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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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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)-beta 1 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 mm(3) vs 170 mm(3); 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-beta 1 increased 1.3 fold on day 3, and MSC-conditioned medium containing TGF-beta 1 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(MSCs)的作用之间的差异,从骨髓中分离MSCs,并将7周龄的F344大鼠暴露于1,2-二甲基肼后产生结直肠肿瘤和硫酸葡聚糖钠。我们评估了MSCs给药后直肠中的肿瘤数量和体积(第25周),MSC定位,异常隐窝病灶(ACF)数量,转化生长因子(TGF)-beta 1蛋白水平(第5周或第15周)以及条件培养基对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MSC显着降低了肿瘤数量和体积(1.5 vs 4和21 mm(3)vs 170 mm(3); p <0.01),但在后期(第15周)。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-beta 1在第3天增加了1.3倍,含有TGF-beta 1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给予的MSC抑制了结直肠肿瘤的发展。

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