Centre National de la Recherche Scientifique, LBCMCP UMR5088, Toulouse, France.
Cancer Biol Ther. 2009 Dec;8(23):2230-36. doi: 10.4161/cbt.8.23.9984. Epub 2009 Dec 3.
Multicellular tumor spheroids closely mimic the 3D organization of avascular microregions within tumors and thereby represent a valuable model for the evaluation of anticancer drugs. In this study, we performed a 3D analysis of the response to the CDC25 phosphatase inhibitor IRC-083864 in HCT116 spheroids. Continuous exposure to IRC-083864 strongly inhibits the growth of spheroids and is shown to correlate with a decrease in Ki-67 positive cells. The cytotoxicity induced by IRC-083864 was examined by two-photon laser microscopy imaging and 3D reconstruction. Visualization in 3D allowed us to demonstrate that IRC-083864 treatment results in the inhibition of mitosis and induces cell death specifically localized in the outer proliferative cell layers of the spheroid structure. These results emphasize the importance of 3D models and of in toto analysis for the evaluation of anticancer drugs cytotoxicity.
多细胞肿瘤球体紧密模拟了肿瘤内无血管微区域的 3D 组织,因此代表了评估抗癌药物的有价值的模型。在这项研究中,我们对 HCT116 球体中对 CDC25 磷酸酶抑制剂 IRC-083864 的反应进行了 3D 分析。持续暴露于 IRC-083864 强烈抑制球体的生长,并显示与 Ki-67 阳性细胞的减少相关。通过双光子激光显微镜成像和 3D 重建来检查 IRC-083864 诱导的细胞毒性。在 3D 中的可视化使我们能够证明 IRC-083864 处理导致有丝分裂的抑制,并诱导细胞死亡,其特别定位于球体结构的外层增殖细胞层中。这些结果强调了 3D 模型和整体分析在评估抗癌药物细胞毒性方面的重要性。