Domura Ryota, Sasaki Rie, Ishikawa Yuma, Okamoto Masami
Advanced Polymeric Nanostructured Materials Engineering, Graduate School of Engineering, Toyota Technological Institute, 2-12-1 Hisakata, Tempaku, Nagoya 468 8511, Japan.
J Funct Biomater. 2017 Jun 6;8(2):18. doi: 10.3390/jfb8020018.
The interpretation of the local microenvironment of the extracellular matrix for malignant tumor cells is in intimate relation with metastatic spread of cancer cells involving the associated issues of cellular proliferation and drug responsiveness. This study was aimed to assess the combination of both surface topographies (fiber alignments) and different stiffness of the polymeric substrates (poly(l-lactic acid) and poly(ε-caprolactone), PLLA and PCL, respectively) as well as collagen substrates (coat and gel) to elucidate the effect of the cellular morphology on cellular proliferation and drug sensitivities of two different types of breast cancer cells (MDA-MB-231 and MCF-7). The morphological spreading parameter (nucleus/cytoplasm area ratio) induced by the anthropogenic substrates has correlated intimately with the cellular proliferation and the drug sensitivity the half maximal inhibitory concentration (IC) of cancer cells. This study demonstrated the promising results of the parameter for the evaluation of cancer cell malignancy.
细胞外基质对恶性肿瘤细胞的局部微环境的解读与癌细胞的转移扩散密切相关,其中涉及细胞增殖和药物反应性等相关问题。本研究旨在评估两种表面形貌(纤维排列)以及不同硬度的聚合物基质(分别为聚(L-乳酸)和聚(ε-己内酯),即聚乳酸(PLLA)和聚己内酯(PCL)),以及胶原基质(涂层和凝胶)的组合,以阐明细胞形态对两种不同类型乳腺癌细胞(MDA-MB-231和MCF-7)的细胞增殖和药物敏感性的影响。人为基质诱导的形态扩展参数(核/质面积比)与细胞增殖以及癌细胞的半数最大抑制浓度(IC)药物敏感性密切相关。本研究证明了该参数在评估癌细胞恶性程度方面的良好结果。