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A dual biomarker detection platform for quantitating circulating tumor DNA (ctDNA)
Circulating tumor DNA (ctDNA), which includes DNA mutations, epigenetic alterations and other forms of tumor-specific abnormalities, is a promising “real-time” biomarker for noninvasive cancer assessment. Tumor DNA is of great value in the process of cancer treatment, including diagnostic and progno...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5743835/ https://www.ncbi.nlm.nih.gov/pubmed/29291160 http://dx.doi.org/10.7150/ntno.22419 |
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author | Cai, Chunyan Guo, Zhenzhong Cao, Yiping Zhang, Weiying Chen, Yong |
author_facet | Cai, Chunyan Guo, Zhenzhong Cao, Yiping Zhang, Weiying Chen, Yong |
author_sort | Cai, Chunyan |
collection | PubMed |
description | Circulating tumor DNA (ctDNA), which includes DNA mutations, epigenetic alterations and other forms of tumor-specific abnormalities, is a promising “real-time” biomarker for noninvasive cancer assessment. Tumor DNA is of great value in the process of cancer treatment, including diagnostic and prognostic information before, during treatment and at progression. Here we introduce a peptide nucleic acids probe-gold nanoparticles (PNA-AuNPs) and lead phosphate apoferritin (LPA)-based dual biomarker detection platform, which could be used in a DNA biosensor to quantify ctDNA by detection of tumor-specific mutations and methylation of PIK3CA gene. On the one hand, PNA probe and anti-5-Methylcytosine monoclonal antibody (anti-5-mC) were used to recognize the different parts of ctDNA, forming a sandwich-structure on a screen-printed electrode (SPE) surface. On the other hand, AuNPs and LPA were introduced to construct the biosensor for double signal amplification. Square-wave voltammetry (SWV) was used to monitor the electrochemical signal of lead ions released from apoferritin. The proposed DNA biosensor yielded a linear current response to ctDNA concentrations over a broad range of 50-10000 fM with a detection limit of 10 fM. It also successfully detected ctDNA collected from cancer patient serum. Therefore, we anticipate this new platform opens up an approach to detect and monitor diverse malignancies, facilitating personalized cancer therapy. |
format | Online Article Text |
id | pubmed-5743835 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-57438352018-01-01 A dual biomarker detection platform for quantitating circulating tumor DNA (ctDNA) Cai, Chunyan Guo, Zhenzhong Cao, Yiping Zhang, Weiying Chen, Yong Nanotheranostics Research Paper Circulating tumor DNA (ctDNA), which includes DNA mutations, epigenetic alterations and other forms of tumor-specific abnormalities, is a promising “real-time” biomarker for noninvasive cancer assessment. Tumor DNA is of great value in the process of cancer treatment, including diagnostic and prognostic information before, during treatment and at progression. Here we introduce a peptide nucleic acids probe-gold nanoparticles (PNA-AuNPs) and lead phosphate apoferritin (LPA)-based dual biomarker detection platform, which could be used in a DNA biosensor to quantify ctDNA by detection of tumor-specific mutations and methylation of PIK3CA gene. On the one hand, PNA probe and anti-5-Methylcytosine monoclonal antibody (anti-5-mC) were used to recognize the different parts of ctDNA, forming a sandwich-structure on a screen-printed electrode (SPE) surface. On the other hand, AuNPs and LPA were introduced to construct the biosensor for double signal amplification. Square-wave voltammetry (SWV) was used to monitor the electrochemical signal of lead ions released from apoferritin. The proposed DNA biosensor yielded a linear current response to ctDNA concentrations over a broad range of 50-10000 fM with a detection limit of 10 fM. It also successfully detected ctDNA collected from cancer patient serum. Therefore, we anticipate this new platform opens up an approach to detect and monitor diverse malignancies, facilitating personalized cancer therapy. Ivyspring International Publisher 2018-01-01 /pmc/articles/PMC5743835/ /pubmed/29291160 http://dx.doi.org/10.7150/ntno.22419 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Cai, Chunyan Guo, Zhenzhong Cao, Yiping Zhang, Weiying Chen, Yong A dual biomarker detection platform for quantitating circulating tumor DNA (ctDNA) |
title | A dual biomarker detection platform for quantitating circulating tumor DNA (ctDNA) |
title_full | A dual biomarker detection platform for quantitating circulating tumor DNA (ctDNA) |
title_fullStr | A dual biomarker detection platform for quantitating circulating tumor DNA (ctDNA) |
title_full_unstemmed | A dual biomarker detection platform for quantitating circulating tumor DNA (ctDNA) |
title_short | A dual biomarker detection platform for quantitating circulating tumor DNA (ctDNA) |
title_sort | dual biomarker detection platform for quantitating circulating tumor dna (ctdna) |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5743835/ https://www.ncbi.nlm.nih.gov/pubmed/29291160 http://dx.doi.org/10.7150/ntno.22419 |
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