A clinically relevant SCID-hu in vivo model of human multiple myeloma

被引:97
作者
Tassone, P
Neri, P
Carrasco, DR
Burger, R
Goldmacher, VS
Fram, R
Munshi, V
Shammas, MA
Catley, L
Jacob, GS
Venuta, S
Anderson, KC
Munshi, NC
机构
[1] Dana Farber Canc Inst, Jerome Lipper Multiple Myeloma Ctr, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, VA Boston Healthcare Syst, Boston, MA USA
[3] Univ Magna Graecia, Catanzaro, Italy
[4] ImmunoGen Inc, Cambridge, MA USA
[5] Callisto Pharmaceut Inc, New York, NY USA
关键词
D O I
10.1182/blood-2005-01-0373
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We developed a novel in vivo multiple myeloma (MM) model by engrafting the interleukin 6 (IL-6)-dependent human MM cell line INA-6 into severe combined immunodeficiency (SCID) mice previously given implants of a human fetal bone chip (SCID-hu mice). INA-6 cells require either exogenous human IL-6 (huIL-6) or bone marrow stromal cells (BMSCs) to proliferate in vitro. In this model, we monitored the in vivo growth of INA-6 cells stably transduced with a green fluorescent protein (GFP) gene (INA-6(GFP+) cells). INA-6 MM cells engrafted in SCID-hu mice but not in SCID mice that had not been given implants of human fetal bone. The level of soluble human IL-6 receptor (shuIL-6R) in murine serum and fluorescence imaging of host animals were sensitive indicators of tumor growth. Dexamethasone as well as experimental drugs, such as Atiprimod and B-B4-DM1, were used to confirm the utility of the model for evaluation of anti-MM agents. We report that this model is highly reproducible and allows for evaluation of investigational drugs targeting IL-6-dependent MM cells in the human bone marrow (huBM) milieu.
引用
收藏
页码:713 / 716
页数:4
相关论文
共 22 条
[1]  
AKKINA RK, 1994, BLOOD, V84, P1393
[2]   Development of an in vivo model of human multiple myeloma bone disease [J].
Alsina, M ;
Boyce, B ;
Devlin, RD ;
Anderson, JL ;
Craig, F ;
Mundy, GR ;
Roodman, GD .
BLOOD, 1996, 87 (04) :1495-1501
[3]   Moving disease biology from the lab to the clinic [J].
Anderson, KC .
CANCER, 2003, 97 (03) :796-801
[4]   Targeted therapy for multiple myeloma [J].
Anderson, KC .
SEMINARS IN HEMATOLOGY, 2001, 38 (03) :286-294
[5]  
Burger R, 2001, Hematol J, V2, P42, DOI 10.1038/sj.thj.6200075
[6]   ENGRAFTMENT OF HUMAN HEMATOPOIETIC PRECURSOR CELLS WITH SECONDARY TRANSFER POTENTIAL IN SCID-HU MICE [J].
CHEN, BP ;
GALY, A ;
KYOIZUMI, S ;
NAMIKAWA, R ;
SCARBOROUGH, J ;
WEBB, S ;
FORD, B ;
CEN, DZ ;
CHEN, SC .
BLOOD, 1994, 84 (08) :2497-2505
[7]   Azaspirane (N-N-diethyl-8,8-dipropyl-2-azaspiro [4.5] decane-2-propanamine) inhibits human multiple myeloma cell growth in the bone marrow milieu in vitro and in vivo [J].
Hamasaki, M ;
Hideshima, T ;
Tassone, P ;
Neri, P ;
Ishitsuka, K ;
Yasui, H ;
Shiraishi, N ;
Raje, N ;
Kumar, S ;
Picker, DH ;
Jacob, GS ;
Richardson, PG ;
Munshi, NC ;
Anderson, KC .
BLOOD, 2005, 105 (11) :4470-4476
[8]   Molecular mechanisms of novel therapeutic approaches for multiple myeloma [J].
Hideshima, T ;
Anderson, KC .
NATURE REVIEWS CANCER, 2002, 2 (12) :927-937
[9]   The IL-6 receptor antagonist SANT-7 overcomes bone marrow stromal cell-mediated drug resistance of multiple myeloma cells [J].
Hönemann, D ;
Chatterjee, M ;
Savino, R ;
Bommert, K ;
Burger, R ;
Gramatzki, M ;
Dörken, B ;
Bargou, RC .
INTERNATIONAL JOURNAL OF CANCER, 2001, 93 (05) :674-680
[10]  
HUANG YW, 1993, CANCER RES, V53, P1392