Chow Kin-Hoe, Park Hee Jung, George Joshy, Yamamoto Keiko, Gallup Andrew D, Graber Joel H, Chen Yuanxin, Jiang Wen, Steindler Dennis A, Neilson Eric G, Kim Betty Y S, Yun Kyuson
The Jackson Laboratory, Bar Harbor, Maine.
Department of Neurosurgery, Mayo Clinic, Jacksonville, Florida.
Cancer Res. 2017 Oct 1;77(19):5360-5373. doi: 10.1158/0008-5472.CAN-17-1294. Epub 2017 Aug 14.
Glioma stem cells (GSC) and epithelial-mesenchymal transition (EMT) are strongly associated with therapy resistance and tumor recurrence, but the underlying mechanisms are incompletely understood. Here, we show that S100A4 is a novel biomarker of GSCs. S100A4 cells in gliomas are enriched with cancer cells that have tumor-initiating and sphere-forming abilities, with the majority located in perivascular niches where GSCs are found. Selective ablation of S100A4-expressing cells was sufficient to block tumor growth and We also identified S100A4 as a critical regulator of GSC self-renewal in mouse and patient-derived glioma tumorspheres. In contrast with previous reports of S100A4 as a reporter of EMT, we discovered that S100A4 is an upstream regulator of the master EMT regulators and along with other mesenchymal transition regulators in glioblastoma. Overall, our results establish S100A4 as a central node in a molecular network that controls stemness and EMT in glioblastoma, suggesting S100A4 as a candidate therapeutic target. .
胶质瘤干细胞(GSC)与上皮-间质转化(EMT)与治疗抵抗和肿瘤复发密切相关,但其潜在机制尚未完全明确。在此,我们表明S100A4是GSC的一种新型生物标志物。胶质瘤中的S100A4细胞富含具有肿瘤起始和形成球体能力的癌细胞,其中大多数位于发现GSC的血管周围微环境中。选择性消融表达S100A4的细胞足以阻断肿瘤生长,并且我们还确定S100A4是小鼠和患者来源的胶质瘤肿瘤球中GSC自我更新的关键调节因子。与之前将S100A4作为EMT报告因子的报道相反,我们发现S100A4是EMT主要调节因子的上游调节因子,并且与胶质母细胞瘤中的其他间质转化调节因子一起。总体而言,我们的结果确立了S100A4作为控制胶质母细胞瘤干性和EMT的分子网络中的中心节点,表明S100A4作为候选治疗靶点。