Radioimmunotherapy of human synovial sarcoma using a monoclonal antibody against FZD10

被引:66
作者
Fukukawa, Chikako [1 ]
Hanaoka, Hirofumi [2 ]
Nagayama, Satoshi [1 ]
Tsunoda, Tatsuhiko [3 ]
Toguchida, Junya [4 ]
Endo, Keigo [5 ]
Nakamura, Yusuke [1 ]
Katagiri, Toyomasa [1 ]
机构
[1] Univ Tokyo, Inst Med Sci, Ctr Human Genome, Mol Med Lab, Tokyo 1088639, Japan
[2] Gunma Univ, Grad Sch Med, Dept Bioimaging Informat Anal, Gunma 3718511, Japan
[3] RIKEN, SNP Res Ctr, Lab Med Informat, Yokohama, Kanagawa 2300045, Japan
[4] Kyoto Univ, Inst Frontier Med Sci, Kyoto 6068507, Japan
[5] Gunma Univ, Grad Sch Med, Dept Nucl Med & Diagnost Radiol, Gunma 3718511, Japan
来源
CANCER SCIENCE | 2008年 / 99卷 / 02期
关键词
D O I
10.1111/j.1349-7006.2007.00701.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We previously reported Frizzled homolog 10 (FZD10), a member of the Frizzled family, to be a promising therapeutic target for synovial sarcomas. In this report, we established a murine monoclonal antibody (MAb), namely, MAb 92-13 that had specific binding activity against native FZD10 product expressed in synovial sarcoma cell lines. Subsequent immunohistochemical analyses with the MAb 92-13 confirmed an absence or hardly detectable level of FZD10 protein in any normal human organs. We confirmed the specific binding activity of this MAb in vivo after injection of fluorescent-labeled MAb i.p. or i.v. into the mice carrying synovial sarcoma xenografts by the use of the in vivo fluorescent imaging system as well as radioisotopes. Moreover, MAb 92-13 was effectively internalized into the synovial sarcoma cells after its binding to FZD10 on the cell surface. A single i.v. injection of the Yttrium-90 (Y-90)-MAb 92-13 drastically suppressed tumor growth of synovial sarcoma in mice without any severe toxicity. Median time to tumor progression was 58 days for mice treated with Y-90-MAb 92-13 and 9 days for mice treated with non-labeled antibody control or untreated mice (difference = 49 days; P = 7 x 10(-5)). This result indicates that MAb 92-13 could be utilized as the novel treatment modality for synovial sarcoma and other FZD10-positive tumors.
引用
收藏
页码:432 / 440
页数:9
相关论文
共 16 条
[11]   Molecular cloning of Frizzled-10, a novel member of the Frizzled gene family [J].
Koike, J ;
Takagi, A ;
Miwa, T ;
Hirai, M ;
Terada, M ;
Katoh, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 262 (01) :39-43
[12]  
Maloney DG, 1997, BLOOD, V90, P2188
[13]   Therapeutic potential of antibodies against FZD10, a cell-surface protein, for synovial sarcomas [J].
Nagayama, S ;
Fukukawa, C ;
Katagiri, T ;
Okamoto, T ;
Aoyama, T ;
Oyaizu, N ;
Imamura, M ;
Toguchida, J ;
Nakamura, Y .
ONCOGENE, 2005, 24 (41) :6201-6212
[14]  
Nagayama S, 2002, CANCER RES, V62, P5859
[15]   Yttriutm-90 (90Y) ibritumomab tiuxetan (Zevalin®) induces long-term durable responses in patients with relapsed or refractory B-cell non-Hodgkin's lymphoma [J].
Wiseman, GA ;
Witzig, TE .
CANCER BIOTHERAPY AND RADIOPHARMACEUTICALS, 2005, 20 (02) :185-188
[16]   The histological response to chemotherapy as a predictor of the oncological outcome of operative treatment of Ewing sarcoma [J].
Wunder, JS ;
Paulian, G ;
Huvos, AG ;
Heller, G ;
Meyers, PA ;
Healey, JH .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 1998, 80A (07) :1020-1033