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A novel method for downstream characterization of breast cancer circulating tumor cells following CellSearch isolation

机译:CellSearch分离后用于乳腺癌循环肿瘤细胞下游表征的新方法

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Background Enumeration of circulating tumor cells (CTCs) obtained from minimally invasive blood samples has been well established as a valuable monitoring tool in metastatic and early breast cancer, as well as in several other cancer types. The gold standard technology for detecting CTCs in blood against a backdrop of millions of leukocytes is the FDA-approved CellSearch system (Janssen Diagnostics), which relies on EpCAM-based immunomagnetic separation. Secondary characterization of these cells could enable treatment selection based on specific targets in these cells, as well as providing a real time window into the metastatic process and offering unique insights into tumor heterogeneity. The objective of this study was to develop a method for downstream characterization of CTCs following isolation with the CellSearch system. Methods An in vitro CTC model system focusing on clinically useful treatment predictive biomarkers in breast cancer, specifically the estrogen receptor α (ERα) and the human epidermal growth factor receptor 2 (HER2), was established using healthy donor blood spiked with breast cancer cell lines MCF7 (ERα+/HER2?) and SKBr3 (ERα?/HER2+). Following CTC isolation by CellSearch, the captured CTCs were further enriched and fixed on a microscope slide using the in-house-developed CTC-DropMount technique. Results The recovery rate of CTCs after CellSearch Profile analysis and CTC-DropMount was 87%. A selective and consistent triple-immunostaining protocol was optimized. Cells positive for DAPI, cytokeratin (CK) 8, 18 and 19, but negative for the leukocyte-specific marker CD45, were classified as CTCs and subsequently analyzed for ERα and HER2 expression. The method was verified in breast cancer patient samples, thus demonstrating its clinical relevance. Conclusions Our results show that it is possible to ascertain the status of important predictive biomarkers expressed in breast cancer CTCs using the newly developed CTC-DropMount technique. Downstream characterization of multiple biomarkers using a standard fluorescence microscope demonstrates that important clinical and biological information may be obtained from a single patient blood sample following either CellSearch epithelial or profile analyses. Trial registration Clinical Trials NCT01322893
机译:背景技术从微创血液样本中获取的循环肿瘤细胞(CTC)枚举已被广泛确立为转移性和早期乳腺癌以及其他几种癌症类型的重要监测工具。 FDA批准的CellSearch系统(Janssen Diagnostics)是在数百万白细胞背景下检测血液中CTC的金标准技术,该系统依赖于基于EpCAM的免疫磁分离。这些细胞的二级表征可以基于这些细胞中的特定靶标进行治疗选择,并提供进入转移过程的实时窗口并提供对肿瘤异质性的独特见解。这项研究的目的是开发一种用CellSearch系统隔离后对CTC进行下游表征的方法。方法使用掺有乳腺癌细胞系的健康供体血液,建立以乳腺癌临床上有用的治疗预测性生物标志物为重点的体外CTC模型系统,特别是雌激素受体α(ERα)和人表皮生长因子受体2(HER2)。 MCF7(ERα + / HER2 ?)和SKBr3(ERα? / HER2 + )。通过CellSearch隔离CTC之后,使用内部开发的CTC-DropMount技术将捕获的CTC进一步富集并固定在显微镜载玻片上。结果CellSearch Profile分析和CTC-DropMount分析后的CTC回收率为87%。优化了选择性一致的三重免疫染色方案。 DAPI阳性的细胞角蛋白(CK)8、18和19,但白细胞特异性标记CD45阴性的细胞被分类为CTC,随后分析ERα和HER2的表达。该方法已在乳腺癌患者样本中得到验证,从而证明了其临床相关性。结论我们的结果表明,使用最新开发的CTC-DropMount技术可以确定在乳腺癌CTC中表达的重要预测性生物标志物的状态。使用标准荧光显微镜对多种生物标志物进行下游表征表明,在CellSearch上皮或谱图分析之后,可以从单个患者的血液样本中获得重要的临床和生物学信息。试验注册临床试验NCT01322893

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