The pathogenesis of the bone disease of multiple myeloma

被引:163
作者
Edwards, Claire M. [1 ]
Zhuang, Junling [1 ]
Mundy, Gregory R. [2 ]
机构
[1] Vanderbilt Univ, Dept Canc Biol, Vanderbilt Ctr Bone Biol, Nashville, TN 37203 USA
[2] Vanderbilt Univ, Dept Med Clin Pharmacol, Vanderbilt Ctr Bone Biol, Nashville, TN USA
关键词
multiple myeloma; osteoclast; osteoblast; RANKL; Dkk1;
D O I
10.1016/j.bone.2008.01.027
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Multiple myeloma is a fatal hematologic malignancy associated with clonal expansion of malignant plasma cells within the bone marrow and the development of a destructive osteolytic bone disease. The principal cellular mechanisms involved in the development of myeloma bone disease are an increase in osteoclastic bone resorption, and a reduction in bone formation. Myeloma cells are found in close association with sites of active bone resorption, and the interactions between myeloma cells and other cells within the specialized bone marrow microenvironment are essential, both for tumor growth and the development of myeloma bone disease. This review discusses the many different factors which have been implicated in myeloma bone disease, including the evidence for their role in myeloma and subsequent therapeutic implications. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:1007 / 1013
页数:7
相关论文
共 84 条
[1]
Osteoclasts enhance myeloma cell growth and survival via cell-cell contact: a vicious cycle between bone destruction and myeloma expansion [J].
Abe, M ;
Hiura, K ;
Wilde, J ;
Shioyasono, A ;
Moriyama, K ;
Hashimoto, T ;
Kido, S ;
Oshima, T ;
Shibata, H ;
Ozaki, S ;
Inoue, D ;
Matsumoto, T .
BLOOD, 2004, 104 (08) :2484-2491
[2]
Abildgaard N, 1998, EUR J HAEMATOL, V61, P128
[3]
Mechanisms of regulation of CXCR4/SDF-1 (CXCL12)-dependent migration and homing in multiple myeloma [J].
Alsayed, Yazan ;
Ngo, Hai ;
Runnels, Judith ;
Leleu, Xavier ;
Singha, Ujjal K. ;
Pitsillides, Costas M. ;
Spencer, Joel A. ;
Kimlinger, Teresa ;
Ghobrial, Joanna M. ;
Jia, Xiaoying ;
Lu, Ganwei ;
Timm, Michael ;
Kumar, Ashok ;
Cote, Daniel ;
Veilleux, Israel ;
Hedin, Karen E. ;
Roodman, G. David ;
WitZig, Thomas E. ;
Kung, Andrew L. ;
Hideshima, Teru ;
Anderson, Kenneth C. ;
Lin, Charles P. ;
Ghobrial, Irene M. .
BLOOD, 2007, 109 (07) :2708-2717
[4]
Syndecan-1 and angiogenic cytokines in multiple myeloma: correlation with bone marrow angiogenesis and survival [J].
Andersen, NF ;
Standal, T ;
Nielsen, JL ;
Heickendorff, L ;
Borset, M ;
Sorensen, FB ;
Abildgaard, N .
BRITISH JOURNAL OF HAEMATOLOGY, 2005, 128 (02) :210-217
[5]
A homologue of the TNF receptor and its ligand enhance T-cell growth and dendritic-cell function [J].
Anderson, DM ;
Maraskovsky, E ;
Billingsley, WL ;
Dougall, WC ;
Tometsko, ME ;
Roux, ER ;
Teepe, MC ;
DuBose, RF ;
Cosman, D ;
Galibert, L .
NATURE, 1997, 390 (6656) :175-179
[6]
RECRUITMENT OF NEW OSTEOBLASTS AND OSTEOCLASTS IS THE EARLIEST CRITICAL EVENT IN THE PATHOGENESIS OF HUMAN MULTIPLE-MYELOMA [J].
BATAILLE, R ;
CHAPPARD, D ;
MARCELLI, C ;
DESSAUW, P ;
BALDET, P ;
SANY, J ;
ALEXANDRE, C .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 88 (01) :62-66
[7]
BATAILLE R, 1990, CANCER-AM CANCER SOC, V66, P167, DOI 10.1002/1097-0142(19900701)66:1<167::AID-CNCR2820660130>3.0.CO
[8]
2-9
[9]
A study of the biological receptor activator of nuclear factor-κB ligand inhibitor, denosumab, in patients with multiple myeloma or bone metastases from breast cancer [J].
Body, JJ ;
Facon, T ;
Coleman, RE ;
Lipton, A ;
Geurs, F ;
Fan, M ;
Holloway, D ;
Peterson, MC ;
Bekker, P .
CLINICAL CANCER RESEARCH, 2006, 12 (04) :1221-1228
[10]
A phase I study of AMGN-0007, a recombinant osteoprotegerin construct, in patients with multiple myeloma or breast carcinoma related bone metastases [J].
Body, JJ ;
Greipp, P ;
Coleman, RE ;
Facon, T ;
Geurs, F ;
Fermand, JP ;
Harousseau, JL ;
Lipton, A ;
Mariette, X ;
Williams, CD ;
Nakanishi, A ;
Holloway, D ;
Martin, SW ;
Dunstan, CR ;
Bekker, PJ .
CANCER, 2003, 97 (03) :887-892