Peng Changliang, Zhao Hui, Chen Wei, Song Yan, Wang Xiaoying, Li Ji, Qiao Yong, Wu Dongjin, Ma Shengzhong, Wang Xiuwen, Gao Chunzheng
Department of Orthopaedics, Shandong University Second Hospital, Jinan, China.
Department of Orthopaedics, Beijing Chaoyang Hospital, Capital Medical University, Beijing, China.
Oncotarget. 2016 Oct 11;7(41):66822-66834. doi: 10.18632/oncotarget.11651.
The SS18-SSX1 fusion gene has been shown to play important roles in the development of synovial sarcoma (SS), but the underlying molecular mechanisms and its downstream target genes are still not clear. Here SHC SH2-domain binding protein 1 (SHCBP1) was identified and validated to be a novel downstream target gene of SS18-SSX1 by using microarray assay, quantitative real-time (qPCR) and western blot. Expression of SHCBP1 was firstly confirmed in SS cell line and SS tissues. The effects of SHCBP1 overexpression or knockdown on SS cell proliferation and tumorigenicity were then studied by cell proliferation, DNA replication, colony formation, flow cytometric assays, and its in vivo tumorigenesis was determined in the nude mice. Meanwhile, the related signaling pathways of SHCBP1 were also examined in SS cells. The results indicated that SHCBP1 was significantly increased in SS cells and SS tissues compared with adjacent noncancerous tissues. The expression of SHCBP1 was demonstrated to be positively correlated with the SS18-SSX1 level. Overexpression and ablation of SHCBP1 promoted and inhibited, respectively, the proliferation and tumorigenicity of SS cells in vitro. SHCBP1 knockdown also significantly inhibited SS cell growth in nude mice, and lowered the MAPK/ERK and PI3K/AKT/mTOR signaling pathways and cyclin D1 expression. Our findings disclose that SHCBP1 is a novel downstream target gene of SS18-SSX1, and demonstrate that the oncogene SS18-SSX1 promotes tumorigenesis by increasing the expression of SHCBP1, which normally acts as a tumor promoting factor.
SS18 - SSX1融合基因已被证明在滑膜肉瘤(SS)的发生发展中起重要作用,但其潜在的分子机制及其下游靶基因仍不清楚。在此,通过微阵列分析、定量实时(qPCR)和蛋白质印迹法,鉴定并验证了SHC SH2结构域结合蛋白1(SHCBP1)是SS18 - SSX1的一个新的下游靶基因。首先在SS细胞系和SS组织中证实了SHCBP1的表达。然后通过细胞增殖、DNA复制、集落形成、流式细胞术分析研究了SHCBP1过表达或敲低对SS细胞增殖和致瘤性的影响,并在裸鼠中测定了其体内致瘤性。同时,也在SS细胞中检测了SHCBP1的相关信号通路。结果表明,与相邻非癌组织相比,SHCBP1在SS细胞和SS组织中显著升高。SHCBP1的表达与SS18 - SSX1水平呈正相关。SHCBP1的过表达和缺失分别促进和抑制了SS细胞在体外的增殖和致瘤性。SHCBP1敲低也显著抑制了裸鼠中SS细胞的生长,并降低了MAPK/ERK和PI3K/AKT/mTOR信号通路以及细胞周期蛋白D1的表达。我们的研究结果揭示了SHCBP1是SS18 - SSX1的一个新的下游靶基因,并表明癌基因SS18 - SSX1通过增加SHCBP1的表达促进肿瘤发生,而SHCBP1通常作为一种肿瘤促进因子发挥作用。