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Determining Conditions for Successful Culture of Multi-Cellular 3D Tumour Spheroids to Investigate the Effect of Mesenchymal Stem Cells on Breast Cancer Cell Invasiveness

机译:成功培养多细胞3D肿瘤球状体的确定条件研究间充质干细胞对乳腺癌细胞侵袭的影响

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摘要

Mesenchymal stem cells have been widely implicated in tumour development and metastases. Moving from the use of two-dimensional (2D) models to three-dimensional (3D) to investigate this relationship is critical to facilitate more applicable and relevant research on the tumour microenvironment. We investigated the effects of altering glucose concentration and the source of foetal bovine serum (FBS) on the growth of two breast cancer cell lines (T47D and MDA-MB-231) and human bone marrow-derived mesenchymal stem cells (hBM-MSCs) to determine successful conditions to enable their co-culture in 3D tumour spheroid models. Subsequently, these 3D multi-cellular tumour spheroids were used to investigate the effect of hBM-MSCs on breast cancer cell invasiveness. Findings presented herein show that serum source had a statistically significant effect on two thirds of the growth parameters measured across all three cell lines, whereas glucose only had a statistically significant effect on 6%. It was determined that the optimum growth media composition for the co-culture of 3D hBM-MSCs and breast cancer cell line spheroids was 1 g/L glucose DMEM supplemented with 10% FBS from source A. Subsequent results demonstrated that co-culture of hBM-MSCs and MDA-MB-231 cells dramatically reduced invasiveness of both cell lines (F(1,4) = 71.465, p = 0.001) when embedded into a matrix comprising of growth-factor reduced base membrane extract (BME) and collagen.
机译:间充质干细胞已被广泛涉及肿瘤发育和转移。从使用二维(2D)模型转向三维(3D)来研究这种关系对于促进更适用和对肿瘤微环境的相关研究至关重要。我们研究了改变葡萄糖浓度和胎牛血清(FBS)的源于两种乳腺癌细胞系(T47D和MDA-231)和人骨髓衍生的间充质干细胞(HBM-MSC)的生长的影响确定成功的条件,以使其在3D肿瘤球体模型中的共同培养。随后,使用这些3D多细胞肿瘤球状球体来研究HBM-MSCs对乳腺癌细胞侵袭性的影响。本文提出的发现表明,血清源对在所有三种细胞系中测量的三分之二的生长参数的统计学显着影响,而葡萄糖仅对6%具有统计学显着的影响。确定用于3D HBM-MSCs和乳腺癌细胞系球体的共培养的最佳生长培养基组合物为1g / L葡萄糖DMEM,补充了来自源A的10%FBS。随后的结果表明HBM的共同培养当嵌入到包含生长因子降低的基膜提取物(BME)和胶原的基质中,MDS和MDA-MB-231细胞显着降低了细胞系(F(1,4)= 71.465,P = 0.001)的侵袭性。

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