Publikation: Angiogenesis and lymphangiogenesis are downregulated in primary breast cancer
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
Core Facility der Universität Konstanz
Titel in einer weiteren Sprache
Publikationstyp
Publikationsstatus
Erschienen in
Zusammenfassung
Background: Angiogenesis and lymphangiogenesis are considered to play key roles in tumour growth, progression and metastasis. However, targeting tumour angiogenesis in clinical trials showed only modest efficacy. We therefore scrutinised the concept of tumour angiogenesis and lymphangiogenesis by analysing the expression of crucial markers involved in these processes in primary breast cancer.
Methods: We analysed the expression of angiogenic, lymphangiogenic or antiangiogenic factors, their respective receptors and specific markers for endothelial and lymphendothelial cells by quantitative real-time RT-PCR in primary breast cancer and compared the expression profiles to non-cancerous, tumour-adjacent tissues and breast tissues from healthy women.
Results: We found decreased mRNA amounts of major angiogenic and lymphangiogenic factors in tumour compared to healthy tissues, whereas antiangiogenic factors were upregulated. Concomitantly, angiogenic and lymphangiogenic receptors were downregulated in breast tumours. This antiangiogenic, antilymphangiogenic microenvironment was even more pronounced in aggressive tumours and accompanied by reduced amounts of endothelial and lymphatic endothelial cell markers.
Conclusion: Primary breast tumours are not a site of highly active angiogenesis and lymphangiogenesis. Selection for tumour cells that survive with minimal vascular supply may account for this observation in clinical apparent tumours.
Zusammenfassung in einer weiteren Sprache
Fachgebiet (DDC)
Schlagwörter
Konferenz
Rezension
Zitieren
ISO 690
BONEBERG, Eva-Maria, Daniel F. LEGLER, Melanie M. HOEFER, Christian ÖHLSCHLEGEL, Helmuth STEININGER, Laszlo FÜZESI, Gertrude M. BEER, Véronique DUPONT-LAMPERT, Florian OTTO, Gregor FÜRSTENBERGER, 2009. Angiogenesis and lymphangiogenesis are downregulated in primary breast cancer. In: British Journal of Cancer. 2009, 101(4), pp. 605-614. ISSN 0007-0920. eISSN 1532-1827. Available under: doi: 10.1038/sj.bjc.6605219BibTex
@article{Boneberg2009Angio-36608, year={2009}, doi={10.1038/sj.bjc.6605219}, title={Angiogenesis and lymphangiogenesis are downregulated in primary breast cancer}, number={4}, volume={101}, issn={0007-0920}, journal={British Journal of Cancer}, pages={605--614}, author={Boneberg, Eva-Maria and Legler, Daniel F. and Hoefer, Melanie M. and Öhlschlegel, Christian and Steininger, Helmuth and Füzesi, Laszlo and Beer, Gertrude M. and Dupont-Lampert, Véronique and Otto, Florian and Fürstenberger, Gregor} }
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/123456789/36608"> <dc:creator>Legler, Daniel F.</dc:creator> <dc:creator>Dupont-Lampert, Véronique</dc:creator> <dcterms:hasPart rdf:resource="https://kops.uni-konstanz.de/bitstream/123456789/36608/3/Boneberg_0-366112.pdf"/> <void:sparqlEndpoint rdf:resource="http://localhost/fuseki/dspace/sparql"/> <dcterms:isPartOf rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/52"/> <dspace:hasBitstream rdf:resource="https://kops.uni-konstanz.de/bitstream/123456789/36608/3/Boneberg_0-366112.pdf"/> <dcterms:isPartOf rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/28"/> <dc:contributor>Hoefer, Melanie M.</dc:contributor> <dc:creator>Boneberg, Eva-Maria</dc:creator> <dc:contributor>Öhlschlegel, Christian</dc:contributor> <dc:rights>Attribution-NonCommercial-NoDerivs 3.0 Unported</dc:rights> <dc:creator>Steininger, Helmuth</dc:creator> <dspace:isPartOfCollection rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/28"/> <dc:contributor>Legler, Daniel F.</dc:contributor> <foaf:homepage rdf:resource="http://localhost:8080/"/> <dc:creator>Otto, Florian</dc:creator> <dc:contributor>Fürstenberger, Gregor</dc:contributor> <dcterms:issued>2009</dcterms:issued> <dcterms:abstract xml:lang="eng">Background: Angiogenesis and lymphangiogenesis are considered to play key roles in tumour growth, progression and metastasis. However, targeting tumour angiogenesis in clinical trials showed only modest efficacy. We therefore scrutinised the concept of tumour angiogenesis and lymphangiogenesis by analysing the expression of crucial markers involved in these processes in primary breast cancer.<br /><br />Methods: We analysed the expression of angiogenic, lymphangiogenic or antiangiogenic factors, their respective receptors and specific markers for endothelial and lymphendothelial cells by quantitative real-time RT-PCR in primary breast cancer and compared the expression profiles to non-cancerous, tumour-adjacent tissues and breast tissues from healthy women.<br /><br />Results: We found decreased mRNA amounts of major angiogenic and lymphangiogenic factors in tumour compared to healthy tissues, whereas antiangiogenic factors were upregulated. Concomitantly, angiogenic and lymphangiogenic receptors were downregulated in breast tumours. This antiangiogenic, antilymphangiogenic microenvironment was even more pronounced in aggressive tumours and accompanied by reduced amounts of endothelial and lymphatic endothelial cell markers.<br /><br />Conclusion: Primary breast tumours are not a site of highly active angiogenesis and lymphangiogenesis. Selection for tumour cells that survive with minimal vascular supply may account for this observation in clinical apparent tumours.</dcterms:abstract> <dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2017-01-12T08:30:25Z</dc:date> <dc:creator>Beer, Gertrude M.</dc:creator> <dc:contributor>Füzesi, Laszlo</dc:contributor> <dcterms:title>Angiogenesis and lymphangiogenesis are downregulated in primary breast cancer</dcterms:title> <bibo:uri rdf:resource="https://kops.uni-konstanz.de/handle/123456789/36608"/> <dc:contributor>Steininger, Helmuth</dc:contributor> <dc:creator>Hoefer, Melanie M.</dc:creator> <dcterms:available rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2017-01-12T08:30:25Z</dcterms:available> <dc:language>eng</dc:language> <dc:creator>Fürstenberger, Gregor</dc:creator> <dcterms:rights rdf:resource="http://creativecommons.org/licenses/by-nc-nd/3.0/"/> <dc:creator>Füzesi, Laszlo</dc:creator> <dspace:isPartOfCollection rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/52"/> <dc:creator>Öhlschlegel, Christian</dc:creator> <dc:contributor>Boneberg, Eva-Maria</dc:contributor> <dc:contributor>Dupont-Lampert, Véronique</dc:contributor> <dc:contributor>Beer, Gertrude M.</dc:contributor> <dc:contributor>Otto, Florian</dc:contributor> </rdf:Description> </rdf:RDF>