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在成纤维细胞饲养层上利用基于磁力的共培养法进行循环肿瘤细胞的体外培养。

Ex vivo culture of circulating tumor cells using magnetic force-based coculture on a fibroblast feeder layer.

作者信息

Yamamoto Shuhei, Shimizu Kazunori, Fei Jiahui, Iwata Hiroji, Okochi Mina, Nakanishi Hayao, Honda Hiroyuki

机构信息

Department of Biotechnology, Graduate School of Engineering, Nagoya University, Nagoya, Japan.

Department of Breast Oncology, Aichi Cancer Center Central Hospital, Nagoya, Japan.

出版信息

Biotechnol J. 2016 Nov;11(11):1433-1442. doi: 10.1002/biot.201600084. Epub 2016 Oct 31.

Abstract

Phenotype-based analysis of circulating tumor cells (CTCs) is a promising approach to identification of new therapeutic targets and to elucidation of the biological properties. Nonetheless, ex vivo culturing of CTCs is still a technical challenge. Here, we develop a novel ex vivo culture method for CTCs using a fibroblast feeder layer and a magnetic coculture protocol. CTCs in the blood of a mouse metastasis model are labeled magnetically with magnetite nanoparticles. The labeled CTCs are isolated by a magnetic capture column and a size-selective capture filter. The isolated CTCs are positioned on a fibroblast feeder layer by the magnetic force. As a result, we observe adhesion and proliferation of the CTCs under the conditions of the fibroblast feeder layer and the magnetic force, whereas no adhesion or proliferation is observed without the feeder layer. After that, we culture the CTCs and obtain three CTC-derived cell lines. Using these cell lines, we perform phenotype-based analyses of invasiveness and drug resistance and find that the CTC-derived cell lines are more malignant than the original cells. Thus, the proposed method would be a promising approach to ex vivo culture of CTCs for phenotype-based analysis, and possibly used in cancer treatment.

摘要

基于表型的循环肿瘤细胞(CTC)分析是识别新治疗靶点和阐明生物学特性的一种有前景的方法。尽管如此,CTC的体外培养仍然是一项技术挑战。在此,我们开发了一种使用成纤维细胞饲养层和磁性共培养方案的新型CTC体外培养方法。在小鼠转移模型的血液中的CTC用磁铁矿纳米颗粒进行磁性标记。通过磁性捕获柱和尺寸选择性捕获过滤器分离标记的CTC。通过磁力将分离的CTC置于成纤维细胞饲养层上。结果,我们观察到在成纤维细胞饲养层和磁力条件下CTC的黏附和增殖,而在没有饲养层的情况下未观察到黏附或增殖。之后,我们培养CTC并获得三个源自CTC的细胞系。使用这些细胞系,我们进行基于表型的侵袭性和耐药性分析,发现源自CTC的细胞系比原始细胞更具恶性。因此,所提出的方法将是一种用于基于表型分析的CTC体外培养的有前景的方法,并可能用于癌症治疗。

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