摘要
目的:在构建沉默RORα人胃癌MGC803细胞的基础上,观察沉默RORα对MGC803细胞增殖与迁移侵袭的影响。方法:软琼脂集落形成实验、流式细胞术、细胞迁移和侵袭实验检测RORα沉默对MGC803细胞增殖、细胞周期、迁移和侵袭能力的影响。RT-PCR与Western blot检测RORα、Wnt1、MMP-9与TIMP3 m RNA与蛋白表达。结果:集落形成实验显示,沉默组的集落形成率128.1%明显高于对照组和空载体组(P<0.05)。流式细胞术显示,沉默组S期细胞百分率39.9%较对照组26.1%和空载体组27.4%明显增加(P<0.05)。迁移实验显示,沉默组迁移距离(1.76±0.19)mm明显高于对照组(1.32±0.14)mm和空载体组(1.29±0.17)mm(P<0.05)。侵袭实验显示,沉默组穿膜细胞(172±27)个明显多于对照组(147±17)个和空载体组(149±14)个(P<0.05)。RT-PCR与Western blot表明,沉默RORα可显著上调Wnt1与MMP-9 m RNA与蛋白与下调RORα与TIMP3 m RNA与蛋白。结论:沉默RORα可通过Wnt信号通路上调MMP-9和下调TIMP3促进MGC803细胞增殖与迁移侵袭。
Objective:To investigate Silencing RORαthrough Wnt signaling pathway promote proliferation, migration and invasion in human gastric MGC803 cells underlaying construction of MGC803 cells of silencing RORα. Methods:Colony formation and lfow cytometry were used for cell proliferation and cell cycle. Wound healing and transwell assays were performed to examine cell migration and invasion activities. hTe expression of RORα, Wnt1, MMP-9 and TIMP3 mRNA and protein were detected by Western blot and RT-PCR. Results:hTe colony forming showed that the colony forming efficiency in miR-RORα group was 128.1% higher significantly than in control and vector/ MGC803 (P〈0.05). The flow cytometry revealed that percentage in S cycle was 39.9% in miR-RORα markedly increase than 26.1% in control and 27.4% in vector/MGC803 (P〈0.05). The migration experiment disclosed that migration distance in miR-RORα was (1.76±0.19) mm notably increase than (1.32±0.14) mm in control and (1.29±0.17) mm in vector/MGC803 (P〈0.05). The invasion essay exhibited that the cells of passed through the Matrigel were (172±27) in miR-RORα increased than (147±17) in control and (149±14) in vector/MGC803, respectively (P〈0.05). RT-PCR and Western blot indicated that silencing RORα up-regulated expression of wnt1 and MMP-9 and down-regulated expression of RORα and TIMP3, compared with control and vector/MGC803, respectively (P〈0.05). Conclusion: Silencing RORα can promote proliferation, migration and invasion through Wnt signaling pathway in human gastric MGC803 cells.
出处
《临床与病理杂志》
2016年第10期1562-1568,共7页
Journal of Clinical and Pathological Research
基金
国家自然基金(81374013)
湖南省卫计委科研课题(B2015-182)~~