Detection of YAP1 and AR-V7 mRNA for Prostate Cancer Prognosis Using an ISFET Lab-On-Chip Platform

被引:10
作者
Broomfield, Joseph [1 ,2 ]
Kalofonou, Melpomeni [1 ]
Pataillot-Meakin, Thomas [2 ,3 ]
Powell, Sue M. [2 ]
Fernandes, Rayzel C. [2 ]
Moser, Nicolas [1 ]
Bevan, Charlotte L. [2 ]
Georgiou, Pantelis [1 ]
机构
[1] Imperial Coll London, Ctr Bioinspired Technol, Dept Elect & Elect Engn, London SW7 2AZ, England
[2] Imperial Coll London, Imperial Ctr Translat & Expt Med, Dept Surg & Canc, London W12 0NN, England
[3] Imperial Coll London, Dept Bioengn & Mol Sci Res Hub, Dept Chem, Sir Michael Uren Hub, London W12 0BZ, England
关键词
prostate cancer; lab-on-chip; point-of-care device; RT-LAMP; AR-V7 and YAP1 RNA; ISFETs; sensors; REAL-TIME; MESENCHYMAL TRANSITION; RAPID DETECTION; AMPLIFICATION; DNA; ABIRATERONE; MICRORNA; PATHWAY;
D O I
10.1021/acssensors.2c01463
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Prostate cancer (PCa) is the second most common cause of male cancer-related death worldwide. The gold standard of treatment for advanced PCa is androgen deprivation therapy (ADT). However, eventual failure of ADT is common and leads to lethal metastatic castration-resistant PCa. As such, the detection of relevant biomarkers in the blood for drug resistance in metastatic castration-resistant PCa patients could lead to personalized treatment options. mRNA detection is often limited by the low specificity of qPCR assays which are restricted to specialized laboratories. Here, we present a novel reverse-transcription loop-mediated isothermal amplification assay and have demonstrated its capability for sensitive detection of AR-V7 and YAP1 RNA (3 x 101 RNA copies per reaction). This work presents a foundation for the detection of circulating mRNA in PCa on a non-invasive lab-on-chip device for use at the point-of-care. This technique was implemented onto a lab-on-chip platform integrating an array of chemical sensors (ion-sensitive field-effect transistors) for real-time detection of RNA. Detection of RNA presence was achieved through the translation of chemical signals into electrical readouts. Validation of this technique was conducted with rapid detection (<15 min) of extracted RNA from prostate cancer cell lines 22Rv1s and DU145s.
引用
收藏
页码:3389 / 3398
页数:10
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