Park Min Hee, Song Boa, Hong Seungpyo, Kim Sang Heon, Lee Kangwon
Center for Biomaterials, Korea Institute of Science and Technology , Seoul 02792, Republic of Korea.
Department of Biomedical Engineering, University of Science and Technology , Daejeon 34113, Republic of Korea.
Mol Pharm. 2016 Jul 5;13(7):2204-13. doi: 10.1021/acs.molpharmaceut.5b00953. Epub 2016 May 19.
Invasion and metastasis of cancer directly related to human death have been associated with interactions among many different types of cells and three-dimensional (3D) tissue matrices. Precise mechanisms related to cancer invasion and metastasis still remain unknown due to their complexities. Development of tumor microenvironment (TME)-mimicking system could play a key role in understanding cancer environments and in elucidating the relating phenomena and their driving forces. Here we report a facile and novel platform of 3D cancer cell-clusters using human adipose-derived mesenchymal stem cells (hASCs) and breast cancer cells (MDA-MB-231) within a collagen gel matrix to show cancer invasion in the cell and extracellular matrix (ECM). Both clusters A (hASC only) and AC (hASC and MDA-MB-231) exhibited different behaviors and expressions of migration and invasion, as observed by the relating markers such as fibronectin, α-SMA, and CXCR4. hASCs showed a protrusive migration from a cluster center, whereas MDA-MB-231 spread out radially followed by hASC migration. Finally, the effect of matrix was further discussed by varying collagen gel densities. The new biomimetic system of 3D cancer clusters developed here has the potential to be utilized for research on migration and invasion of cancer cells in extracellular matrices.
癌症的侵袭和转移直接关乎人类死亡,这与多种不同类型细胞和三维(3D)组织基质之间的相互作用有关。由于其复杂性,与癌症侵袭和转移相关的精确机制仍然未知。构建模拟肿瘤微环境(TME)的系统可能在理解癌症环境以及阐明相关现象及其驱动因素方面发挥关键作用。在此,我们报告了一种简便且新颖的3D癌细胞团簇平台,该平台利用人脂肪来源的间充质干细胞(hASC)和乳腺癌细胞(MDA-MB-231)在胶原蛋白凝胶基质中展示细胞和细胞外基质(ECM)中的癌症侵袭。通过诸如纤连蛋白、α-SMA和CXCR4等相关标志物观察到,A簇(仅hASC)和AC簇(hASC和MDA-MB-231)在迁移和侵袭方面表现出不同的行为和表达。hASC从团簇中心呈突出状迁移,而MDA-MB-231呈放射状扩散,随后hASC迁移。最后,通过改变胶原蛋白凝胶密度进一步探讨了基质的作用。此处开发的新型3D癌症团簇仿生系统有潜力用于研究癌细胞在细胞外基质中的迁移和侵袭。