Department of Chemistry, Kalamazoo College, 1200 Academy St., Kalamazoo, MI 49006, USA.
Anal Bioanal Chem. 2012 Aug;404(2):399-406. doi: 10.1007/s00216-012-6162-9. Epub 2012 Jun 13.
Mortality due to breast cancer is increasingly linked to early, undetected metastasis, making methods for earlier detection acutely necessary. We describe the development of an assay based on molecular beacon (MB) chemistry with fluorescence detection to monitor a breast cancer biomarker for the analysis of breast cancer metastasis. The MB assay is based on the complementary base-pairing interactions of the MB nucleic acid with mRNA indicative of breast cancer metastasis. The presence of mRNA is characterized by an increase in the fluorescence intensity of the molecular beacon. The assay gives a linear, reproducible response to prolactin inducible protein mRNA, with a limit of detection in the high picomolar range. This method sensitively and specifically identifies a biomarker directly in serum samples in minimal time and with a straightforward procedure, dramatically reducing the total time for sample analysis over current methods from days to hours. The potential impact of this work in detection and understanding of breast cancer metastasis lies in improvements in simplicity, accuracy, and speed over current methods, which could allow for improved patient treatment and prognoses. Ultimately, additional sample throughput will result in better understanding of disease progression.
乳腺癌导致的死亡率与早期未被发现的转移密切相关,这使得更早检测的方法变得非常必要。我们描述了一种基于分子信标 (MB) 化学和荧光检测的分析方法的开发,用于监测乳腺癌转移的乳腺癌生物标志物。MB 分析方法基于 MB 核酸与指示乳腺癌转移的 mRNA 的互补碱基配对相互作用。mRNA 的存在通过分子信标的荧光强度增加来表征。该分析方法对催乳素诱导蛋白 mRNA 呈现出线性、可重现的响应,检测限在高皮摩尔范围内。这种方法能够在最小的时间内以简单直接的程序,在血清样本中灵敏而特异性地识别生物标志物,与当前方法相比,大大减少了样品分析的总时间,从数天减少到数小时。这项工作在检测和理解乳腺癌转移方面的潜在影响在于,与当前方法相比,它在简单性、准确性和速度方面有所改进,这可能会改善患者的治疗和预后。最终,增加样本通量将有助于更好地了解疾病的进展。