Samei Lv, Yaling Pang, Lihua Yang, Yan Zhang, Shuyan Jiang
Department of Elderly Digestion, Shaanxi Provincial People's Hospital, Xi'an, Shaanxi, China (mainland).
Department of Ophthalmology, Shaanxi Provincial People's Hospital, Xi'an, Shaanxi, China (mainland).
Med Sci Monit. 2016 Nov 1;22:4126-4131. doi: 10.12659/msm.898152.
BACKGROUND This study investigated the effects and mechanism of imatinib in inhibiting colon cancer cell proliferation. MATERIAL AND METHODS The SW480 cells were divided into 4 imatinib-treated groups: 0 μM, 1.25 μM, 2.5 μM, and 5μM. We analyzed the apoptosis and cell cycle of the 4 groups. The gene and protein expressions of p21, p27, HGF, and GAPDH were measured by RT-PCR and Western blot. RESULTS Compared with the 0-μM imatinib-treated group, the apoptosis of 1.25-μM, 2.5-μM, and 5.0-μM treated groups was significantly induced (P<0.05, all). The G1 phase was significantly up-regulated in the 1.25-μM, 2.5-μM, and 5.0-μM treated groups compared with the 0-μM imatinib-treated group (P<0.05, respectively), but the S and G2 phase of 3 imatinib-treated groups were significantly down-regulated (P<0.05, all). The gene and protein expressions of p27 and HGF were significantly different among the 4 groups (P<0.05, all). CONCLUSIONS Imatinib inhibits proliferation of colon cancer cells by reducing HGF and increasing p27 in a dose-dependent manner.
背景 本研究探讨了伊马替尼抑制结肠癌细胞增殖的作用及机制。材料与方法 将SW480细胞分为4个伊马替尼处理组:0 μM、1.25 μM、2.5 μM和5 μM。我们分析了这4组细胞的凋亡和细胞周期。通过RT-PCR和蛋白质印迹法检测p21、p27、HGF和GAPDH的基因和蛋白表达。结果 与0 μM伊马替尼处理组相比,1.25 μM、2.5 μM和5.0 μM处理组的凋亡明显诱导(均P<0.05)。与0 μM伊马替尼处理组相比,1.25 μM、2.5 μM和5.0 μM处理组的G1期明显上调(分别P<0.05),但3个伊马替尼处理组的S期和G2期明显下调(均P<0.05)。4组之间p27和HGF的基因和蛋白表达有显著差异(均P<0.05)。结论 伊马替尼通过以剂量依赖的方式降低HGF和增加p27来抑制结肠癌细胞的增殖。