Nagayama Satoshi, Fukukawa Chikako, Katagiri Toyomasa, Okamoto Takeshi, Aoyama Tomoki, Oyaizu Naoki, Imamura Masayuki, Toguchida Junya, Nakamura Yusuke
Laboratory of Molecular Medicine, Human Genome Center, The Institute of Medical Science, The University of Tokyo, Tokyo 108-8639, Japan.
Oncogene. 2005 Sep 15;24(41):6201-12. doi: 10.1038/sj.onc.1208780.
Genome-wide expression profiling revealed overexpression of the gene encoding frizzled homologue 10 (FZD 10), a cell-surface receptor for molecules in the Wnt pathway, as a potential contributor to synovial sarcomas (SS). Northern blotting and immunohistochemical staining confirmed that expression levels of FZD 10 were very high in nearly all SS tumors and cell lines examined but absent in most normal organs or in some cancers arising in other tissues. Treatment of human SS cells with small-interfering RNA (siRNA) to FZD 10 decreased the amount of its product and suppressed growth of SS cells. Moreover, a polyclonal antibody specifically recognizing the extracellular domain (ECD) of FZD 10 was markedly effective in mediating ADCC against FZD 10-overexpressing synovial sarcoma cells in vitro. Injection of the antibody into SS xenografts in nude mice attenuated tumor growth, and TUNEL assays revealed clusters of apoptotic cells in antibody-treated xenografts. Taken together, these findings suggest that a humanized antibody against FZD 10 might be a promising treatment for patients with tumors that overexpress FZD 10; minimal or no adverse reactions would be expected because FZD 10 protein is not abundant in vital organs.
全基因组表达谱分析显示,编码卷曲同源物10(FZD 10)的基因过表达,FZD 10是Wnt信号通路中分子的细胞表面受体,可能是滑膜肉瘤(SS)的一个促成因素。Northern印迹法和免疫组织化学染色证实,FZD 10的表达水平在几乎所有检测的SS肿瘤和细胞系中都非常高,但在大多数正常器官或其他组织发生的一些癌症中不存在。用针对FZD 10的小干扰RNA(siRNA)处理人SS细胞可减少其产物量并抑制SS细胞生长。此外,一种特异性识别FZD 10细胞外结构域(ECD)的多克隆抗体在体外介导针对过表达FZD 10的滑膜肉瘤细胞的ADCC方面非常有效。将该抗体注射到裸鼠的SS异种移植瘤中可减缓肿瘤生长,TUNEL分析显示抗体处理的异种移植瘤中有凋亡细胞簇。综上所述,这些发现表明,针对FZD 10的人源化抗体可能是过表达FZD 10的肿瘤患者的一种有前景的治疗方法;由于FZD 10蛋白在重要器官中不丰富,预计不良反应极小或无不良反应。