Evidence for a macromolecular complex in poor prognosis CLL that contains CD38, CD49d, CD44 and MMP-9.

Andrea G S Buggins,Ana Levi,Piers E M Patten,Yolanda Calle,Deborah Yallop, J L Binet, Ariane Auquier,Guillaume Dighiero, C Chastang,H Piguet,Jeanetienne Goasguen, G Vaugier,G Potron, P Colona, F Oberling,Michael S C Thomas,Gil Tchernia,C Jacquillat, Pierre Boivin, C Lesty, M T Duault, M Monconduit,S Belabbes, F Gremy,Chris Pepper,Saman Hewamana,Satyen Gohil,Jane Moorhead,Najeemdeen Folarin,N S Thomas,Ghulam J Mufti,Chris Fegan,Stephen Devereux, Joachim Burger,Nobuhiro Tsukada, Michael Burger,Nathan J Zvaifler, M E Dellaquila,Thomas J Kipps,Federico Caligariscappio, S Burns,Adrian J Thrasher,Gareth E Jones, Mario Crespo,Francesc Bosch,Neus Villamor,Beatriz Bellosillo,Dolors Colomer,Maria Rozman,Silvia Marce,Armando Lopezguillermo,Elias Campo,Emilio Montserrat,Rajendra N Damle,Tarun Wasil,Franco Fais,Fabio Ghiotto,Angelo Valetto,Steven L Allen,Aby Buchbinder,Daniel R Budman,Kurt E J Dittmar,Jonathan E Kolitz,Stuart M Lichtman,Philip Schulman,Vincent Vinciguerra,Kanti R Rai,Manlio Ferrarini,Nicholas Chiorazzi,Silvia Deaglio,Andrea Capobianco, L Bergui,Jan Durig, Fortunato Morabito,Ulrich Duhrsen,Fabio Malavasi,Tiziana Vaisitti,Semra Aydin,Giovanni Darena,Lisa Bonello, P Omede,Maria Scatolini,Ozren Jaksic,Giovanna Chiorino,Dimitar G Efremov,Alberto L Horenstein,Luca Tamagnone, L Boumsell,Jennifer Edelmann,Ludger Kleinhitpass,Alexander Carpinteiro,Anja Fuhrer,Ludger Sellmann,Stephan Stilgenbauer,Aura S Kamiguti,Eui Seung Lee,Kathleen J Till,Robert J Harris,Mark A Glenn,Ke Lin, H J Chen,Mirko Zuzel,J C Cawley,Aneela Majid,Thet Thet Lin, G C Best,K Fishlock,Guy Pratt, S R Wagner, Barbara J Kennedy,Fiona Miall,Robert Kerrin Hills,D G Oscier, M J Dyer, J D M Richards, A Wotherspoon, J R Salisbury,T J Hamblin, B T Pittner,Tait D Shanafelt,Neil E Kay,Diane F Jelinek,Arthur Sawitsky,E P Cronkite, A D Chanana, R N Levy, B S Pasternack,Javier Redondomunoz,Estefania Ugarteberzal,Jose A Garciamarco, M H Del Cerro, P E Van Den Steen,Ghislain Opdenakker,Maria Jose Terol,Angeles Garciapardo,Susan M Geyer,Nancy D Bone,Renee C Tschumper,Thomas E Witzig,Grzegorz S Nowakowski,Clive S Zent,Timothy G Call,Betsy Laplant,Gordon W Dewald,Claudya Tenca, Adrian Merlo,Daniela Zarcone,Daniele Saverino,Silvia Bruno, A De Santanna,Dunia Ramarli,Marina Fabbi, Cecilia Calvo Pesce,Ermanno Ciccone, C E Grossi, R A Worthylake, Keith Burridge, G De Rossi,Paola Marroni,Francesca Romana Mauro, G Cerruti,Nicola Albi,Stefano Fiorucci,Andrea Velardi,Antonella Zucchetto, Daniele Benedetti,Claudio Tripodo,Riccardo Bomben,M Dal Bo, Daniele Marconi,Fleur Bossi,Debora Lorenzon,Massimo Degan,Francesca Rossi,Pietro Bulian,V Franco,G Del Poeta,Gianluca Gaidano,Francesco Tedesco,Valter Gattei

BRITISH JOURNAL OF HAEMATOLOGY(2011)

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摘要
Progressive chronic lymphocytic leukaemia is characterized by the accumulation of neoplastic B-cells in the tissues and correlates with the expression of prognostic biomarkers, such as CD38, CD49d and matrix metalloproteinase-9 (MMP9), which are involved in migration and tissue invasion. In this study we investigated the physical relationship between these molecules and demonstrated that CD38, CD49d, MMP9 and CD44 were physically associated in a supramolecular cell surface complex. Our findings provide a molecular basis for the correlation between expression of these proteins and prognosis and, as the complex is not present in normal B-cells, suggest a novel leukaemia-specific therapeutic target.
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chronic lymphocytic leukaemia,CD38,CD49d,CD44,matrix metalloproteinase-9
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