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Ratiometric electrochemical OR gate assay for NSCLC-derived exosomes

Non-small cell lung cancer (NSCLC) is the most common pathological type of LC and ranks as the leading cause of cancer deaths. Circulating exosomes have emerged as a valuable biomarker for the diagnosis of NSCLC, while the performance of current electrochemical assays for exosome detection is constr...

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Autores principales: Meng, Fanyu, Yu, Wenjun, Niu, Minjia, Tian, Xiaoting, Miao, Yayou, Li, Xvelian, Zhou, Yan, Ma, Lifang, Zhang, Xiao, Qian, Kun, Yu, Yongchun, Wang, Jiayi, Huang, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10037838/
https://www.ncbi.nlm.nih.gov/pubmed/36964516
http://dx.doi.org/10.1186/s12951-023-01833-2
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author Meng, Fanyu
Yu, Wenjun
Niu, Minjia
Tian, Xiaoting
Miao, Yayou
Li, Xvelian
Zhou, Yan
Ma, Lifang
Zhang, Xiao
Qian, Kun
Yu, Yongchun
Wang, Jiayi
Huang, Lin
author_facet Meng, Fanyu
Yu, Wenjun
Niu, Minjia
Tian, Xiaoting
Miao, Yayou
Li, Xvelian
Zhou, Yan
Ma, Lifang
Zhang, Xiao
Qian, Kun
Yu, Yongchun
Wang, Jiayi
Huang, Lin
author_sort Meng, Fanyu
collection PubMed
description Non-small cell lung cancer (NSCLC) is the most common pathological type of LC and ranks as the leading cause of cancer deaths. Circulating exosomes have emerged as a valuable biomarker for the diagnosis of NSCLC, while the performance of current electrochemical assays for exosome detection is constrained by unsatisfactory sensitivity and specificity. Here we integrated a ratiometric biosensor with an OR logic gate to form an assay for surface protein profiling of exosomes from clinical serum samples. By using the specific aptamers for recognition of clinically validated biomarkers (EpCAM and CEA), the assay enabled ultrasensitive detection of trace levels of NSCLC-derived exosomes in complex serum samples (15.1 particles μL(−1) within a linear range of 10(2)–10(8) particles μL(−1)). The assay outperformed the analysis of six serum biomarkers for the accurate diagnosis, staging, and prognosis of NSCLC, displaying a diagnostic sensitivity of 93.3% even at an early stage (Stage I). The assay provides an advanced tool for exosome quantification and facilitates exosome-based liquid biopsies for cancer management in clinics. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-023-01833-2.
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spelling pubmed-100378382023-03-25 Ratiometric electrochemical OR gate assay for NSCLC-derived exosomes Meng, Fanyu Yu, Wenjun Niu, Minjia Tian, Xiaoting Miao, Yayou Li, Xvelian Zhou, Yan Ma, Lifang Zhang, Xiao Qian, Kun Yu, Yongchun Wang, Jiayi Huang, Lin J Nanobiotechnology Research Non-small cell lung cancer (NSCLC) is the most common pathological type of LC and ranks as the leading cause of cancer deaths. Circulating exosomes have emerged as a valuable biomarker for the diagnosis of NSCLC, while the performance of current electrochemical assays for exosome detection is constrained by unsatisfactory sensitivity and specificity. Here we integrated a ratiometric biosensor with an OR logic gate to form an assay for surface protein profiling of exosomes from clinical serum samples. By using the specific aptamers for recognition of clinically validated biomarkers (EpCAM and CEA), the assay enabled ultrasensitive detection of trace levels of NSCLC-derived exosomes in complex serum samples (15.1 particles μL(−1) within a linear range of 10(2)–10(8) particles μL(−1)). The assay outperformed the analysis of six serum biomarkers for the accurate diagnosis, staging, and prognosis of NSCLC, displaying a diagnostic sensitivity of 93.3% even at an early stage (Stage I). The assay provides an advanced tool for exosome quantification and facilitates exosome-based liquid biopsies for cancer management in clinics. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-023-01833-2. BioMed Central 2023-03-24 /pmc/articles/PMC10037838/ /pubmed/36964516 http://dx.doi.org/10.1186/s12951-023-01833-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Meng, Fanyu
Yu, Wenjun
Niu, Minjia
Tian, Xiaoting
Miao, Yayou
Li, Xvelian
Zhou, Yan
Ma, Lifang
Zhang, Xiao
Qian, Kun
Yu, Yongchun
Wang, Jiayi
Huang, Lin
Ratiometric electrochemical OR gate assay for NSCLC-derived exosomes
title Ratiometric electrochemical OR gate assay for NSCLC-derived exosomes
title_full Ratiometric electrochemical OR gate assay for NSCLC-derived exosomes
title_fullStr Ratiometric electrochemical OR gate assay for NSCLC-derived exosomes
title_full_unstemmed Ratiometric electrochemical OR gate assay for NSCLC-derived exosomes
title_short Ratiometric electrochemical OR gate assay for NSCLC-derived exosomes
title_sort ratiometric electrochemical or gate assay for nsclc-derived exosomes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10037838/
https://www.ncbi.nlm.nih.gov/pubmed/36964516
http://dx.doi.org/10.1186/s12951-023-01833-2
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