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利用多靶点浮力免疫微泡分离乳腺癌循环肿瘤细胞。

Isolation of Breast cancer CTCs with multitargeted buoyant immunomicrobubbles.

机构信息

Department of Pharmaceutical Sciences, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado Anschutz Medical Campus, 12850 East Montview Blvd., Aurora, CO 80045, USA.

Diagnologix, LLC, 5820 Oberlin Drive, Suite 104, San Diego, CA 92121, USA.

出版信息

Colloids Surf B Biointerfaces. 2018 Jan 1;161:200-209. doi: 10.1016/j.colsurfb.2017.10.060. Epub 2017 Oct 23.

DOI:10.1016/j.colsurfb.2017.10.060
PMID:29080504
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5726926/
Abstract

Circulating tumor cells (CTCs) are extremely rare cells found in blood of metastatic cancer patients. There is a need for inexpensive technologies for fast enrichment of CTCs from large blood volumes. Previous data showed that antibody-conjugated lipid shell immuno-microbubbles (MBs) bind and isolate cells from biological fluids by flotation. Here, blood-stable MBs targeted to several surface markers for isolation of breast tumor cells were developed. MBs coated with anti-human EpCAM antibodies showed efficient binding of EpCAM breast cancer cell lines SKBR-3, MCF-7, and MDA-MB-453, whereas anti-human EGFR MBs showed binding of EpCAM cell lines MDA-MB-231 and BT-549. Multitargeted anti-human EpCAM/EGFR MBs bound all cell lines with over 95% efficiency. Highly concentrated MB-bound tumor cells were collected in a microliter volume via an inverted vacuum-assisted harvesting setup. Using anti-EpCAM and/or anti-EpCAM/EGFR MBs, an efficient (70-90%) recovery and fast (30min) isolation of the above-mentioned cells and cell clusters was achieved from 7.5mL of spiked human blood. Using anti-EpCAM MBs and anti-EpCAM/EGFR MBs, cytokeratin-positive, CD45-negative CTCs were detected in 62.5% (10/16) of patients with metastatic breast cancer and CTC clusters were detected in 41.7% (5/12) of CTC-positive samples. Moreover, in some samples MBs isolated cytokeratin positive, CD45 negative tumor-derived microparticles. None of these structures were detected in blood from non-epithelial malignancies. The fast and inexpensive multitargeted platform for batch isolation of CTCs can promote research and clinical applications involving primary tumors and metastases.

摘要

循环肿瘤细胞(CTCs)是在转移性癌症患者血液中发现的极为罕见的细胞。需要开发廉价的技术,以便从大量血液中快速富集 CTCs。先前的数据表明,抗体偶联的脂质壳免疫微泡(MBs)通过浮选结合并从生物流体中分离细胞。这里,开发了针对几种表面标志物用于分离乳腺癌细胞的血液稳定的 MBs。用抗人 EpCAM 抗体包被的 MBs 显示出对 EpCAM 乳腺癌细胞系 SKBR-3、MCF-7 和 MDA-MB-453 的有效结合,而抗人 EGFR MBs 则显示出对 EpCAM 细胞系 MDA-MB-231 和 BT-549 的结合。多靶向抗人 EpCAM/EGFR MBs 以超过 95%的效率结合所有细胞系。通过倒置的真空辅助收获设置,以微升体积收集高度浓缩的 MB 结合的肿瘤细胞。使用抗 EpCAM 和/或抗 EpCAM/EGFR MBs,从 7.5mL 加标人血中实现了上述细胞和细胞簇的高效(70-90%)回收和快速(30min)分离。使用抗 EpCAM MBs 和抗 EpCAM/EGFR MBs,在 62.5%(10/16)的转移性乳腺癌患者中检测到细胞角蛋白阳性、CD45 阴性的 CTC,在 41.7%(5/12)的 CTC 阳性样本中检测到 CTC 簇。此外,在一些样本中,MBs 分离出细胞角蛋白阳性、CD45 阴性的肿瘤衍生的微颗粒。在非上皮性恶性肿瘤的血液中均未检测到这些结构。这种快速且廉价的多靶向 CTC 批量分离平台可以促进涉及原发性肿瘤和转移的研究和临床应用。

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UbcH10 a Major Actor in Cancerogenesis and a Potential Tool for Diagnosis and Therapy.UbcH10 是癌症发生的主要参与者,也是诊断和治疗的潜在工具。
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