Chen Hui William, Medley Colin D, Sefah Kwame, Shangguan Dihua, Tang Zhiwen, Meng Ling, Smith Josh E, Tan Weihong
Shands Cancer Center, Department of Chemistry, UF Genetics Institute and McKnight Brain Institute, University of Florida, Gainesville, FL 32611-7200, USA.
ChemMedChem. 2008 Jun;3(6):991-1001. doi: 10.1002/cmdc.200800030.
Early diagnosis is the way to improve the rate of lung cancer survival, but is almost impossible today due to the lack of molecular probes that recognize lung cancer cells sensitively and selectively. We developed a new aptamer approach for the recognition of specific small-cell lung cancer (SCLC) cell-surface molecular markers. Our approach relies on cell-based systematic evolution of ligands by exponential enrichment (cell-SELEX) to evolve aptamers for whole live cells that express a variety of surface markers representing molecular differences among cancer cells. When applied to different lung cancer cells including those from patient samples, these aptamers bind to SCLC cells with high affinity and specificity in various assay formats. When conjugated with magnetic and fluorescent nanoparticles, the aptamer nanoconjugates could effectively extract SCLC cells from mixed cell media for isolation, enrichment, and sensitive detection. These studies demonstrate the potential of the aptamer approach for early lung cancer detection.
早期诊断是提高肺癌生存率的途径,但由于缺乏能灵敏且选择性地识别肺癌细胞的分子探针,目前几乎无法实现。我们开发了一种新的适体方法来识别特定的小细胞肺癌(SCLC)细胞表面分子标记物。我们的方法依赖基于细胞的指数富集配体系统进化技术(细胞SELEX),来为表达各种代表癌细胞间分子差异的表面标记物的全活细胞进化适体。当应用于包括患者样本来源的不同肺癌细胞时,这些适体在各种检测形式中都能以高亲和力和特异性与SCLC细胞结合。当与磁性和荧光纳米颗粒偶联时,适体纳米缀合物能够从混合细胞培养基中有效提取SCLC细胞,用于分离、富集和灵敏检测。这些研究证明了适体方法在早期肺癌检测中的潜力。