首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Isolating Highly Enriched Populations Of Circulating Epithelial Cells And Other Rare Cells From Blood Using A Magnetic Sweeper Device
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Isolating Highly Enriched Populations Of Circulating Epithelial Cells And Other Rare Cells From Blood Using A Magnetic Sweeper Device

机译:使用磁扫装置从血液中分离出高度富集的循环上皮细胞和其他稀有细胞

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The enumeration of rare circulating epithelial cells (CEpCs) in the peripheral blood of metastatic cancer patients has shown promise for improved cancer prognosis. Moving beyond enumeration, molecular analysis of CEpCs may provide candidate surrogate endpoints to diagnose, treat, and monitor malignancy directly from the blood samples. Thorough molecular analysis of CEpCs requires the development of new sample preparation methods that yield easily accessible and purified CEpCs for downstream biochemical assays. Here, we describe a new immunomagnetic cell separator, the MagSweeper, which gently enriches target cells and eliminates cells that are not bound to magnetic particles. The isolated cells are easily accessible and can be extracted individually based on their physical characteristics to deplete any cells nonspe-cifically bound to beads. We have shown that our device can process 9 mL of blood per hour and captures >50% of CEpCs as measured in spiking experiments. We have shown that the separation process does not perturb the gene expression of rare cells. To determine the efficiency of our platform in isolating CEpCs from patients, we have isolated CEpCs from all 47 tubes of 9-mL blood samples collected from 17 women with metastatic breast cancer. In contrast, we could not find any circulating epithelial cells in samples from 5 healthy donors. The isolated CEpCs are all stored individually for further molecular analysis.
机译:转移性癌症患者外周血中稀有循环上皮细胞(CEpC)的计数显示了改善癌症预后的希望。超越枚举,CEpCs的分子分析可以提供候选替代终点,直接从血样中诊断,治疗和监测恶性肿瘤。对CEpC进行彻底的分子分析要求开发新的样品制备方法,以产生易于获得和纯化的CEpC,用于下游生化分析。在这里,我们描述了一种新型的免疫磁性细胞分离器MagSweeper,它可以缓慢富集靶细胞并消除未与磁性颗粒结合的细胞。分离的细胞很容易接近,可以根据它们的物理特性进行单独提取,以耗尽非特异性结合于珠子的任何细胞。我们已经证明,我们的设备每小时可处理9 mL血液,并在加标实验中捕获到超过50%的CEpC。我们已经表明,分离过程不会干扰稀有细胞的基因表达。为了确定我们平台从患者中分离CEpC的效率,我们从所有47支9毫升血液样本试管中分离出了CEpC,这些样本均采集自17例转移性乳腺癌妇女。相比之下,我们在来自5位健康供体的样本中找不到任何循环上皮细胞。分离的CEpC均单独存储以进行进一步的分子分析。

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