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Detection of YAP1 and AR-V7 mRNA for Prostate Cancer Prognosis Using an ISFET Lab-On-Chip Platform
[Image: see text] 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. A...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9706784/ https://www.ncbi.nlm.nih.gov/pubmed/36368032 http://dx.doi.org/10.1021/acssensors.2c01463 |
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author | Broomfield, Joseph Kalofonou, Melpomeni Pataillot-Meakin, Thomas Powell, Sue M. Fernandes, Rayzel C. Moser, Nicolas Bevan, Charlotte L. Georgiou, Pantelis |
author_facet | Broomfield, Joseph Kalofonou, Melpomeni Pataillot-Meakin, Thomas Powell, Sue M. Fernandes, Rayzel C. Moser, Nicolas Bevan, Charlotte L. Georgiou, Pantelis |
author_sort | Broomfield, Joseph |
collection | PubMed |
description | [Image: see text] 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. |
format | Online Article Text |
id | pubmed-9706784 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-97067842022-11-30 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 ACS Sens [Image: see text] 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. American Chemical Society 2022-11-11 2022-11-25 /pmc/articles/PMC9706784/ /pubmed/36368032 http://dx.doi.org/10.1021/acssensors.2c01463 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Broomfield, Joseph Kalofonou, Melpomeni Pataillot-Meakin, Thomas Powell, Sue M. Fernandes, Rayzel C. Moser, Nicolas Bevan, Charlotte L. Georgiou, Pantelis Detection of YAP1 and AR-V7 mRNA for Prostate Cancer Prognosis Using an ISFET Lab-On-Chip Platform |
title | Detection of
YAP1 and AR-V7 mRNA for Prostate Cancer
Prognosis Using an ISFET Lab-On-Chip Platform |
title_full | Detection of
YAP1 and AR-V7 mRNA for Prostate Cancer
Prognosis Using an ISFET Lab-On-Chip Platform |
title_fullStr | Detection of
YAP1 and AR-V7 mRNA for Prostate Cancer
Prognosis Using an ISFET Lab-On-Chip Platform |
title_full_unstemmed | Detection of
YAP1 and AR-V7 mRNA for Prostate Cancer
Prognosis Using an ISFET Lab-On-Chip Platform |
title_short | Detection of
YAP1 and AR-V7 mRNA for Prostate Cancer
Prognosis Using an ISFET Lab-On-Chip Platform |
title_sort | detection of
yap1 and ar-v7 mrna for prostate cancer
prognosis using an isfet lab-on-chip platform |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9706784/ https://www.ncbi.nlm.nih.gov/pubmed/36368032 http://dx.doi.org/10.1021/acssensors.2c01463 |
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