Domura Ryota, Sasaki Rie, Okamoto Masami, Hirano Minoru, Kohda Katsunori, Napiwocki Brett, Turng Lih-Sheng
Advanced Polymeric Nanostructured Materials Engineering, Graduate School of Engineering, Toyota Technological Institute, 2-12-1 Hisakata, Tempaku, Nagoya 468 8511, Japan.
J Mater Chem B. 2017 Apr 14;5(14):2588-2600. doi: 10.1039/c7tb00207f. Epub 2017 Mar 15.
The progress of microenvironment-mediated tumor progression in an artificial extracellular matrix explores the design criteria to understand the cancer progression mechanism and metastatic potential. This study was aimed at examining the combination of both surface topographies (fiber alignments) and different stiffness of polymeric substrates (PLLA and PCL) to evaluate the effects on the cellular morphologies, proliferation, motility, and gene expression regarding epithelial to mesenchymal transition (EMT) of two different types of breast cancer cells (MDA-MB-231 and MCF-7). The cellular morphologies (roundness and nuclear elongation factor), E-cadherin and vimentin expression, and cellular motility in terms of cellular migration speed, persistent time, and diffusivity have been comprehensively discussed. We demonstrated that the microenvironment of cell culture substrates influences cancer progression and metastatic potential.
人工细胞外基质中介导的肿瘤进展研究探索了理解癌症进展机制和转移潜能的设计标准。本研究旨在考察两种表面形貌(纤维排列)与不同硬度的聚合物基质(聚左旋乳酸和聚己内酯)的组合,以评估其对两种不同类型乳腺癌细胞(MDA-MB-231和MCF-7)的细胞形态、增殖、迁移及上皮-间质转化(EMT)相关基因表达的影响。文中全面讨论了细胞形态(圆度和核伸长因子)、E-钙黏蛋白和波形蛋白的表达,以及细胞迁移速度、持续时间和扩散率方面的细胞迁移能力。我们证明了细胞培养基质的微环境会影响癌症进展和转移潜能。