Costa Elisabete C, Gaspar Vítor M, Coutinho Paula, Correia Ilídio J
CICS-UBI-Health Sciences Research Centre, Universidade da Beira Interior, 6200-506, Covilhã, Portugal.
Biotechnol Bioeng. 2014 Aug;111(8):1672-85. doi: 10.1002/bit.25210. Epub 2014 Feb 25.
Three-dimensional (3D) cell culture models of solid tumors are currently having a tremendous impact in the in vitro screening of candidate anti-tumoral therapies. These 3D models provide more reliable results than those provided by standard 2D in vitro cell cultures. However, 3D manufacturing techniques need to be further optimized in order to increase the robustness of these models and provide data that can be properly correlated with the in vivo situation. Therefore, in the present study the parameters used for producing multicellular tumor spheroids (MCTS) by liquid overlay technique (LOT) were optimized in order to produce heterogeneous cellular agglomerates comprised of cancer cells and stromal cells, during long periods. Spheroids were produced under highly controlled conditions, namely: (i) agarose coatings; (ii) horizontal stirring, and (iii) a known initial cell number. The simultaneous optimization of these parameters promoted the assembly of 3D characteristic cellular organization similar to that found in the in vivo solid tumors. Such improvements in the LOT technique promoted the assembly of highly reproducible, individual 3D spheroids, with a low cost of production and that can be used for future in vitro drug screening assays.
实体瘤的三维(3D)细胞培养模型目前在候选抗肿瘤疗法的体外筛选中产生了巨大影响。这些3D模型比标准的二维体外细胞培养模型提供更可靠的结果。然而,3D制造技术需要进一步优化,以提高这些模型的稳健性,并提供能够与体内情况进行适当关联的数据。因此,在本研究中,对通过液体覆盖技术(LOT)生产多细胞肿瘤球体(MCTS)所使用的参数进行了优化,以便长时间产生由癌细胞和基质细胞组成的异质细胞聚集体。球体在高度受控的条件下产生,即:(i)琼脂糖涂层;(ii)水平搅拌,以及(iii)已知的初始细胞数量。这些参数的同时优化促进了类似于体内实体瘤中发现的三维特征性细胞组织的组装。LOT技术的这种改进促进了高度可重复的单个3D球体的组装,生产成本低,可用于未来的体外药物筛选试验。