Annexin II interactions with the annexin II receptor enhance multiple myeloma cell adhesion and growth in the bone marrow microenvironment

被引:60
作者
D'Souza, Sonia
Kurihara, Noriyoshi
Shiozawa, Yusuke [2 ]
Joseph, Jeena [2 ]
Taichman, Russell [2 ]
Galson, Deborah L.
Roodman, G. David [1 ]
机构
[1] Univ Pittsburgh, Sch Med, UPMC,Div Hematol Oncol & Bone, VA Healthcare Syst,Univ Dr C,Med Ctr,Dept Med,Bio, Pittsburgh, PA 15240 USA
[2] Univ Michigan, Sch Dent, Dept Periodont & Oral Med, Ann Arbor, MI 48109 USA
基金
美国国家卫生研究院;
关键词
INCREASES OSTEOCLAST FORMATION; BINDING PROTEINS; EXPRESSION; THERAPY; BIOLOGY; CLONING;
D O I
10.1182/blood-2011-11-393348
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Multiple myeloma (MM) is an incurable B-cell malignancy in which the marrow microenvironment plays a critical role in our inability to cure MM. Marrow stromal cells in the microenvironment support homing, lodging, and growth of MM cells through activation of multiple signaling pathways in both MM and stromal cells. Recently, we identified annexin II (AXII) as a previously unknown factor produced by stromal cells and osteoclasts (OCL) that is involved in OCL formation, HSC and prostate cancer (PCa) homing to the BM as well as mobilization of HSC and PCa cells. AXII expressed on stromal cells supports PCa cell lodgment via the AXII receptor (AXIIR) on PCa cells, but the role of AXII and AXIIR in MM is unknown. In this study, we show that MM cells express AXIIR, that stromal/osteoblast-derived AXII facilitates adhesion of MM cells to stromal cells via AXIIR, and OCL-derived AXII enhances MM cell growth. Finally, we demonstrate that AXII activates the ERK1/2 and AKT pathways in MM cells to enhance MM cell growth. These results demonstrate that AXII and AXIIR play important roles in MM and that targeting the AXII/AXIIR axis may be a novel therapeutic approach for MM. (Blood. 2012; 119(8):1888-1896)
引用
收藏
页码:1888 / 1896
页数:9
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