Macrophages in multiple myeloma: key roles and therapeutic strategies

被引:17
|
作者
Opperman, Khatora S. [1 ,2 ]
Vandyke, Kate [1 ,2 ]
Psaltis, Peter J. [3 ,4 ]
Noll, Jacqueline E. [1 ,2 ]
Zannettino, Andrew C. W. [1 ,2 ,4 ]
机构
[1] Univ Adelaide, Fac Hlth & Med Sci, Adelaide Med Sch, Myeloma Res Lab, Adelaide, SA, Australia
[2] SAHMRI, South Australian Hlth & Med Res Inst, Precis Med Theme, Canc Program, Level 5 South,POB 11060, Adelaide, SA 5001, Australia
[3] South Australian Hlth & Med Res Inst, Lifelong Hlth Theme, Vasc Res Ctr, Heart & Vasc Program, Adelaide, SA, Australia
[4] Cent Adelaide Local Hlth Network, Adelaide, SA, Australia
基金
英国医学研究理事会;
关键词
Multiple myeloma; Macrophages; Therapeutics; Microenvironment; TUMOR-ASSOCIATED MACROPHAGES; BONE-MARROW MACROPHAGES; MONOCLONAL GAMMOPATHY; EXTRACELLULAR-MATRIX; CELL MIGRATION; CD47; BLOCKADE; ANGIOGENESIS; CANCER; PROGRESSION; PROLIFERATION;
D O I
10.1007/s10555-020-09943-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Macrophages are a vital component of the tumour microenvironment and crucial mediators of tumour progression. In the last decade, significant strides have been made in understanding the crucial functional roles played by macrophages in the development of the plasma cell (PC) malignancy, multiple myeloma (MM). Whilst the interaction between MM PC and stromal cells within the bone marrow (BM) microenvironment has been extensively studied, we are only just starting to appreciate the multifaceted roles played by macrophages in disease progression. Accumulating evidence demonstrates that macrophage infiltration is associated with poor overall survival in MM. Indeed, macrophages influence numerous pathways critical for the initiation and progression of MM, including homing of malignant cells to BM, tumour cell growth and survival, drug resistance, angiogenesis and immune suppression. As such, therapeutic strategies aimed at targeting macrophages within the BM niche have promise in the clinical setting. This review will discuss the functions elicited by macrophages throughout different stages of MM and provide a comprehensive evaluation of potential macrophage-targeted therapies.
引用
收藏
页码:273 / 284
页数:12
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