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首页> 外文期刊>European review for medical and pharmacological sciences. >Study on the influence of metformin on castration-resistant prostate cancer PC-3 cell line biological behavior by its inhibition on PLCε gene-mediated Notch1/Hes and androgen receptor signaling pathway
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Study on the influence of metformin on castration-resistant prostate cancer PC-3 cell line biological behavior by its inhibition on PLCε gene-mediated Notch1/Hes and androgen receptor signaling pathway

机译:二甲双胍对PLCε基因介导的Notch1 / Hes和雄激素受体信号通路的抑制作用对去势抵抗前列腺癌PC-3细胞生物学行为的影响

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OBJECTIVE: To study the regulation of metformin on the biological behaviors of the castration-resistant prostate cancer (CRPC) PC-3 cell such as proliferation, invasion, apoptosis through influencing Notch1/Hes and androgen receptor (AR) signaling pathway activity by its inhibition on the expression of PLCε gene. MATERIALS AND METHODS: Human prostate cancer-3 (PC-3) cell line was divided into PC-3 cell line (group A), PC-3 cell line + metformin (10 mM) (group B), PC-3 cell line + metformin (20 mM) (group C), PLCε gene knockout cell line (group D), PLCε knockout cell line + metformin (10 mM)_ (group E) and PLCε knockout cell line + metformin (20 mM) (group F), which were respectively tested at 24 h, 48 h and 72 h, and five duplicate wells were set at each time point in each group. Western blot assay and RT-PCR assay were used to test the relative expressions of PLCε, Notch1, Hes, AR protein and mRNA; MTT assay was used to test the cell proliferation. Transwell chamber was used to test the invasion capability. The scratch test was used to test the migration capability and the flow cytometer was used to test cell apoptosis. RESULTS: The relative expressions of PLCε, Notch1, Hes, AR protein and mRNA in Group A were increased gradually with time, but those values in group B and group C were decreased gradually with time and also significantly lower than those in group A (p 0.05). The proliferation, invasion and migration capabilities of the cells in group A, group D, group E and group F were gradually increased with time, but those in group B and group C were rapidly decreased with time and also significantly lower than those in group A, group D, group E and group F (p<0.05) at each time point. The apoptosis rates of group B and group C were increased gradually with time, and there was no other significant change in each group (p<0.05). CONCLUSIONS: Metformin can regulate the biological behaviors of CRPC PC-3 cell line such as proliferation, invasion, migration and apoptosis through influencing Notch1/Hes and AR signaling pathway activity by its inhibition on the expression of PLCε gene.
机译:目的:研究二甲双胍通过抑制Notch1 / Hes和雄激素受体(AR)信号通路活性,对去势抵抗性前列腺癌(CRPC)PC-3细胞的生物学行为如增殖,侵袭,凋亡的调控。 PLCε基因的表达材料与方法:将人类前列腺癌3(PC-3)细胞系分为PC-3细胞系(A组),PC-3细胞系+二甲双胍(10 mM)(B组),PC-3细胞系+二甲双胍(20 mM)(C组),PLCε基因敲除细胞系(D组),PLCε基因敲除细胞系+二甲双胍(10 mM)_(E组)和PLCε基因敲除细胞系+二甲双胍(20 mM)(F组),分别在24小时,48小时和72小时进行测试,并在每组的每个时间点设置5个重复的孔。用蛋白质印迹法和RT-PCR法检测PLCε,Notch1,Hes,AR蛋白和mRNA的相对表达。使用MTT测定法测试细胞增殖。用Transwell室测试侵袭能力。使用刮擦测试来测试迁移能力,并且使用流式细胞仪来测试细胞凋亡。结果:A组PLCε,Notch1,Hes,AR蛋白和mRNA的相对表达随时间逐渐升高,但B组和C组的相对表达随时间逐渐降低,也明显低于A组(p 0.05)。 A组,D组,E组和F组细胞的增殖,侵袭和迁移能力随着时间的推移逐渐增加,但B组和C组的细胞随着时间的推移迅速降低,并且也明显低于A组。 ,D组,E组和F组在每个时间点(p <0.05)。 B组和C组的凋亡率均随时间逐渐增加,各组均无其他显着变化(p <0.05)。结论:二甲双胍可通过抑制Notch1 / Hes和AR信号通路的活性,从而抑制CRPC PC-3细胞的PLCε基因表达,从而调节其生物学行为,例如增殖,侵袭,迁移和凋亡。

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