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Mesenchymal stem cells administered in the early phase of tumorigenesis inhibit colorectal tumor development in rats

机译:在肿瘤发生早期给予的间充质干细胞抑制大鼠结直肠肿瘤的发展

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摘要

To investigate the differences between the effects of mesenchymal stem cells (MSCs) administered in the early and late phases of tumorigenesis, MSCs were isolated from bone marrow and colorectal tumors were produced by exposing 7-week-old F344 rats to 1,2-dimethylhydrazine and dextran sulfate sodium. We evaluated tumor number and volume (week 25), MSC localization, number of aberrant crypt foci (ACF), transforming growth factor (TGF)-β1 protein levels in the rectum after administration of MSCs (week 5 or 15), and the effects of MSC-conditioned medium on ACL15 cell proliferation. Administered MSCs labeled with PKH26 were observed in the rectum. Administered MSCs in the early phase (week 5) before tumor occurrence (week 12) significantly decreased tumor number and volume (1.5 vs 4 and 21 mm3 vs 170 mm3; p<0.01), but not administered MSCs in the late phase (week 15). Administered MSCs in the early phase reduced ACF number on days 14 and 35 (1.9 vs 4.1 and 3.7 vs 7.3; p<0.01). Rectal TGF-β1 increased 1.3 fold on day 3, and MSC-conditioned medium containing TGF-β1 abundantly inhibited ACL15 cell proliferation. MSCs administered in the early phase but not late phase inhibited colorectal tumor development in a rat model.
机译:为了研究在肿瘤发生的早期和晚期阶段施用的间充质干细胞(MSC)的作用之间的差异,从骨髓中分离MSC,并通过将7周大的F344大鼠暴露于1,2-二甲基肼来产生结直肠肿瘤和硫酸葡聚糖钠。我们评估了给予MSCs后(第5周或第15周)直肠中肿瘤的数量和体积(第25周),MSC定位,异常隐窝灶数(ACF),转化生长因子(TGF)-β1蛋白水平。条件培养基对ACL15细胞增殖的影响。在直肠中观察到用PKH26标记的施用的MSC。在肿瘤发生前(第12周)的早期(第5周)施用的MSC显着降低了肿瘤数量和体积(1.5对4和21mm 3 与170mm 3 ; p <0.01),但在晚期(第15周)未给予MSC。早期施用的MSC在第14天和第35天减少了ACF值(1.9对4.1和3.7对7.3; p <0.01)。直肠TGF-β1在第3天增加了1.3倍,并且含有TGF-β1的MSC条件培养基充分抑制了ACL15细胞的增殖。在大鼠模型的早期阶段而非晚期阶段施用的MSC抑制了结直肠肿瘤的发展。

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