Cirello Valentina, Vaira Valentina, Grassi Elisa Stellaria, Vezzoli Valeria, Ricca Dario, Colombo Carla, Bosari Silvano, Vicentini Leonardo, Persani Luca, Ferrero Stefano, Fugazzola Laura
Endocrine Unit, Fondazione IRCCS Ca' Granda, 20122 Milan, Italy.
Department of Pathophysiology and Transplantation, University of Milan, 20122 Milan, Italy.
Oncotarget. 2017 Feb 7;8(6):9752-9766. doi: 10.18632/oncotarget.14187.
Multicellular three-dimensional (3D) spheroids represent an experimental model that is intermediate in its complexity between monolayer cultures and patients' tumor. In the present study, we characterize multicellular spheroids from papillary (PTC) and follicular (FTC) thyroid cancers and from the corresponding normal tissues. We show that these 3D structures well recapitulate the features of the original tissues, in either the differentiated and "stem-like" components. As a second step, we were aimed to test the effects of a small multikinase inhibitor, SP600125 (SP), previously shown to efficiently induce cell death in undifferentiated thyroid cancer monolayer cultures. We demonstrate the potent effect of SP on cell growth and survival in our 3D multicellular cultures. SP exerts its main effects through direct and highly significant inhibition of the ROCK pathway, known to be involved in the regulation of cell migration and β-catenin turnover. Consistently, SP treatment resulted in a significant decrease in β-catenin levels with respect to basal conditions in tumor but not in normal spheroids, indicating that the effect is promisingly selective on tumor cells.In conclusion, we provide the morphological and molecular characterization of thyroid normal and tumor spheroids. In this 3D model we tested in vitro the effects of the multikinase inhibitor SP and further characterized its mechanism of action in both normal and tumor spheroids, thus making it an ideal candidate for developing new drugs against thyroid cancer.
多细胞三维(3D)球体代表了一种实验模型,其复杂性介于单层培养物和患者肿瘤之间。在本研究中,我们对来自乳头状(PTC)和滤泡状(FTC)甲状腺癌以及相应正常组织的多细胞球体进行了表征。我们表明,这些3D结构很好地概括了原始组织在分化和“干细胞样”成分方面的特征。第二步,我们旨在测试一种小型多激酶抑制剂SP600125(SP)的作用,该抑制剂先前已证明能有效诱导未分化甲状腺癌单层培养物中的细胞死亡。我们证明了SP对我们的3D多细胞培养物中细胞生长和存活的强大作用。SP通过直接且高度显著地抑制ROCK途径发挥其主要作用,已知该途径参与细胞迁移和β-连环蛋白周转的调节。一致地,与肿瘤球体的基础条件相比,SP处理导致β-连环蛋白水平显著降低,但在正常球体中未出现这种情况,这表明该作用对肿瘤细胞具有有前景的选择性。总之,我们提供了甲状腺正常和肿瘤球体的形态学和分子表征。在这个3D模型中,我们在体外测试了多激酶抑制剂SP的作用,并进一步表征了其在正常和肿瘤球体中的作用机制,从而使其成为开发抗甲状腺癌新药的理想候选者。