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Profiling Plasma Cytokines by A CRISPR-ELISA Assay for Early Detection of Lung Cancer
Cytokines play crucial roles in tumorigenesis and are potential biomarkers for cancer diagnosis. An Enzyme-linked Immunosorbent Assay (ELISA) is commonly used to measure cytokines but has a low sensitivity and can only detect a single target at a time. CRISPR-Associated Proteins (Cas) can ultra-sens...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9740838/ https://www.ncbi.nlm.nih.gov/pubmed/36498497 http://dx.doi.org/10.3390/jcm11236923 |
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author | Li, Ning Chinthalapally, Molangur Holden, Van K. Deepak, Janaki Dhilipkannah, Pushpa Fan, Jonathan M. Todd, Nevins W. Jiang, Feng |
author_facet | Li, Ning Chinthalapally, Molangur Holden, Van K. Deepak, Janaki Dhilipkannah, Pushpa Fan, Jonathan M. Todd, Nevins W. Jiang, Feng |
author_sort | Li, Ning |
collection | PubMed |
description | Cytokines play crucial roles in tumorigenesis and are potential biomarkers for cancer diagnosis. An Enzyme-linked Immunosorbent Assay (ELISA) is commonly used to measure cytokines but has a low sensitivity and can only detect a single target at a time. CRISPR-Associated Proteins (Cas) can ultra-sensitively and specifically detect nucleic acids and is revolutionizing molecular diagnostics. Here, we design a microplate-based CRISPR-ELISA assay to simultaneously profile multiple cytokines, in which antibodies are coupled with ssDNA to form antibody-ssDNA complexes that bridges CRISPR/Cas12a and ELISA reactions. The ssDNA triggers the Cas12a collateral cleavage activity and releases the fluorescent reporters to generate amplified fluorescent signals in the ELISA detection of cytokines. The CRISPR-ELISA assay can simultaneously measure multiple cytokines with a significantly higher sensitivity compared with conventional ELISA. Using the CRISPR-ELISA assay to profile plasma cytokines in 127 lung cancer patients and 125 cancer-free smokers, we develop a panel of plasma cytokine biomarkers (IL-6, IL-8, and IL-10) for early detection of the disease, with 80.6% sensitivity and 82.0% specificity. The CRISPR-ELISA assay may provide a new approach to the discovery of cytokine biomarkers for early lung cancer detection. |
format | Online Article Text |
id | pubmed-9740838 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-97408382022-12-11 Profiling Plasma Cytokines by A CRISPR-ELISA Assay for Early Detection of Lung Cancer Li, Ning Chinthalapally, Molangur Holden, Van K. Deepak, Janaki Dhilipkannah, Pushpa Fan, Jonathan M. Todd, Nevins W. Jiang, Feng J Clin Med Article Cytokines play crucial roles in tumorigenesis and are potential biomarkers for cancer diagnosis. An Enzyme-linked Immunosorbent Assay (ELISA) is commonly used to measure cytokines but has a low sensitivity and can only detect a single target at a time. CRISPR-Associated Proteins (Cas) can ultra-sensitively and specifically detect nucleic acids and is revolutionizing molecular diagnostics. Here, we design a microplate-based CRISPR-ELISA assay to simultaneously profile multiple cytokines, in which antibodies are coupled with ssDNA to form antibody-ssDNA complexes that bridges CRISPR/Cas12a and ELISA reactions. The ssDNA triggers the Cas12a collateral cleavage activity and releases the fluorescent reporters to generate amplified fluorescent signals in the ELISA detection of cytokines. The CRISPR-ELISA assay can simultaneously measure multiple cytokines with a significantly higher sensitivity compared with conventional ELISA. Using the CRISPR-ELISA assay to profile plasma cytokines in 127 lung cancer patients and 125 cancer-free smokers, we develop a panel of plasma cytokine biomarkers (IL-6, IL-8, and IL-10) for early detection of the disease, with 80.6% sensitivity and 82.0% specificity. The CRISPR-ELISA assay may provide a new approach to the discovery of cytokine biomarkers for early lung cancer detection. MDPI 2022-11-24 /pmc/articles/PMC9740838/ /pubmed/36498497 http://dx.doi.org/10.3390/jcm11236923 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Li, Ning Chinthalapally, Molangur Holden, Van K. Deepak, Janaki Dhilipkannah, Pushpa Fan, Jonathan M. Todd, Nevins W. Jiang, Feng Profiling Plasma Cytokines by A CRISPR-ELISA Assay for Early Detection of Lung Cancer |
title | Profiling Plasma Cytokines by A CRISPR-ELISA Assay for Early Detection of Lung Cancer |
title_full | Profiling Plasma Cytokines by A CRISPR-ELISA Assay for Early Detection of Lung Cancer |
title_fullStr | Profiling Plasma Cytokines by A CRISPR-ELISA Assay for Early Detection of Lung Cancer |
title_full_unstemmed | Profiling Plasma Cytokines by A CRISPR-ELISA Assay for Early Detection of Lung Cancer |
title_short | Profiling Plasma Cytokines by A CRISPR-ELISA Assay for Early Detection of Lung Cancer |
title_sort | profiling plasma cytokines by a crispr-elisa assay for early detection of lung cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9740838/ https://www.ncbi.nlm.nih.gov/pubmed/36498497 http://dx.doi.org/10.3390/jcm11236923 |
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