Detection of YAP1 and AR-V7 mRNA for Prostate Cancer Prognosis Using an ISFET Lab-On-Chip Platform.
Joseph BroomfieldMelpomeni KalofonouThomas Pataillot-MeakinSue M PowellRayzel C FernandesNicolas MoserCharlotte Lynne BevanPantelis GeorgiouPublished in: ACS sensors (2022)
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 × 10 1 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.
Keyphrases
- loop mediated isothermal amplification
- sensitive detection
- prostate cancer
- high throughput
- label free
- small cell lung cancer
- squamous cell carcinoma
- radical prostatectomy
- stem cells
- newly diagnosed
- end stage renal disease
- chronic kidney disease
- quantum dots
- palliative care
- transcription factor
- circulating tumor cells
- ejection fraction
- single cell
- prognostic factors
- smoking cessation
- binding protein