利用成像质谱仪对液体活检中的循环肿瘤细胞进行多重蛋白质检测。

Convergent science physical oncology Pub Date : 2018-03-01 Epub Date: 2018-01-16 DOI:10.1088/2057-1739/aaa013
Erik Gerdtsson, Milind Pore, Jana-Aletta Thiele, Anna Sandström Gerdtsson, Paymaneh D Malihi, Rafael Nevarez, Anand Kolatkar, Carmen Ruiz Velasco, Sophia Wix, Mohan Singh, Anders Carlsson, Amado J Zurita, Christopher Logothetis, Akil A Merchant, James Hicks, Peter Kuhn
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引用次数: 0

摘要

循环和播散肿瘤细胞(CTCs/DTCs)的分子分析作为一种通过微创液体活检近实时连续评估预后和治疗效果的手段,具有巨大的潜力。然而,要实现这一潜力,必须开发并验证对这些罕见细胞进行分子分析的方法。在这里,我们介绍了使用金属标记抗体的成像质控细胞仪(IMC)在 Fluidigm Hyperion 成像系统上的应用,以及图像分析和信号归一化的方法。通过使用转移性前列腺癌病例的液体活检,我们证明了 IMC 能将 CTC 特征描述的范围扩大到数十种蛋白质生物标记物,并能同时对数千个白细胞进行表型,从而了解可能影响治疗反应、转移和免疫监视的一系列生物特性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Multiplex protein detection on circulating tumor cells from liquid biopsies using imaging mass cytometry.

Multiplex protein detection on circulating tumor cells from liquid biopsies using imaging mass cytometry.

Multiplex protein detection on circulating tumor cells from liquid biopsies using imaging mass cytometry.

Multiplex protein detection on circulating tumor cells from liquid biopsies using imaging mass cytometry.

Molecular analysis of circulating and disseminated tumor cells (CTCs/DTCs) has great potential as a means for continuous evaluation of prognosis and treatment efficacy in near-real time through minimally invasive liquid biopsies. To realize this potential, however, methods for molecular analysis of these rare cells must be developed and validated. Here, we describe the integration of imaging mass cytometry (IMC) using metal-labeled antibodies as implemented on the Fluidigm Hyperion Imaging System into the workflow of the previously established High Definition Single Cell Analysis (HD-SCA) assay for liquid biopsies, along with methods for image analysis and signal normalization. Using liquid biopsies from a metastatic prostate cancer case, we demonstrate that IMC can extend the reach of CTC characterization to include dozens of protein biomarkers, with the potential to understand a range of biological properties that could affect therapeutic response, metastasis and immune surveillance when coupled with simultaneous phenotyping of thousands of leukocytes.

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