扁桃体间充质干细胞的条件培养基对实体癌细胞显示出不同的细胞毒性率

M. Yüce, Esra Albayrak, Çağrı Gümüşkaptan
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引用次数: 0

摘要

目的:间充质干细胞(MSCs)是癌症研究的热点。有研究表明,间充质干细胞分泌的因子,尤其是间充质干细胞释放的因子,对肿瘤的发展具有抗肿瘤或抑制肿瘤的作用。不同来源的间充质干细胞表现出不同的抗肿瘤作用,而同一来源的间充质干细胞对不同癌细胞也表现出不同的抗肿瘤作用。在此,我们研究了作为间充质干细胞新来源的腭扁桃体间充质干细胞(TMSC)分泌的可溶性因子对人肺癌(A549)和胰腺癌(PANC-1)细胞系的抗肿瘤作用。 研究方法从腭扁桃体组织中分离出的TMSCs获得了条件培养基(CM),并通过MTT分析证实了CM对A549和PANC-1细胞生长的细胞毒性作用呈剂量依赖性。此外,通过碘化丙啶(PI)细胞周期分析法和流式细胞术检测Annexin-V/PI法,分别研究了CM处理对癌细胞细胞周期状态和凋亡过程的作用。 结果结果表明,TMSC-CM 处理 48 小时后可明显降低 A549 和 PANC-1 细胞株的存活率,且呈剂量依赖性。此外,TMSC-CM 还能诱导 A549 和 PANC-1 细胞凋亡,并使细胞停滞于 G2/M。 结论鉴于这些发现,我们的研究首次表明,TMSC-CM 通过刺激 A549 和 PANC-1 细胞凋亡具有抗肿瘤作用。这些发现揭示了中药具有无细胞治疗潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Conditioned media of tonsil derived mesenchymal stem cells shows different rates of cytotoxicity on solid cancer cells
Aims: Mesenchymal stem cells (MSCs) are the apple of the eye of cancer studies. It was indicated that the secreted factors, especially released by MSCs, have tumoral or anti-tumoral effects on tumor progression. MSCs obtained from different sources show different anti-tumoral effects, while MSCs originating from the same source also show different tumoral effects in different cancer cells. Here, we investigated the anti-tumor effects of soluble factors secreted from palatine tonsil MSCs (TMSC) as a new source of MSC on human lung carcinoma (A549) and pancreatic cancer (PANC-1) cell lines. Methods: Conditioned medium (CM) was obtained from TMSCs isolated from palatine tonsil tissue, and the cytotoxic effect of CM on the growth of A549 and PANC-1 in a dose-dependent manner was demonstrated by MTT analysis. In addition, the function of CM treatment on the cell cycle status of cancer cells and the apoptosis process were investigated through cell cycle analysis with propidium iodide (PI) and Annexin-V/PI detection method by flow cytometry analysis, respectively. Results: We demonstrated that TMSC-CM treatment significantly decreased the viability of A549 and PANC-1 cell lines in a dose-dependent manner post-48 hours. In addition, CM treatment differentially induced the apoptosis on A549 and PANC-1 cells and also, caused G2/M arrest in the cells. Conclusion: In light of these findings, our study is the first to show that TMSC-CM has an anti-tumoral effect by stimulating apoptosis on A549 and PANC-1 cells. These findings reveal that the usage of CM has a cell-free cellular therapeutic potential.
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