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组蛋白去乙酰化酶抑制剂引起的生物阻抗增加是混合培养正常乳腺细胞中乳腺癌细胞的标志物。

Bioimpedance rise in response to histone deacetylase inhibitor is a marker of mammary cancer cells within a mixed culture of normal breast cells.

机构信息

VT MEMS Lab, The Bradley Department of Electrical and Computer Engineering, Virginia Tech. Blacksburg, Virginia 24061, United States.

出版信息

Lab Chip. 2012 Dec 21;12(24):5168-79. doi: 10.1039/c2lc40778g.

DOI:10.1039/c2lc40778g
PMID:23108380
Abstract

Detection of a few cancer cells within a complex cellular mixture is a key challenge presented by clinical human biopsy samples. We have designed and tested a microfabricated bioimpedance device that can detect a few human MDA-MB-231 breast cancer cells in a mixed cell culture model of a breast tissue sample. The normal tissue components were modelled using non-cancerous MCF10A human breast epithelial cells and normal human HS68 fibroblasts. The sensor is a silicon chip 0.5 cm in diameter that contains one counter electrode and four 40 μm-wide multi-branched sensing electrodes. The cells' bioimpedances were characterized in pure monocultures and in mixed cell cultures following a brief cultivation on the sensor. After cell seeding, a stable bioimpedance signal was achieved indicative of cell attachment. A cancer-selective bioimpedance signal was elicited by addition of suberoylanilide hydroxamic acid (SAHA), a histone deacetylase inhibitor with selective actions on the cytoskeleton in breast cancer cells. SAHA elicited a 50% rise in peak bioimpedance in MDA-MB-231 breast cancer cells by 15 h. In mixed cultures of MDA-MB-231, MCF10A, and HS68 cells, the contribution of cancer cells present in the mixture dominated impedance response to SAHA. A single adherent cancer cell on any one of four electrodes in a background of ∼100 normal cells resulted in ≥5% increase in bioimpedance. The estimated sensitivity of this device is therefore one cancer cell among a background of 400 normal cells or the equivalent of 25 cancer cells in a biopsy sample of 10 000 cells.

摘要

在复杂的细胞混合物中检测少量癌细胞是临床人体活检样本提出的一个关键挑战。我们设计并测试了一种微制造的生物阻抗设备,可以在乳腺组织样本的混合细胞培养模型中检测少量人 MDA-MB-231 乳腺癌细胞。正常组织成分使用非癌性 MCF10A 人乳腺上皮细胞和正常的人 HS68 成纤维细胞建模。传感器是一个直径为 0.5 厘米的硅芯片,包含一个对电极和四个 40μm 宽的多分支传感电极。在传感器上短暂培养后,对纯单培养物和混合细胞培养物中的细胞生物阻抗进行了表征。细胞接种后,获得了稳定的生物阻抗信号,表明细胞附着。通过添加琥珀酰亚胺基羟肟酸(SAHA),一种在乳腺癌细胞中对细胞骨架具有选择性作用的组蛋白去乙酰化酶抑制剂,引发了癌症选择性的生物阻抗信号。在 15 小时内,SAHA 使 MDA-MB-231 乳腺癌细胞的峰值生物阻抗增加了 50%。在 MDA-MB-231、MCF10A 和 HS68 细胞的混合培养物中,混合物中存在的癌细胞对阻抗响应的贡献占主导地位。在背景中有 100 个正常细胞的情况下,在四个电极中的任何一个上单个贴壁癌细胞导致生物阻抗增加≥5%。因此,该设备的估计灵敏度为在 400 个正常细胞的背景中存在一个癌细胞,或在 10000 个细胞的活检样本中存在 25 个癌细胞。

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