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Ang-2 promoting proliferation of SW1116 colon cancer cells through PI3K/Akt pathways

机译:Ang-2通过PI3K / Akt途径促进SW1116结肠癌细胞的增殖

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To investigate the role of the angiopoietin-2 (Ang-2) signal transduction pathway in colon cancer, colon cancer cells (SW1116) were divided into four groups, control group, serum-free group, Ang-2 group (treated with 1.2 mg/L Ang-2) and PI3K/Akt inhibitor group (treated with LY294002 and Ang-2). Then Tie-2, PI3K and Akt were detected via Western blotting after 24 h. Compared to the serum-free group, the expression of Tie-2 and Akt in the Ang-2 group was increased (p=0.294, p>0.05; p=0.00, p<0.01), while the expression of PI3K was decreased significantly in the Ang-2 group (p=0.00, p<0.01). Compared to the Ang-2 group, the expression of all three of the proteins was decreased significantly in the inhibitor LY294002 group (p = 0.00, p<0.01; p=0.00, p<0.01; p=0.00, p<0.01). Ang-2 plays an important role in the proliferation of colon cancer cells, which can be inhibited by LY294002, and the PI3K/Akt pathway may take part in the inhibition mechanism.
机译:为了研究血管生成素2(Ang-2)信号转导通路在结肠癌中的作用,将结肠癌细胞(SW1116)分为四组,对照组,无血清组,Ang-2组(用1.2 mg处理) / L Ang-2)和PI3K / Akt抑制剂组(用LY294002和Ang-2处理)。然后在24小时后通过蛋白质印迹法检测Tie-2,PI3K和Akt。与无血清组相比,Ang-2组中Tie-2和Akt的表达增加(p = 0.294,p> 0.05; p = 0.00,p <0.01),而PI3K的表达则明显降低。在Ang-2组中(p = 0.00,p <0.01)。与Ang-2组相比,抑制剂LY294002组中所有三种蛋白质的表达均显着降低(p = 0.00,p <0.01; p = 0.00,p <0.01; p = 0.00,p <0.01)。 Ang-2在结肠癌细胞的增殖中起重要作用,其可以被LY294002抑制,PI3K / Akt途径可能参与了其抑制机制。

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