks self-tolerance and promotes tumor regression in the TRAMP model for prostate carcinoma
Dateien
Datum
Autor:innen
Herausgeber:innen
ISSN der Zeitschrift
Electronic ISSN
ISBN
Bibliografische Daten
Verlag
Schriftenreihe
Auflagebezeichnung
URI (zitierfähiger Link)
DOI (zitierfähiger Link)
Internationale Patentnummer
Link zur Lizenz
Angaben zur Forschungsförderung
Projekt
Open Access-Veröffentlichung
Sammlungen
Core Facility der Universität Konstanz
Titel in einer weiteren Sprache
Publikationstyp
Publikationsstatus
Erschienen in
Zusammenfassung
Prostate cancer (PCa) is the most commonly diagnosed type of cancer in men in western industrialized countries. As a public health burden, the need for the invention of new cost-saving PCa immunotherapies is apparent. In this study, we present a DNA vaccine encoding for the prostate-specific antigen prostatic acid phosphatase (PAP) linked to the J-domain and the SV40 enhancer sequence. The PAP DNA vaccine induced a strong PAP-specific cellular immune response after electroporation (EP)-based delivery in C57BL/6 mice. Splenocytes from mice immunized with PAP recognized the naturally processed PAP epitopes, indicating that vaccination with the PAP-J gene broke its self-tolerance against PAP. Remarkably, DNA vaccination with PAP-J inhibited tumor growth in the Transgenic Adenocarcinoma of the Mouse Prostate (TRAMP) mouse model that closely resembled human PCa. Therefore, this study highlights a novel cancer immunotherapy approach with the potential to control PCa in clinical settings.
Zusammenfassung in einer weiteren Sprache
Fachgebiet (DDC)
Schlagwörter
Konferenz
Rezension
Zitieren
ISO 690
SPIES, Elmar, Wilfried REICHARDT, Gerardo Omar ALVAREZ SALINAS, Marcus GRÖTTRUP, Peter ÖHLSCHLÄGER, 2012. An artificial PAP gene breaks self-tolerance and promotes tumor regression in the TRAMP model for prostate carcinoma. In: Molecular Therapy. 2012, 20(3), pp. 555-564. ISSN 1525-0016. eISSN 1525-0024. Available under: doi: 10.1038/mt.2011.241BibTex
@article{Spies2012-03artif-18035, year={2012}, doi={10.1038/mt.2011.241}, title={An artificial PAP gene breaks self-tolerance and promotes tumor regression in the TRAMP model for prostate carcinoma}, number={3}, volume={20}, issn={1525-0016}, journal={Molecular Therapy}, pages={555--564}, author={Spies, Elmar and Reichardt, Wilfried and Alvarez Salinas, Gerardo Omar and Gröttrup, Marcus and Öhlschläger, Peter} }
RDF
<rdf:RDF xmlns:dcterms="http://purl.org/dc/terms/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:bibo="http://purl.org/ontology/bibo/" xmlns:dspace="http://digital-repositories.org/ontologies/dspace/0.1.0#" xmlns:foaf="http://xmlns.com/foaf/0.1/" xmlns:void="http://rdfs.org/ns/void#" xmlns:xsd="http://www.w3.org/2001/XMLSchema#" > <rdf:Description rdf:about="https://kops.uni-konstanz.de/server/rdf/resource/123456789/18035"> <dc:creator>Spies, Elmar</dc:creator> <dcterms:hasPart rdf:resource="https://kops.uni-konstanz.de/bitstream/123456789/18035/2/Spies_180353.pdf"/> <dc:contributor>Öhlschläger, Peter</dc:contributor> <dcterms:available rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2012-04-04T13:38:31Z</dcterms:available> <dspace:isPartOfCollection rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/28"/> <dcterms:isPartOf rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/28"/> <dcterms:abstract xml:lang="eng">Prostate cancer (PCa) is the most commonly diagnosed type of cancer in men in western industrialized countries. As a public health burden, the need for the invention of new cost-saving PCa immunotherapies is apparent. In this study, we present a DNA vaccine encoding for the prostate-specific antigen prostatic acid phosphatase (PAP) linked to the J-domain and the SV40 enhancer sequence. The PAP DNA vaccine induced a strong PAP-specific cellular immune response after electroporation (EP)-based delivery in C57BL/6 mice. Splenocytes from mice immunized with PAP recognized the naturally processed PAP epitopes, indicating that vaccination with the PAP-J gene broke its self-tolerance against PAP. Remarkably, DNA vaccination with PAP-J inhibited tumor growth in the Transgenic Adenocarcinoma of the Mouse Prostate (TRAMP) mouse model that closely resembled human PCa. Therefore, this study highlights a novel cancer immunotherapy approach with the potential to control PCa in clinical settings.</dcterms:abstract> <dcterms:issued>2012-03</dcterms:issued> <void:sparqlEndpoint rdf:resource="http://localhost/fuseki/dspace/sparql"/> <dcterms:bibliographicCitation>Publ. in: Molecular Therapy ; 20 (2012), 3. S. 555–564</dcterms:bibliographicCitation> <dc:contributor>Spies, Elmar</dc:contributor> <bibo:uri rdf:resource="http://kops.uni-konstanz.de/handle/123456789/18035"/> <dcterms:title>An artificial PAP gene breaks self-tolerance and promotes tumor regression in the TRAMP model for prostate carcinoma</dcterms:title> <dc:creator>Alvarez Salinas, Gerardo Omar</dc:creator> <dc:creator>Reichardt, Wilfried</dc:creator> <dc:contributor>Alvarez Salinas, Gerardo Omar</dc:contributor> <dc:language>eng</dc:language> <dspace:hasBitstream rdf:resource="https://kops.uni-konstanz.de/bitstream/123456789/18035/2/Spies_180353.pdf"/> <foaf:homepage rdf:resource="http://localhost:8080/"/> <dc:contributor>Gröttrup, Marcus</dc:contributor> <dc:creator>Gröttrup, Marcus</dc:creator> <dc:creator>Öhlschläger, Peter</dc:creator> <dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2012-04-04T13:38:31Z</dc:date> <dc:rights>terms-of-use</dc:rights> <dc:contributor>Reichardt, Wilfried</dc:contributor> <dcterms:rights rdf:resource="https://rightsstatements.org/page/InC/1.0/"/> </rdf:Description> </rdf:RDF>