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Neutrophil granulocyte derived MMP-9 is a VEGF independent functional component of the angiogenic switch in pancreatic ductal adenocarcinoma
Authors:Dirk Bausch  Thomas Pausch  Tobias Krauss  Ulrich Theodor Hopt  Carlos Fernandez-del-Castillo  Andrew L Warshaw  Sarah P Thayer  Tobias Keck
Institution:1.Department of General and Visceral Surgery,University of Freiburg,Freiburg,Germany;2.Klinik für Allgemein, Viszeral- und Transplantationschirurgie,Universit?t Heidelberg,Heidelberg,Germany;3.Radiologische Universit?tsklinik Freiburg i. Br.,Freiburg i. Br.,Germany;4.Department of Surgery,Massachusetts General Hospital and Harvard Medical School,Boston,USA
Abstract:

Background  

Vascular endothelial growth factor (VEGF) that is secreted by tumor cells plays a key role in angiogenesis. Matrix metalloproteinase 9 (MMP-9) is produced by inflammatory cells, such as stromal granulocytes (PMN), remodels the extracellular matrix and is known to promote angiogenesis indirectly by interacting with VEGF. The aim of this study was to determine the role of PMN-derived MMP-9, its interaction with VEGF, and the efficacy of anti-angiogenic therapy targeting MMP-9 with oral Doxycycline and VEGF with Bevacizumab in pancreatic cancer (PDAC).
Keywords:
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