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A Quantitative Perspective on Surface Marker Selection for the Isolation of Functional Tumor Cells

机译:定量标记的功能性肿瘤细胞分离的表面标志物选择。

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Much effort has gone into developing fluid biopsies of patient peripheral blood for the monitoring of metastatic cancers. One common approach is to isolate and analyze tumor cells in the peripheral blood. Widespread clinical implementation of this approach has been hindered by the current choice of targeting epithelial markers known to be highly variable in primary tumor sites. Here, we review current antigen-based tumor cell isolation strategies and offer biological context for commonly studied cancer surface markers. Expression levels of the most common markers are quantitated for three breast cancer and two non-small cell lung cancer (NSCLC) lineage models. These levels are contrasted with that present on healthy peripheral blood mononuclear cells (PBMC) for comparison to expected background levels in a fluid biopsy setting. A key feature of this work is establishing a metric of markers per square micrometer. This describes an average marker density on the cell membrane surface, which is a critical metric for emerging isolation strategies. These results serve to extend expression of key tumor markers in a sensitive and dynamic manner beyond traditional positiveegative immunohistochemical staining to guide future fluid biopsy targeting strategies.
机译:在开发用于监测转移性癌症的患者外周血的液体活检方面已经付出了很多努力。一种常见的方法是分离和分析外周血中的肿瘤细胞。当前选择靶向已知在原发肿瘤部位高度可变的上皮标记物已经阻碍了该方法的广泛临床实施。在这里,我们审查当前基于抗原的肿瘤细胞分离策略,并为经常研究的癌症表面标志物提供生物学背景。对三种乳腺癌和两种非小细胞肺癌(NSCLC)谱系模型量化最常见标志物的表达水平。这些水平与健康的外周血单个核细胞(PBMC)上存在的水平形成对比,以便与液体活检中的预期背景水平进行比较。这项工作的关键特征是建立每平方微米的标记度量。这描述了细胞膜表面上的平均标记物密度,这是新兴分离策略的关键指标。这些结果有助于以敏感和动态的方式扩展关键肿瘤标志物的表达,以超越传统的阳性/阴性免疫组织化学染色,以指导未来的液体活检靶向策略。

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