Lenalidomide inhibits osteoclastogenesis, survival factors and bone-remodeling markers in multiple myeloma
暂无分享,去创建一个
K. Anderson | N. Munshi | P. Richardson | C. Mitsiades | D. Chauhan | N. Raje | T. Hideshima | M. Raab | Y. Okawa | S. Vallet | I. Breitkreutz | K. Anderson
[1] F. Zhan,et al. Atacicept (TACI-Ig) inhibits growth of TACIhigh primary myeloma cells in SCID-hu mice and in coculture with osteoclasts , 2008, Leukemia.
[2] Michael Wang,et al. Lenalidomide plus dexamethasone for relapsed multiple myeloma in North America. , 2007, The New England journal of medicine.
[3] Alessandro Corso,et al. Lenalidomide plus dexamethasone for relapsed or refractory multiple myeloma. , 2007, The New England journal of medicine.
[4] O. Sezer,et al. Bortezomib inhibits human osteoclastogenesis , 2007, Leukemia.
[5] M. Dimopoulos,et al. Bortezomib reduces serum dickkopf‐1 and receptor activator of nuclear factor‐κB ligand concentrations and normalises indices of bone remodelling in patients with relapsed multiple myeloma , 2006, British journal of haematology.
[6] Diane Warren,et al. A randomized phase 2 study of lenalidomide therapy for patients with relapsed or relapsed and refractory multiple myeloma. , 2006, Blood.
[7] N. Munshi,et al. Role of B-cell-activating factor in adhesion and growth of human multiple myeloma cells in the bone marrow microenvironment. , 2006, Cancer research.
[8] M. Abe,et al. BAFF and APRIL as osteoclast-derived survival factors for myeloma cells: a rationale for TACI-Fc treatment in patients with multiple myeloma , 2006, Leukemia.
[9] A. Donnenberg,et al. Thalidomide derivative CC-4047 inhibits osteoclast formation by down-regulation of PU.1. , 2005, Blood.
[10] M. Dimopoulos,et al. The combination of intermediate doses of thalidomide with dexamethasone is an effective treatment for patients with refractory/relapsed multiple myeloma and normalizes abnormal bone remodeling, through the reduction of sRANKL/osteoprotegerin ratio , 2005, Leukemia.
[11] D. Esseltine,et al. Response to bortezomib is associated to osteoblastic activation in patients with multiple myeloma , 2005, British journal of haematology.
[12] V. Pantesco,et al. The level of TACI gene expression in myeloma cells is associated with a signature of microenvironment dependence versus a plasmablastic signature. , 2005, Blood.
[13] Hartmut Goldschmidt,et al. Bortezomib or high-dose dexamethasone for relapsed multiple myeloma. , 2005, The New England journal of medicine.
[14] D. Esseltine,et al. A phase 2 study of two doses of bortezomib in relapsed or refractory myeloma , 2004, British journal of haematology.
[15] K. Tarte,et al. BAFF and APRIL protect myeloma cells from apoptosis induced by IL-6 deprivation and dexamethasone , 2003 .
[16] N. Callander,et al. And Growth of Myeloma Cells Il-3 Expression by Myeloma Cells Increases Both Osteoclast Formation , 2022 .
[17] F. Zhan,et al. The role of the Wnt-signaling antagonist DKK1 in the development of osteolytic lesions in multiple myeloma. , 2003, The New England journal of medicine.
[18] L. To,et al. Receptor activator of nuclear factor-kappaB ligand expression by human myeloma cells mediates osteoclast formation in vitro and correlates with bone destruction in vivo. , 2003, Cancer research.
[19] J. Goldman,et al. Soluble receptor activator of nuclear factor kappaB ligand-osteoprotegerin ratio predicts survival in multiple myeloma: proposal for a novel prognostic index. , 2003, Blood.
[20] Paul J. Williams,et al. Dual effects of macrophage inflammatory protein-1alpha on osteolysis and tumor burden in the murine 5TGM1 model of myeloma bone disease. , 2003, Blood.
[21] David L. Lacey,et al. Osteoclast differentiation and activation , 2003, Nature.
[22] B. Dörken,et al. Macrophage inflammatory protein 1-alpha (MIP-1 alpha ) triggers migration and signaling cascades mediating survival and proliferation in multiple myeloma (MM) cells. , 2003, Blood.
[23] L. Hofbauer,et al. RANK ligand and osteoprotegerin in myeloma bone disease. , 2003, Blood.
[24] P. Croucher,et al. Recombinant osteoprotegerin decreases tumor burden and increases survival in a murine model of multiple myeloma. , 2003, Cancer research.
[25] Hiroshi Takayanagi,et al. Induction and activation of the transcription factor NFATc1 (NFAT2) integrate RANKL signaling in terminal differentiation of osteoclasts. , 2002, Developmental cell.
[26] T. Hideshima,et al. Molecular mechanisms of novel therapeutic approaches for multiple myeloma , 2002, Nature Reviews Cancer.
[27] K. Moriyama,et al. Role for macrophage inflammatory protein (MIP)-1α and MIP-1β in the development of osteolytic lesions in multiple myeloma , 2002 .
[28] G. Giannelli,et al. Localization and possible role of two different alpha v beta 3 integrin conformations in resting and resorbing osteoclasts. , 2002, Journal of cell science.
[29] P. Richardson,et al. Novel therapies targeting the myeloma cell and its bone marrow microenvironment. , 2001, Seminars in oncology.
[30] N. Callander,et al. Myeloma bone disease. , 2001, Seminars in hematology.
[31] G. Roodman,et al. Macrophage inflammatory protein-1alpha is an osteoclastogenic factor in myeloma that is independent of receptor activator of nuclear factor kappaB ligand. , 2001, Blood.
[32] I. James,et al. Biosynthesis and processing of cathepsin K in cultured human osteoclasts. , 2001, Bone.
[33] Amy S Orr,et al. BLyS: member of the tumor necrosis factor family and B lymphocyte stimulator. , 1999, Science.
[34] J. Tschopp,et al. APRIL, a New Ligand of the Tumor Necrosis Factor Family, Stimulates Tumor Cell Growth , 1998, The Journal of experimental medicine.
[35] S. Mckercher,et al. Osteopetrosis in mice lacking haematopoietic transcription factor PU.1 , 1997, Nature.
[36] M. Kovacs,et al. Efficacy of pamidronate in reducing skeletal events in patients with advanced multiple myeloma. Myeloma Aredia Study Group. , 1996, The New England journal of medicine.
[37] E. Wagner,et al. c-Fos: a key regulator of osteoclast-macrophage lineage determination and bone remodeling. , 1994, Science.
[38] E. Wagner,et al. Bone and haematopoietic defects in mice lacking c-fos , 1992, Nature.
[39] K. Moriyama,et al. Role for macrophage inflammatory protein (MIP)-1alpha and MIP-1beta in the development of osteolytic lesions in multiple myeloma. , 2002, Blood.
[40] Z. Lee,et al. The phosphatidylinositol 3-kinase, p38, and extracellular signal-regulated kinase pathways are involved in osteoclast differentiation. , 2002, Bone.
[41] J. Moake,et al. Immunocytochemistry reveals RANKL expression of myeloma cells , 2002 .
[42] G. Roodman,et al. Macrophage inflammatory protein-1alpha is an osteoclastogenic factor in myeloma that is independent of receptor activator of nuclear factor kappaB ligand. , 2001, Blood.
[43] F. Craig,et al. Macrophage inflammatory protein 1-alpha is a potential osteoclast stimulatory factor in multiple myeloma. , 2000, Blood.