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Multiplex Digital Methylation‐Specific PCR for Noninvasive Screening of Lung Cancer

There remains tremendous interest in developing liquid biopsy assays for detection of cancer‐specific alterations, such as mutations and DNA methylation, in cell‐free DNA (cfDNA) obtained through noninvasive blood draws. However, liquid biopsy analysis is often challenging due to exceedingly low fra...

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Autores principales: Zhao, Yang, O'Keefe, Christine M., Hsieh, Kuangwen, Cope, Leslie, Joyce, Sonali C., Pisanic, Thomas R., Herman, James G., Wang, Tza‐Huei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10238189/
https://www.ncbi.nlm.nih.gov/pubmed/37039321
http://dx.doi.org/10.1002/advs.202206518
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author Zhao, Yang
O'Keefe, Christine M.
Hsieh, Kuangwen
Cope, Leslie
Joyce, Sonali C.
Pisanic, Thomas R.
Herman, James G.
Wang, Tza‐Huei
author_facet Zhao, Yang
O'Keefe, Christine M.
Hsieh, Kuangwen
Cope, Leslie
Joyce, Sonali C.
Pisanic, Thomas R.
Herman, James G.
Wang, Tza‐Huei
author_sort Zhao, Yang
collection PubMed
description There remains tremendous interest in developing liquid biopsy assays for detection of cancer‐specific alterations, such as mutations and DNA methylation, in cell‐free DNA (cfDNA) obtained through noninvasive blood draws. However, liquid biopsy analysis is often challenging due to exceedingly low fractions of circulating tumor DNA (ctDNA), necessitating the use of extended tumor biomarker panels. While multiplexed PCR strategies provide advantages such as higher throughput, their implementation is often hindered by challenges such as primer‐dimers and PCR competition. Alternatively, digital PCR (dPCR) approaches generally offer superior performance, but with constrained multiplexing capability. This paper describes development and validation of the first multiplex digital methylation‐specific PCR (mdMSP) platform for simultaneous analysis of four methylation biomarkers for liquid‐biopsy‐based detection of non‐small cell lung cancer (NSCLC). mdMSP employs a microfluidic device containing four independent, but identical modules, housing a total of 40 160 nanowells. Analytical validation of the mdMSP platform demonstrates multiplex detection at analytical specificities as low as 0.0005%. The clinical utility of mdMSP is also demonstrated in a cohort of 72 clinical samples of low‐volume liquid biopsy specimens from patients with computed tomography (CT)‐scan indeterminant pulmonary nodules, exhibiting superior clinical performance when compared to traditional MSP assays for noninvasive detection of early‐stage NSCLC.
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spelling pubmed-102381892023-06-04 Multiplex Digital Methylation‐Specific PCR for Noninvasive Screening of Lung Cancer Zhao, Yang O'Keefe, Christine M. Hsieh, Kuangwen Cope, Leslie Joyce, Sonali C. Pisanic, Thomas R. Herman, James G. Wang, Tza‐Huei Adv Sci (Weinh) Research Articles There remains tremendous interest in developing liquid biopsy assays for detection of cancer‐specific alterations, such as mutations and DNA methylation, in cell‐free DNA (cfDNA) obtained through noninvasive blood draws. However, liquid biopsy analysis is often challenging due to exceedingly low fractions of circulating tumor DNA (ctDNA), necessitating the use of extended tumor biomarker panels. While multiplexed PCR strategies provide advantages such as higher throughput, their implementation is often hindered by challenges such as primer‐dimers and PCR competition. Alternatively, digital PCR (dPCR) approaches generally offer superior performance, but with constrained multiplexing capability. This paper describes development and validation of the first multiplex digital methylation‐specific PCR (mdMSP) platform for simultaneous analysis of four methylation biomarkers for liquid‐biopsy‐based detection of non‐small cell lung cancer (NSCLC). mdMSP employs a microfluidic device containing four independent, but identical modules, housing a total of 40 160 nanowells. Analytical validation of the mdMSP platform demonstrates multiplex detection at analytical specificities as low as 0.0005%. The clinical utility of mdMSP is also demonstrated in a cohort of 72 clinical samples of low‐volume liquid biopsy specimens from patients with computed tomography (CT)‐scan indeterminant pulmonary nodules, exhibiting superior clinical performance when compared to traditional MSP assays for noninvasive detection of early‐stage NSCLC. John Wiley and Sons Inc. 2023-04-11 /pmc/articles/PMC10238189/ /pubmed/37039321 http://dx.doi.org/10.1002/advs.202206518 Text en © 2023 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Zhao, Yang
O'Keefe, Christine M.
Hsieh, Kuangwen
Cope, Leslie
Joyce, Sonali C.
Pisanic, Thomas R.
Herman, James G.
Wang, Tza‐Huei
Multiplex Digital Methylation‐Specific PCR for Noninvasive Screening of Lung Cancer
title Multiplex Digital Methylation‐Specific PCR for Noninvasive Screening of Lung Cancer
title_full Multiplex Digital Methylation‐Specific PCR for Noninvasive Screening of Lung Cancer
title_fullStr Multiplex Digital Methylation‐Specific PCR for Noninvasive Screening of Lung Cancer
title_full_unstemmed Multiplex Digital Methylation‐Specific PCR for Noninvasive Screening of Lung Cancer
title_short Multiplex Digital Methylation‐Specific PCR for Noninvasive Screening of Lung Cancer
title_sort multiplex digital methylation‐specific pcr for noninvasive screening of lung cancer
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10238189/
https://www.ncbi.nlm.nih.gov/pubmed/37039321
http://dx.doi.org/10.1002/advs.202206518
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