Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.14279/1824
Title: P-selectin Glycoprotein Ligand Regulates the Interaction of Multiple Myeloma Cells with the Bone Marrow Microenvironment
Authors: Azab, Abdel Kareem 
Quang, Phong 
Pitsillides, Costas 
Azab, Feda 
Thompson, Brian 
Chonghaile, Triona 
Patton, John T. 
Maiso, Patricia 
Monrose, Val 
Sacco, Antonio 
Ngo, Hai T. 
Flores, Ludmila M. 
Lin, Charles P. 
Magnani, John L. 
Kung, Andrew L. 
Letai, Anthony 
Carrasco, Ruben 
Roccaro, Aldo M. 
Ghobrial, Irene M. 
Major Field of Science: Natural Sciences
Keywords: Blood;Hematology;Multiple myeloma;Bone marrow;Glycoproteins;Animal experimentation;Mice
Issue Date: 9-Feb-2012
Source: Blood, 2012, vol. 119, no. 6, pp. 1468-1478
Volume: 119
Issue: 6
Start page: 1468
End page: 1478
Journal: Blood 
Abstract: Interactions between multiple myeloma (MM) cells and the BM microenvironment play a critical role in the pathogenesis of MM and in the development of drug resistance by MM cells. Selectins are involved in extravasation and homing of leukocytes to target organs. In the present study, we focused on adhesion dynamics that involve P-selectin glycoprotein ligand-1 (PSGL-1) on MM cells and its interaction with selectins in the BM microenvironment. We show that PSGL-1 is highly expressed on MM cells and regulates the adhesion and homing of MM cells to cells in the BM microenvironment in vitro and in vivo. This interaction involves both endothelial cells and BM stromal cells. Using loss-of-function studies and the small-molecule pan-selectin inhibitor GMI-1070, we show that PSGL-1 regulates the activation of integrins and downstream signaling. We also document that this interaction regulates MM-cell proliferation in coculture with BM microenvironmental cells and the development of drug resistance. Furthermore, inhibiting this interaction with GMI-1070 enhances the sensitization of MM cells to bortezomib in vitro and in vivo. These data highlight the critical contribution of PSGL-1 to the regulation of growth, dissemination, and drug resistance in MM in the context of the BM microenvironment
URI: https://hdl.handle.net/20.500.14279/1824
ISSN: 15280020
DOI: 10.1182/blood-2011-07-368050
Rights: © 2012 by The American Society of Hematology
Type: Article
Affiliation: Massachusetts General Hospital 
Affiliation : Dana-Farber Cancer Institute 
Massachusetts General Hospital 
Harvard University 
GlycoMimetics 
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