Department of Biology, Osaka Medical Center for Cancer and Cardiovascular Diseases, Higashinari-ku, Osaka 537-8511, Japan.
Int J Oncol. 2010 Apr;36(4):823-31. doi: 10.3892/ijo_00000559.
Synovial sarcoma (SS) is an aggressive soft-tissue malignancy characterized by a unique t(X;18) translocation resulting in expression of SS18-SSX fusion protein. In order to investigate the biological function of this fusion protein and to develop a novel therapeutic option, we examined downregulation of SS18-SSX1 expression by small interfering RNA targeting SS18-SSX1 in three human SS cell lines. Microarray analysis comparing SS18-SSX1-silenced cells with control cells in three SS cell lines showed that SS18-SSX1 mainly affected the focal adhesion pathway. In accord with the array data, silencing of SS18-SSX1 enhances adhesion to the extracellular matrix through the induction of expression of myosin light-chain kinase. Furthermore, the silencing of SS18-SSX1 inhibits anchorage-independent growth in vitro and systemic delivery of siRNA against SS18-SSX1 using a nanoparticle system inhibited tumor growth in a nude mouse xenograft model. Our results demonstrate that siRNA targeting of SS18-SSX1 has therapeutic potential for the treatment of SS.
滑膜肉瘤(SS)是一种侵袭性软组织恶性肿瘤,其特征在于存在独特的 t(X;18)易位,导致 SS18-SSX 融合蛋白的表达。为了研究该融合蛋白的生物学功能并开发新的治疗方法,我们通过针对 SS18-SSX1 的小干扰 RNA 下调了三种人 SS 细胞系中的 SS18-SSX1 表达。在三种 SS 细胞系中比较 SS18-SSX1 沉默细胞与对照细胞的微阵列分析表明,SS18-SSX1 主要影响粘着斑途径。与数组数据一致,通过诱导肌球蛋白轻链激酶的表达,SS18-SSX1 的沉默增强了对细胞外基质的黏附。此外,SS18-SSX1 的沉默抑制了体外无锚定生长,并且使用纳米颗粒系统体内递送针对 SS18-SSX1 的 siRNA 抑制了裸鼠异种移植模型中的肿瘤生长。我们的研究结果表明,针对 SS18-SSX1 的 siRNA 具有治疗 SS 的潜力。