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一种用于研究神经元与癌细胞相互作用的芯片模型。

An on-chip model for investigating the interaction between neurons and cancer cells.

作者信息

Lei Yifeng, Li Jun, Wang Nuoxin, Yang Xinglong, Hamada Yoh, Li Qizhai, Zheng Wenfu, Jiang Xingyu

机构信息

Beijing Engineering Research Center for BioNanotechnology, CAS Key Laboratory for Biological Effects of Nanomaterials and Nanosafety, National Center for NanoScience and Technology, Beijing 100190, China.

Department of Nano-Medical Science, Graduate School of Medicine, Tohoku University, Sendai 980-8575, Japan.

出版信息

Integr Biol (Camb). 2016 Mar 14;8(3):359-67. doi: 10.1039/c5ib00309a.

Abstract

Emerging evidence suggests that there is extensive interaction between neurons and cancer cells. However, few model systems have been developed to investigate nerve-cancer cell interaction in vitro. Herein, a high-throughput microfluidic compartmentalized chip is developed to examine the interaction between neurons and cancer cells. The nerve bundles appear to provide a biophysical support for cancer cells and guide their directional migration. The cancers that have high levels of perineural invasion in clinical observations exhibit greater migration along neurites in the on-chip model. The on-chip model allows the screening of compounds which inhibit cancer cell migration along neurites in vitro. The interruption of neurites, the pharmacological blockade of nerve-cancer signaling, effectively attenuates the migration of cancer cells along neurites. This on-chip model provides a useful platform to investigate the dynamic interaction between cancer cells and neurons and can dramatically broaden the chemical space in screening neuron-related drugs for cancers.

摘要

新出现的证据表明,神经元与癌细胞之间存在广泛的相互作用。然而,很少有模型系统被开发用于在体外研究神经-癌细胞的相互作用。在此,开发了一种高通量微流控分隔芯片来检测神经元与癌细胞之间的相互作用。神经束似乎为癌细胞提供了生物物理支持并引导其定向迁移。在临床观察中具有高水平神经周围浸润的癌症在芯片模型中沿神经突表现出更大的迁移。该芯片模型允许筛选在体外抑制癌细胞沿神经突迁移的化合物。神经突的中断,即神经-癌症信号的药理学阻断,有效地减弱了癌细胞沿神经突的迁移。这种芯片模型为研究癌细胞与神经元之间的动态相互作用提供了一个有用的平台,并且可以极大地拓宽筛选用于癌症的神经元相关药物的化学空间。

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