Your browser doesn't support javascript.
loading
Detection of YAP1 and AR-V7 mRNA for Prostate Cancer Prognosis Using an ISFET Lab-On-Chip Platform.
Broomfield, Joseph; Kalofonou, Melpomeni; Pataillot-Meakin, Thomas; Powell, Sue M; Fernandes, Rayzel C; Moser, Nicolas; Bevan, Charlotte L; Georgiou, Pantelis.
Afiliación
  • Broomfield J; Centre for Bio-Inspired Technology, Department of Electrical and Electronic Engineering, Imperial College London, LondonSW7 2AZ, U.K.
  • Kalofonou M; Imperial Centre for Translational and Experimental Medicine, Department of Surgery and Cancer, Imperial College London, LondonW12 0NN, U.K.
  • Pataillot-Meakin T; Centre for Bio-Inspired Technology, Department of Electrical and Electronic Engineering, Imperial College London, LondonSW7 2AZ, U.K.
  • Powell SM; Imperial Centre for Translational and Experimental Medicine, Department of Surgery and Cancer, Imperial College London, LondonW12 0NN, U.K.
  • Fernandes RC; Sir Michael Uren Hub, Department of Bioengineering, Imperial College London, LondonW12 0BZ, U.K.
  • Moser N; Molecular Science Research Hub, Department of Chemistry, Imperial College London, LondonW12 0BZ, U.K.
  • Bevan CL; Imperial Centre for Translational and Experimental Medicine, Department of Surgery and Cancer, Imperial College London, LondonW12 0NN, U.K.
  • Georgiou P; Imperial Centre for Translational and Experimental Medicine, Department of Surgery and Cancer, Imperial College London, LondonW12 0NN, U.K.
ACS Sens ; 7(11): 3389-3398, 2022 11 25.
Article en En | MEDLINE | ID: mdl-36368032
ABSTRACT
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 × 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.
Asunto(s)
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias de la Próstata Resistentes a la Castración Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans / Male Idioma: En Revista: ACS Sens Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias de la Próstata Resistentes a la Castración Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans / Male Idioma: En Revista: ACS Sens Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido