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RNA quantification using gold nanoprobes - application to cancer diagnostics

机译:使用金纳米探针进行RNA定量-在癌症诊断中的应用

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摘要

Molecular nanodiagnostics applied to cancer may provide rapid and sensitive detection of cancer related molecular alterations, which would enable early detection even when those alterations occur only in a small percentage of cells. The use of gold nanoparticles derivatized with thiol modified oligonucleotides (Au-nanoprobes) for the detection of specific nucleic acid targets has been gaining momentum as an alternative to more traditional methodologies. Here, we present an Au-nanoparticles based approach for the molecular recognition and quantification of the BCR-ABL fusion transcript (mRNA), which is responsible for chronic myeloid leukemia (CML), and to the best of our knowledge it is the first time quantification of a specific mRNA directly in cancer cells is reported. This inexpensive and very easy to perform Au-nanoprobe based method allows quantification of unamplified total human RNA and specific detection of the oncogene transcript. The sensitivity settled by the Au-nanoprobes allows differential gene expression from 10 ng/μl of total RNA and takes less than 30 min to complete after total RNA extraction, minimizing RNA degradation. Also, at later stages, accumulation of malignant mutations may lead to resistance to chemotherapy and consequently poor outcome. Such a method, allowing for fast and direct detection and quantification of the chimeric BCR-ABL mRNA, could speed up diagnostics and, if appropriate, revision of therapy. This assay may constitute a promising tool in early diagnosis of CML and could easily be extended to further target genes with proven involvement in cancer development.
机译:应用于癌症的分子纳米诊断技术可以快速,灵敏地检测与癌症相关的分子变化,即使这些变化仅在很小比例的细胞中发生,也可以进行早期检测。作为更传统方法的替代方法,使用巯基修饰的寡核苷酸(Au-纳米探针)衍生的金纳米颗粒用于检测特定核酸靶标的势头越来越大。在这里,我们提出了一种基于金纳米颗粒的方法,用于分子识别和定量BCR-ABL融合转录本(mRNA),它负责慢性粒细胞白血病(CML),据我们所知,这是第一次报道了直接在癌细胞中定量特定mRNA的方法。这种廉价且非常容易执行的基于金纳米探针的方法可对未扩增的总人RNA进行定量,并对癌基因转录本进行特异性检测。金纳米探针解决的敏感性允许从10 ng /μl的总RNA中表达差异基因,并在提取总RNA后花费不到30分钟的时间完成,从而最大程度地减少了RNA降解。同样,在以后的阶段,恶性突变的积累可能导致对化学疗法的抵抗力,从而导致不良的预后。这种方法可以快速,直接地检测和定量嵌合BCR-ABL mRNA,可以加快诊断速度,并在适当的情况下加快治疗的速度。该测定法可能构成早期诊断CML的有前途的工具,可以很容易地扩展到进一步证明具有癌症发展作用的靶基因。

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