Multiple myeloma: the bone marrow microenvironment and its relation to treatment

被引:36
作者
Andrews, S. W. [1 ]
Kabrah, S. [1 ]
May, J. E. [1 ]
Donaldson, C. [2 ]
Morse, H. R. [1 ]
机构
[1] Univ W England, Fac Hlth & Appl Sci, Ctr Res Biosci, Bristol BS16 1QY, Avon, England
[2] Univ Plymouth, Sch Biomed & Healthcare Sci, Ctr Res Translat Biomed, Plymouth PL4 8AA, Devon, England
关键词
Antineoplastic agents; Cellular microenvironment; Molecular targeted therapy; Multiple myeloma; MESENCHYMAL STEM-CELLS; NF-KAPPA-B; MACROPHAGE INFLAMMATORY PROTEIN-1-ALPHA; NECROSIS-FACTOR-ALPHA; OSTEOBLAST DIFFERENTIATION; STROMAL CELLS; RECEPTOR ACTIVATOR; PLASMA-CELLS; ADHESION MOLECULES; GROWTH;
D O I
10.1080/09674845.2013.11669945
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Multiple myeloma is the most common haematological malignancy yet currently it remains incurable. For decades the mainstay in therapy has been non-targeted approaches including genotoxic agents and immunosuppressants. With myeloma predominantly affecting an elderly population, who are vulnerable to aggressive therapy, these non-specific approaches have resulted in poor survival. However, in recent years an explosion of collaborative research into myeloma has identified molecular interactions between myeloma cells and the bone marrow microenvironment as promoting myeloma development and associated complications such as bone lesions due to osteolysis. At the same time, a better understanding of the adhesion molecules, cytokines and signalling pathways involved in myeloma has led to the development of new targeted therapies, which are improving the quality of life for patients and significantly extending median patient survival.
引用
收藏
页码:110 / 120
页数:11
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