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硅微结构中人乳腺癌细胞形态结构中抗癌药物琥珀酰亚胺基异羟肟酸(SAHA)的作用。

Actions of the anti-cancer drug suberoylanilide hydroxamic acid (SAHA) on human breast cancer cytoarchitecture in silicon microstructures.

机构信息

Department of Biomedical Sciences & Pathobiology, Virginia Tech, Blacksburg, VA 24061, USA.

出版信息

Biomaterials. 2010 Sep;31(27):7043-50. doi: 10.1016/j.biomaterials.2010.05.023. Epub 2010 Jun 25.

Abstract

Micro- and nanotechnologies are increasingly being applied in cancer research. Here we report the effects of an experimental breast cancer agent, SAHA, on the cytoarchitecture and adherence of MDA-MB-231 metastatic human breast cancer cells on flat silicon surfaces and in three dimensional (3-D) isotropic silicon microstructures. The 3-D silicon microstructure were fabricated using a single mask and single etch step process to yield arrays of star- and circular-shaped microchambers 151-168 microm in diameter and 53-68 microm deep. There was a marked expansion of the microtubule network, an increase in mean cell area and mean cell length in response to SAHA. SAHA also decreased the nuclear-to-cytoplasmic area (N/C). Atomic force microscopy (AFM) showed there was no change in cellular elasticity over the nuclear region in response to SAHA. The alterations in cytoarchitecture produced by SAHA were associated with changes in the mode of adhesion of the cells in silicon microstructures. In contrast to control cells which conformed to the microstructures, SAHA caused cells to stretch and attach to the microstructures through actin-rich cell extensions. We conclude that isotropically etched silicon microstructures comprise microenvironments that discriminate metastatic mammary cancer cells in which cytoskeletal elements reorganized in response to the anti-cancer agent SAHA.

摘要

微纳技术在癌症研究中的应用日益广泛。在这里,我们报告了一种实验性乳腺癌药物 SAHA 对 MDA-MB-231 转移性人乳腺癌细胞在平面硅表面和三维(3-D)各向同性硅微结构中的细胞结构和黏附的影响。3-D 硅微结构采用单一掩模和单一刻蚀工艺制造,得到直径为 151-168 微米、深度为 53-68 微米的星形和圆形微腔阵列。微管网络明显扩张,细胞面积和长度的平均值增加,对 SAHA 有反应。SAHA 还降低了核质比(N/C)。原子力显微镜(AFM)显示,SAHA 作用于核区时,细胞弹性没有变化。SAHA 引起的细胞结构变化与细胞在硅微结构中的黏附方式的变化有关。与符合微结构的对照细胞不同,SAHA 导致细胞通过富含肌动蛋白的细胞延伸伸展并附着到微结构上。我们得出结论,各向同性刻蚀硅微结构构成了微环境,可区分对癌细胞有反应的转移性乳腺癌细胞,其中细胞骨架元件在抗癌药物 SAHA 的作用下重新组织。

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