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
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