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Tissue microRNAs in non-small cell lung cancer detected with a new kind of liquid bead array detection system

BACKGROUND: Commonly used miRNA detection methods cannot be applied for high-throughput analyses. However, this study was aimed to performed a liquid bead array detection system (LBAS) to detect tissue 6 miRNAs in non-small cell lung cancer (NSCLC). METHODS: In this study, evaluation of LBAS was per...

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Autores principales: Zheng, Yuan-Yuan, Fei, Yun, Wang, Zheng, Chen, Yue, Qiu, Cheng, Li, Fu-Rong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7053089/
https://www.ncbi.nlm.nih.gov/pubmed/32122370
http://dx.doi.org/10.1186/s12967-020-02280-5
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author Zheng, Yuan-Yuan
Fei, Yun
Wang, Zheng
Chen, Yue
Qiu, Cheng
Li, Fu-Rong
author_facet Zheng, Yuan-Yuan
Fei, Yun
Wang, Zheng
Chen, Yue
Qiu, Cheng
Li, Fu-Rong
author_sort Zheng, Yuan-Yuan
collection PubMed
description BACKGROUND: Commonly used miRNA detection methods cannot be applied for high-throughput analyses. However, this study was aimed to performed a liquid bead array detection system (LBAS) to detect tissue 6 miRNAs in non-small cell lung cancer (NSCLC). METHODS: In this study, evaluation of LBAS was performed to observe the precision, specificity, limitation and stability. Then, a total of 52 primary NSCLC patients who received resection operation without preoperative radiotherapy and chemotherapy between June 2013 and March 2014 were selected, and then the total RNA of the tissues were extracted. We prepared six NSCLC-related miRNAs for LBAS. After optimization and evaluation, LBAS was verified by detecting the relative expression levels of 6 microRNAs in the pathological tissues and corresponding normal tissues of 52 NSCLC patients. RESULTS: The results of evaluation of LBAS showed that the Mean Fluorescence Intensity (MFI) of the reaction only added with chimeric probes and beads showed no significant change after 180 days (P > 0.05). And the intra-assay Coefficient of Variation (CV) was between 1.57 and 3.5%, while the inter-assay CV was between 4.24 and 11.27%, indicating this system was ideal for diagnostic reagents. In addition, only the beads corresponding to the additional miRNAs showed high MFIs from 8426 to 18,769, whereas the fluorescence values of the other beads were under background levels (MFIs = 20 to 55) in each reaction, indicating no cross reactivity among the miRNAs. The limit of detection of miR-21, miR-210, miR-125b, miR-155, miR-375, and miR-31 were 5.27, 1.39, 1.85, 2.01, 1.34, and 2.73 amol/μL, respectively, showing that the lowest detection limit of miRNA by this system was under pM level. Then, the relative expression levels of miR-21, miR-210, miR-125b, miR-155, miR-375, and miR-31 by using this system were significantly correlated with NSCLC (P < 0.05). And the results of AUC method indicated that specific of the LBAS system was 94.2%. CONCLUSIONS: Our findings suggest that LBAS was simple, high-throughput, and freely combined with absolute quantification. Thus, this system could be applied for tumor miRNAs detection.
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spelling pubmed-70530892020-03-10 Tissue microRNAs in non-small cell lung cancer detected with a new kind of liquid bead array detection system Zheng, Yuan-Yuan Fei, Yun Wang, Zheng Chen, Yue Qiu, Cheng Li, Fu-Rong J Transl Med Research BACKGROUND: Commonly used miRNA detection methods cannot be applied for high-throughput analyses. However, this study was aimed to performed a liquid bead array detection system (LBAS) to detect tissue 6 miRNAs in non-small cell lung cancer (NSCLC). METHODS: In this study, evaluation of LBAS was performed to observe the precision, specificity, limitation and stability. Then, a total of 52 primary NSCLC patients who received resection operation without preoperative radiotherapy and chemotherapy between June 2013 and March 2014 were selected, and then the total RNA of the tissues were extracted. We prepared six NSCLC-related miRNAs for LBAS. After optimization and evaluation, LBAS was verified by detecting the relative expression levels of 6 microRNAs in the pathological tissues and corresponding normal tissues of 52 NSCLC patients. RESULTS: The results of evaluation of LBAS showed that the Mean Fluorescence Intensity (MFI) of the reaction only added with chimeric probes and beads showed no significant change after 180 days (P > 0.05). And the intra-assay Coefficient of Variation (CV) was between 1.57 and 3.5%, while the inter-assay CV was between 4.24 and 11.27%, indicating this system was ideal for diagnostic reagents. In addition, only the beads corresponding to the additional miRNAs showed high MFIs from 8426 to 18,769, whereas the fluorescence values of the other beads were under background levels (MFIs = 20 to 55) in each reaction, indicating no cross reactivity among the miRNAs. The limit of detection of miR-21, miR-210, miR-125b, miR-155, miR-375, and miR-31 were 5.27, 1.39, 1.85, 2.01, 1.34, and 2.73 amol/μL, respectively, showing that the lowest detection limit of miRNA by this system was under pM level. Then, the relative expression levels of miR-21, miR-210, miR-125b, miR-155, miR-375, and miR-31 by using this system were significantly correlated with NSCLC (P < 0.05). And the results of AUC method indicated that specific of the LBAS system was 94.2%. CONCLUSIONS: Our findings suggest that LBAS was simple, high-throughput, and freely combined with absolute quantification. Thus, this system could be applied for tumor miRNAs detection. BioMed Central 2020-03-02 /pmc/articles/PMC7053089/ /pubmed/32122370 http://dx.doi.org/10.1186/s12967-020-02280-5 Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://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
Zheng, Yuan-Yuan
Fei, Yun
Wang, Zheng
Chen, Yue
Qiu, Cheng
Li, Fu-Rong
Tissue microRNAs in non-small cell lung cancer detected with a new kind of liquid bead array detection system
title Tissue microRNAs in non-small cell lung cancer detected with a new kind of liquid bead array detection system
title_full Tissue microRNAs in non-small cell lung cancer detected with a new kind of liquid bead array detection system
title_fullStr Tissue microRNAs in non-small cell lung cancer detected with a new kind of liquid bead array detection system
title_full_unstemmed Tissue microRNAs in non-small cell lung cancer detected with a new kind of liquid bead array detection system
title_short Tissue microRNAs in non-small cell lung cancer detected with a new kind of liquid bead array detection system
title_sort tissue micrornas in non-small cell lung cancer detected with a new kind of liquid bead array detection system
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7053089/
https://www.ncbi.nlm.nih.gov/pubmed/32122370
http://dx.doi.org/10.1186/s12967-020-02280-5
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