锂、二甲双胍和依维莫司对二维和三维石川子宫内膜癌细胞培养中细胞生长的影响

Emine Tural, N. Çil, Mücahit Seçme, Gülçin Abban Mete, Hakan Darici, Ayhan Bilir, E. Karaoz
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引用次数: 0

摘要

目的:我们的目的是研究艾维莫司、二甲双胍和氯化锂在二维(2D,单层)和三维(3D,球形)石川细胞(由子宫内膜癌细胞系组成)细胞培养中的单一和联合治疗效果。材料和方法作为研究的一部分,研究人员测定了单一或联合使用依维莫司、二甲双胍和氯化锂对细胞活力、侵袭、集落形成和凋亡以及 PI3K/AKT/mTOR 通路的影响。细胞活力采用 XTT 法进行评估。用 RT-PCR 评估 CASP3、CASP8、CASP9、FASL、FADD、TNF、TRADD、BAX、P53、PI3KCA、PI3KCB、PTEN、MTOR、AKT1 基因,用流式细胞术评估细胞凋亡,用倒置显微镜分析评估三维球形结果。结果48小时后,依维莫司、二甲双胍和锂的IC50水平分别为37.46 nM、48.59 mM和100 µM。实验结果表明,处理组中石川细胞的侵袭能力和细胞集落形成均显著降低。此外,与对照组相比,石川球形细胞也明显受到抑制。RT-PCR 结果显示,这些物质及其组合会影响与 PI3K/AKT/mTOR 通路和细胞凋亡相关的基因。流式细胞术结果表明,单药和联合用药可明显增加细胞凋亡。结论因此,依维莫司、二甲双胍和锂的单药和复方制剂通过各种机制减少了石川细胞的细胞增殖、诱导细胞凋亡并降低了 mTOR 的激活。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Effects of Lithium, Metformin and Everolimus Substances on Cell Growth in 2D and 3D Ishikawa Endometrial Carcinoma Cell Culture
Purpose: Our aim is to study the effects of the single and combined treatments of Everolimus, Metformin, and Lithium Chloride in two-dimensional (2D, monolayer) and three-dimensional (3D, spheroid) cell cultures of Ishikawa cells, which comprise the endometrial cancer cell line. Materials and methods: As part of the study, the effects of single and combined forms of Everolimus, Metformin, and Lithium Chloride were determined on cell viability, invasion, colony formation and apoptosis, and PI3K/AKT/mTOR pathway. Cell viability was assessed using XTT assay. CASP3, CASP8, CASP9, FASL, FADD, TNF, TRADD, BAX, P53, PI3KCA, PI3KCB, PTEN, MTOR, AKT1 genes were evaluated with RT-PCR, apoptosis was evaluated by flow cytometry and 3D spheroid results were evaluated with invert microscope analysis. Results: Everolimus, metformin, and lithium's IC50 levels were found at 48 hours to be 37.46 nM, 48.59 mM, and 100 µM, respectively. It was determined that the invasive capacities of Ishikawa cells in treatment groups, as well as cell colony formation were significantly reduced. In addition, Ishikawa spheroid cells were significantly suppressed compared with the control groups. RT-PCR results revealed that substances and their combinations affect genes associated with PI3K/AKT/mTOR pathway and apoptosis. Flow cytometry results showed notably increased apoptosis by single and combined treatments. Conclusion: As a result, the single and combination forms of everolimus, metformin, and lithium have reduced cell proliferation, induced apoptosis, and decreased mTOR activation through various mechanisms in Ishikawa cells.
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