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Status: Bibliographieeintrag

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Verfasst von:Beckermann, Benjamin Michael [VerfasserIn]   i
 Kallifatidis, Georgios [VerfasserIn]   i
 Groth, Ariane [VerfasserIn]   i
 Frommhold, David [VerfasserIn]   i
 Apel, Anja [VerfasserIn]   i
 Mattern, Jürgen [VerfasserIn]   i
 Salnikov, Alexey V. [VerfasserIn]   i
 Moldenhauer, Gerhard [VerfasserIn]   i
 Wagner, Wolfgang [VerfasserIn]   i
 Diehlmann, Anke [VerfasserIn]   i
 Saffrich, Rainer [VerfasserIn]   i
 Schubert, Mario [VerfasserIn]   i
 Ho, Anthony Dick [VerfasserIn]   i
 Giese, Nathalia [VerfasserIn]   i
 Büchler, Markus W. [VerfasserIn]   i
 Friess, Helmut [VerfasserIn]   i
 Büchler, Peter [VerfasserIn]   i
 Herr, Ingrid [VerfasserIn]   i
Titel:VEGF expression by mesenchymal stem cells contributes to angiogenesis in pancreatic carcinoma
Verf.angabe:B.M. Beckermann, G. Kallifatidis, A. Groth, D. Frommhold, A. Apel, J Mattern, A.V. Salnikov, G. Moldenhauer, W. Wagner, A. Diehlmann, R. Saffrich, M. Schubert, A.D. Ho, N. Giese, M.W. Büchler, H. Friess, P. Büchler and I. Herr
E-Jahr:2008
Jahr:29 July 2008
Umfang:10 S.
Illustrationen:Illustrationen
Fussnoten:Gesehen am 07.10.2021
Titel Quelle:Enthalten in: British journal of cancer
Ort Quelle:Edinburgh : Nature Publ. Group, 1999
Jahr Quelle:2008
Band/Heft Quelle:99(2008), 4, Seite 622-631
ISSN Quelle:1532-1827
Abstract:Little is known about the factors that enable the mobilisation of human mesenchymal stem cells (MSC) from the bone marrow into the blood stream and their recruitment to and retention in the tumour. We found specific migration of MSC towards growth factors present in pancreatic tumours, such as PDGF, EGF, VEGF and specific inhibitors Glivec, Erbitux and Avastin interfered with migration. Within a few hours, MSC migrated into spheroids consisting of pancreatic cancer cells, fibroblasts and endothelial cells as measured by time-lapse microscopy. Supernatant from subconfluent MSC increased sprouting of HUVEC due to VEGF production by MSC itself as demonstrated by RT-PCR and ELISA. Only few MSCs were differentiated into endothelial cells in vitro, whereas in vivo differentiation was not observed. Lentiviral GFP-marked MSCs, injected in nude mice xenografted with orthotopic pancreatic tumours, preferentially migrated into the tumours as observed by FACS analysis of green fluorescent cells. By immunofluorescence and intravital microscopic studies, we found the interaction of MSC with the endothelium of blood vessels. Mesenchymal stem cells supported tumour angiogenesis in vivo, that is CD31+ vessel density was increased after the transfer of MSC compared with siVEGF-MSC. Our data demonstrate the migration of MSC toward tumour vessels and suggest a supportive role in angiogenesis.
DOI:doi:10.1038/sj.bjc.6604508
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.1038/sj.bjc.6604508
 Volltext: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2527820/
 DOI: https://doi.org/10.1038/sj.bjc.6604508
Datenträger:Online-Ressource
Sprache:eng
K10plus-PPN:1772776017
Verknüpfungen:→ Zeitschrift

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