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Tracking and Finding Slow-Proliferating/Quiescent Cancer Stem Cells with Fluorescent Nanodiamonds

机译:用荧光纳米金刚石跟踪和发现慢增殖/静止的癌症干细胞

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Quiescent cancer stem cells (CSCs) have long been considered to be a source of tumor initiation. However, identification and isolation of these cells have been hampered by the fact that commonly used fluorescent markers are not sufficiently stable, both chemically and photophysically, to allow tracking over an extended period of time. Here, it is shown that fluorescent nanodiamonds (FNDs) are well suited for this application. Genotoxicity tests of FNDs with comet and micronucleus assays for human fibroblasts and breast cancer cells indicate that the nanoparticles neither cause DNA damage nor impair cell growth. Using AS-B145-1R breast cancer cells as the model cell line for CSC, it is found that the FND labeling outperforms 5-ethynyl-2'-deoxyuridine (EdU) and carboxyfl uorescein diacetate succinimidyl ester (CFSE) in regards to its long-term tracking capability (> 20 d). Moreover, through a quantification of their stem cell activity by measuring mammosphere-forming efficiencies (MFEs) and self-renewal rates, the FND-positive cells are identified to have an MFE twice as high as that of the FND-negative cells isolated from the same dissociated mammospheres. Thus, the nanoparticle-based labeling technique provides an effective new tool for tracking and finding slow-proliferating/quiescent CSCs in cancer research.
机译:长期以来,人们一直认为静态癌症干细胞(CSC)是引发肿瘤的根源。但是,由于常用的荧光标记物在化学和光物理上都不够稳定,无法在较长时间内进行跟踪,因此妨碍了这些细胞的鉴定和分离。在此,表明荧光纳米金刚石(FND)非常适合此应用。 FNDs的彗星和微核试验对人类成纤维细胞和乳腺癌细胞的遗传毒性测试表明,纳米颗粒既不会引起DNA损伤,也不会损害细胞生长。使用AS-B145-1R乳腺癌细胞作为CSC的模型细胞系,发现FND标记在其长效方面优于5-乙炔基-2'-脱氧尿苷(EdU)和羧基荧光素二乙酸琥珀酰亚胺酯(CFSE)。长期跟踪能力(> 20天)。此外,通过测量哺乳动物小球形成效率(MFE)和自我更新率来量化其干细胞活性,鉴定出FND阳性细胞的MFE值是从分离的FND阴性细胞中获得的MFE值的两倍。相同的分离的乳球。因此,基于纳米颗粒的标记技术提供了一种有效的新工具,可用于追踪和发现癌症研究中缓慢增殖/静止的CSC。

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