Bone Marrow Microenvironment and Tumor Progression

被引:48
作者
Chantrain, Christophe F. [1 ,2 ]
Feron, Olivier [3 ]
Marbaix, Etienne [2 ,4 ]
DeClerck, Yves A. [5 ,6 ,7 ]
机构
[1] Catholic Univ Louvain, Dept Pediat, Div Hematol Oncol, Brussels, Belgium
[2] Catholic Univ Louvain, Christian Duve Inst Cellular Pathol, Cell Biol Unit, Brussels, Belgium
[3] Catholic Univ Louvain, Unit Pharmacol & Therapeut, Brussels, Belgium
[4] Catholic Univ Louvain, Sch Med, Dept Pathol, Brussels, Belgium
[5] Univ Southern Calif, Keck Sch Med, Dept Pediat, Div Hematol Oncol, 4650 Sunset Blvd,MS 54, Los Angeles, CA 90033 USA
[6] Univ Southern Calif, Keck Sch Med, Dept Biochem & Mol Biol, Div Hematol Oncol, Los Angeles, CA 90033 USA
[7] Childrens Hosp Los Angeles, Saban Res Inst, Los Angeles, CA 90033 USA
关键词
Tumor microenvironment; Angiogenesis; Vasculogenesis; Metastasis; Bone marrow microenvironment; Bone marrow stem cells;
D O I
10.1007/s12307-008-0010-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The bone marrow constitutes an unique microenvironment for cancer cells in three specific aspects. First, the bone marrow actively recruits circulating tumor cells where they find a sanctuary rich in growth factors and cytokines that promote their proliferation and survival. When in the bone marrow, tumor cells profoundly affect the homeostasis of the bone and the balance between osteogenesis and osteolysis. As a consequence, growth and survival factors normally sequestered into the bone matrix are released, further fueling cancer progression. Second, tumor cells actively recruit bone marrow-derived precursor cells into their own microenvironment. When in the tumors, these bone marrow-derived cells contribute to an inflammatory reaction and to the formation of the tumor vasculature. Third, bone marrow-derived cells can home in distant organs, where they form niches that attract circulating tumor cells. Our understanding of the contribution of the bone marrow microenvironment to cancer progression has therefore dramatically improved over the last few years. The importance of this new knowledge cannot be underestimated considering that the vast majority of cancer treatments such as cytotoxic and myeloablative chemotherapy, bone marrow transplantation and radiation therapy inflict a trauma to the bone marrow microenvironment. How such trauma affects the influence that the bone marrow microenvironment exerts on cancer is still poorly understood. In this article, the reciprocal relationship between the bone marrow microenvironment and tumor cells is reviewed, and its potential impact on cancer therapy is discussed.
引用
收藏
页码:23 / 35
页数:13
相关论文
共 111 条
[1]   The inflammatory micro-environment in tumor progression: The role of tumor-associated macrophages [J].
Allavena, Paola ;
Sica, Antonio ;
Solinas, Graziella ;
Porta, Chiara ;
Mantovani, Alberto .
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2008, 66 (01) :1-9
[2]  
Anderson Kenneth C., 2000, Hematology Am Soc Hematol Educ Program, P147
[3]  
Ara T, 2008, CANC RES IN PRESS
[4]   Tie2/angiopoietin-1 signaling regulates hematopoietic stem cell quiescence in the bone marrow niche [J].
Arai, F ;
Hirao, A ;
Ohmura, M ;
Sato, H ;
Matsuoka, S ;
Takubo, K ;
Ito, K ;
Koh, GY ;
Suda, T .
CELL, 2004, 118 (02) :149-161
[5]   Maintenance of quiescent hematopoietic stem cells in the osteoblastic niche [J].
Arai, Fumio ;
Suda, Toshio .
HEMATOPOIETIC STEM CELLS VI, 2007, 1106 :41-53
[6]   Transplanted adult hematopoietic stems cells differentiate into functional endothelial cells [J].
Bailey, AS ;
Jiang, SG ;
Afentoulis, M ;
Baumann, CI ;
Schroeder, DA ;
Olson, SB ;
Wong, MH ;
Fleming, WH .
BLOOD, 2004, 103 (01) :13-19
[7]   Inflammation and cancer: back to Virchow? [J].
Balkwill, F ;
Mantovani, A .
LANCET, 2001, 357 (9255) :539-545
[8]   Cancer - An inflammatory link [J].
Balkwill, F ;
Coussens, LM .
NATURE, 2004, 431 (7007) :405-406
[9]   Matrix metalloproteinase-9 triggers the angiogenic switch during carcinogenesis [J].
Bergers, G ;
Brekken, R ;
McMahon, G ;
Vu, TH ;
Itoh, T ;
Tamaki, K ;
Tanzawa, K ;
Thorpe, P ;
Itohara, S ;
Werb, Z ;
Hanahan, D .
NATURE CELL BIOLOGY, 2000, 2 (10) :737-744
[10]  
Bertolini F, 2005, NEW ENGL J MED, V353, P2614