Kimura T, Wang L, Tabu K, Tsuda M, Tanino M, Maekawa A, Nishihara H, Hiraga H, Taga T, Oda Y, Tanaka S
Department of Translational Pathology, Hokkaido University Graduate School of Medicine, Sapporo, Japan.
Department of Stem Cell Regulation, Medical Research Institute, Tokyo Medical and Dental University (TMDU), Yushima, Bunkyo-ku, Tokyo, Japan.
Oncogene. 2016 Jul 28;35(30):3932-43. doi: 10.1038/onc.2015.461. Epub 2015 Dec 7.
Synovial sarcoma accounts for almost 10% of all soft tissue sarcomas, and its prognosis is poor with 5-year survival rates at 36%. Thus, new treatments and therapeutic targets for synovial sarcoma are required. Tumor-initiating cells have been defined by the ability for self-renewal and multipotent differentiation, and they exhibit higher tumorigenic capacity, chemoresistance and radiation resistance, expecting to be a new therapeutic target. In synovial sarcoma, the presence of such stemness remains largely unclear; thus, we analyzed whether synovial sarcoma possessed tumor-initiating cells and explored specific markers, and we discovered that synovial sarcoma cell lines possessed heterogeneity by way of containing a sphere-forming subpopulation highly expressing NANOG, OCT4 and SOX2. By expression microarray analysis, CXCR4 was identified to be highly expressed in the sphere subpopulation and correlated with stem-cell-associated markers. Inhibition of CXCR4 suppressed the cell proliferation of synovial sarcoma cell lines in vitro. The tumor-initiating ability of CXCR4-positive cells was demonstrated by xenograft propagation assay. CXCR4-positive cells showed higher tumorigenicity than negative ones and possessed both self-renewal and multipotent differentiation ability. Immunohistochemical analysis of 39 specimens of synovial sarcoma patients revealed that CXCR4 strongly correlated with poor prognosis of synovial sarcoma. Thus, we conclude that CXCR4 is the marker of synovial sarcoma-initiating cells, a new biomarker for prognosis and a new potential therapeutic target.
滑膜肉瘤占所有软组织肉瘤的近10%,其预后较差,5年生存率为36%。因此,需要针对滑膜肉瘤的新治疗方法和治疗靶点。肿瘤起始细胞已通过自我更新和多能分化能力得以定义,它们表现出更高的致瘤能力、化学抗性和辐射抗性,有望成为新的治疗靶点。在滑膜肉瘤中,这种干性的存在在很大程度上仍不清楚;因此,我们分析了滑膜肉瘤是否拥有肿瘤起始细胞并探索了特异性标志物,并且我们发现滑膜肉瘤细胞系通过包含一个高表达NANOG、OCT4和SOX2的成球亚群而具有异质性。通过表达微阵列分析,CXCR4被鉴定为在球亚群中高表达并与干细胞相关标志物相关。抑制CXCR4可在体外抑制滑膜肉瘤细胞系的细胞增殖。通过异种移植增殖试验证明了CXCR4阳性细胞的肿瘤起始能力。CXCR4阳性细胞比阴性细胞表现出更高的致瘤性,并具有自我更新和多能分化能力。对39例滑膜肉瘤患者标本的免疫组织化学分析显示,CXCR4与滑膜肉瘤的不良预后密切相关。因此,我们得出结论,CXCR4是滑膜肉瘤起始细胞的标志物、一种新的预后生物标志物和一个新的潜在治疗靶点。