布洛芬通过PI3K/Akt/mTOR信号通路对肉瘤细胞增殖和凋亡的影响

Ye Bai, Ning Guo, Qinghe Chen, Yuxi Chen, Zhenggang Bi
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引用次数: 4

摘要

目前国内对肉瘤细胞增值性凋亡的研究严重缺乏。特别是在临床医学中,探索布洛芬在PI3K/Akt/mTOR信号通路下对纤维肉瘤细胞生长和凋亡的影响,不仅可以有效地提前预防,而且是突破这一领域的一个很好的途径。本研究的主要目的是探讨布洛芬通过PI3K/Akt/mTOR信号通路对纤维肉瘤细胞增殖、细胞周期和凋亡的影响。我们将HTl080细胞系分为零对照组、对照组和实验组。萎凋组不接种任何细胞,对照组只添加等量的培养基,实验组分别添加5、10、15、20浓度的培养基。我们发现,对照组肉瘤细胞的凋亡率从5.66%上升到7.12%,而实验组肉瘤细胞的凋亡率上升明显快于对照组,整体上升7.16%,从4.56%上升到11.72%。因此,我们可以肯定,布洛芬在PI3K/Akt/mTOR信号通路下对纤维肉瘤细胞的增殖、细胞周期和凋亡具有很好的抑制作用。因此,当布洛芬注入体内时,不仅可以很好地观察肉瘤细胞,还可以在PI3K/Akt/mTOR信号通路下反映布洛芬对体内其他物质的良好抑制作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ibuprofen on Proliferation and Apoptosis of Sarcoma Cells via PI3K/Akt/mTOR Signaling Pathway.

Nowadays, there is a serious lack of information about the value-added apoptosis of sarcoma cells in China. Especially in clinical medicine, exploring the effect of ibuprofen on the growth and apoptosis of fibrosarcoma cells under the PI3K/Akt/mTOR signaling pathway can not only effectively prevent us in advance, but also be a great way to break through this field. The main purpose of this study was to investigate the effects of ibuprofen on the proliferation, cell cycle and apoptosis of fibrosarcoma cells through the PI3K/Akt/mTOR signaling pathway. We divided the HTl080 cell line into zero control group, control group and experimental group. The withering group was not inoculated with any cells, while the control group was only added with the same amount of culture medium, while the experimental group was added with 5,10,15,20 concentrations respectively. We found that the apoptosis rate of sarcoma cells in the control group increased from 5.66% to 7.12%, while the apoptosis rate of sarcoma cells in the experimental group increased significantly faster than that in the control group, with an overall increase of 7.16%, from 4.56% to 11.72%. Therefore, we can be surer that ibuprofen has a very good inhibitory effect on the proliferation, cell cycle and apoptosis of fibrosarcoma cells under the PI3K/Akt/mTOR signaling pathway. Therefore, when ibuprofen was injected into the body, it could not only observe the sarcoma cells well but also reflect the good inhibitory effect of ibuprofen on other substances in vivo under the PI3K/Akt/mTOR signaling pathway.

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