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Human Stromal Cells in the Peripheral Zone of the Prostate Promote Tumorigenesis of Prostatic Cancer Stem Cells through Up-regulation of C-Kit Expression

机译:前列腺周围区域的人类基质细胞通过上调C-Kit表达促进前列腺癌干细胞的肿瘤发生

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摘要

>Objective: Most prostate cancers originate from the prostatic peripheral zone (PZ). We tested the hypothesis that the stromal cells from PZ and transitional zone (TZ) have differential effects on the ability of tumorigenesis.>Methods: Stromal cells isolated from the PZ and TZ of normal human prostates mixed with DU145 cells subcutaneously injected into athymic nude mice. The volume and weight of tumors was measured and analyzing the ability of purified DU145 cells isolated from the tumors to migrate and proliferate. The expression patterns of stem cell-specific genes of these DU145 cells were examined. The C-Kit inhibitor, imatinib mesylate, was administrated to confirm the effect of stromal cells on the tumorigenesis.>Results: The volume and weight of tumors were significantly higher in mice transplanted with DU145 and stromal cells from PZ. In contrast, the data was significantly lower with DU145 and stromal cells from TZ than DU145 alone. The purified DU145 cells isolated from the tumors with DU145 and stromal cells in PZ had increased ability to migrate and proliferate, and had increased expression of C-Kit. These effects of the stromal cells in the PZ on DU145 cells could be blocked using imatinib mesylate.>Conclusions: Human stromal cells in the PZ promote the in vivo tumorigenesis of DU145 through up-regulating C-Kit; in contrast, the stromal cells in the TZ inhibit it through down-regulating the expression of C-Kit. The model will be useful for understanding the mechanisms by which the prostatic stem cell niche controls the tumorigeneis of prostatic cancer stem cells.
机译:>目标:大多数前列腺癌均起源于前列腺周围区域(PZ)。我们测试了以下假设:来自PZ和过渡区(TZ)的基质细胞对肿瘤发生能力具有不同的影响。>方法:从正常人前列腺的PZ和TZ中分离出的基质细胞与DU145细胞混合皮下注射到无胸腺裸鼠中。测量肿瘤的体积和重量,并分析从肿瘤分离的纯化的DU145细胞迁移和增殖的能力。检查了这些DU145细胞的干细胞特异性基因的表达模式。给予C-Kit抑制剂甲磺酸伊马替尼以确认基质细胞对肿瘤发生的作用。>结果:移植DU145和PZ基质细胞的小鼠的肿瘤体积和重量明显更高。相反,来自TZ的DU145和基质细胞的数据明显低于单独的DU145。从带有DU145的肿瘤中分离出的纯化的DU145细胞和PZ中的基质细胞具有增强的迁移和增殖能力,并具有增加的C-Kit表达。甲磺酸伊马替尼可阻断PZ基质细胞对DU145细胞的这些作用。>结论: PZ中的人类基质细胞通过上调C-Kit促进DU145的体内肿瘤发生。相反,TZ中的基质细胞通过下调C-Kit的表达来抑制它。该模型将有助于理解前列腺干细胞生态位控制前列腺癌干细胞肿瘤发生的机制。

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