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Off-target effect of the BMI1 inhibitor PTC596 drives epithelial-mesenchymal transition in glioblastoma multiforme

机译:BMI1抑制剂PTC596的脱靶作用驱动多形性胶质母细胞瘤中的上皮-间质转化

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摘要

Representative images of GBM0811 cells treated for 6 days by DMSO, PTC596 (5 and 50 nM), and A1016 (5 and 50 nM). Scale bar: 2.5 mm. Quantification of cell viability in GBM0811 cells treated for 6 days by DMSO, PTC596 (5 and 50 nM) and A1016 (5 and 50 nM). GBM1205 cell growth assay upon acute treatment (7 days) with BMI1 inhibitors PTC596 and A1016. Top: scheme of the assay. Bottom: representative images at each time point. Scale bar: 2.5 mm. Size distribution of the spheres at day 50 from experiment in after PTC596 or A1016 treatments in comparison to DMSO-treated cells. Colony-forming assay after acute treatment (2 days) with BMI1 inhibitors and two passages of the GBM0410 cells. Top: scheme of the assay. Bottom: representative images at each time point. Scale bar: 2.5 mm. Quantification of the number of spheres after one and two passages in PTC596 (Top) or A1016 (Bottom) treated cells.
机译:DMSO,PTC596(5和50µnM)和A1016(5和50µnM)处理6天的GBM0811细胞的代表性图像。比例尺:2.5mm。用DMSO,PTC596(5和50nM)和A1016(5和50nM)处理6天的GBM0811细胞中的细胞活力定量。使用BMI1抑制剂PTC596和A1016进行急性治疗(7天)后进行GBM1205细胞生长测定。上:检测方案。下:每个时间点的代表性图像。比例尺:2.5mm。与DMSO处理的细胞相比,PTC596或A1016处理后第50天实验的球体尺寸分布。急性治疗(2天)后,用BMI1抑制剂和两次传代的GBM0410细胞进行菌落形成试验。上:检测方案。下:每个时间点的代表性图像。比例尺:2.5mm。量化PTC596(顶部)或A1016(底部)处理过的细胞经过一和两次传代后球体的数量。

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