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Plasma extracellular vesicle microRNA profiling and the identification of a diagnostic signature for stage I lung adenocarcinoma
At present, there is no effective noninvasive method for the accurate diagnosis of early‐stage lung adenocarcinoma (LUAD). This study examined the profile of plasma extracellular vesicle (EV)‐delivered microRNAs (miRNAs) in patients with invasive stage I LUAD. In this study, a total of 460 participa...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8819331/ https://www.ncbi.nlm.nih.gov/pubmed/34837453 http://dx.doi.org/10.1111/cas.15222 |
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author | Gao, Shugeng Guo, Wei Liu, Tiejun Liang, Naixin Ma, Qianli Gao, Yibo Tan, Fengwei Xue, Qi He, Jie |
author_facet | Gao, Shugeng Guo, Wei Liu, Tiejun Liang, Naixin Ma, Qianli Gao, Yibo Tan, Fengwei Xue, Qi He, Jie |
author_sort | Gao, Shugeng |
collection | PubMed |
description | At present, there is no effective noninvasive method for the accurate diagnosis of early‐stage lung adenocarcinoma (LUAD). This study examined the profile of plasma extracellular vesicle (EV)‐delivered microRNAs (miRNAs) in patients with invasive stage I LUAD. In this study, a total of 460 participants were enrolled, including 254 patients with LUAD, 76 patients with benign pulmonary nodules (BPNs), and 130 healthy control patients (HCs). miRNA sequencing was used to analyze the EV miRNA profile of the patient plasma samples (n = 150). A diagnostic signature (d‐signature) was identified by applying a stepwise logistic regression algorithm, and a single‐center training cohort (n = 150) was tested, followed by a multicenter validation cohort (n = 100). A d‐signature comprising four EV‐derived miRNAs (hsa‐miR‐106b‐3p, hsa‐miR‐125a‐5p, hsa‐miR‐3615, and hsa‐miR‐450b‐5p) was developed for the early detection of LUAD. The d‐signature had high precision with area under the curve (AUC) values of 0.917 and 0.902 in the training and test cohorts, respectively. Moreover, the d‐signature could recognize patients with adenocarcinoma in situ (AIS) and minimally invasive adenocarcinoma (MIA) with AUC values of 0.846 and 0.92, respectively. To sum up, our study detailed the plasma EV–derived miRNA profile in early LUAD patients and developed an EV‐derived miRNA d‐signature to detect early LUAD. |
format | Online Article Text |
id | pubmed-8819331 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-88193312022-02-11 Plasma extracellular vesicle microRNA profiling and the identification of a diagnostic signature for stage I lung adenocarcinoma Gao, Shugeng Guo, Wei Liu, Tiejun Liang, Naixin Ma, Qianli Gao, Yibo Tan, Fengwei Xue, Qi He, Jie Cancer Sci Original Articles At present, there is no effective noninvasive method for the accurate diagnosis of early‐stage lung adenocarcinoma (LUAD). This study examined the profile of plasma extracellular vesicle (EV)‐delivered microRNAs (miRNAs) in patients with invasive stage I LUAD. In this study, a total of 460 participants were enrolled, including 254 patients with LUAD, 76 patients with benign pulmonary nodules (BPNs), and 130 healthy control patients (HCs). miRNA sequencing was used to analyze the EV miRNA profile of the patient plasma samples (n = 150). A diagnostic signature (d‐signature) was identified by applying a stepwise logistic regression algorithm, and a single‐center training cohort (n = 150) was tested, followed by a multicenter validation cohort (n = 100). A d‐signature comprising four EV‐derived miRNAs (hsa‐miR‐106b‐3p, hsa‐miR‐125a‐5p, hsa‐miR‐3615, and hsa‐miR‐450b‐5p) was developed for the early detection of LUAD. The d‐signature had high precision with area under the curve (AUC) values of 0.917 and 0.902 in the training and test cohorts, respectively. Moreover, the d‐signature could recognize patients with adenocarcinoma in situ (AIS) and minimally invasive adenocarcinoma (MIA) with AUC values of 0.846 and 0.92, respectively. To sum up, our study detailed the plasma EV–derived miRNA profile in early LUAD patients and developed an EV‐derived miRNA d‐signature to detect early LUAD. John Wiley and Sons Inc. 2021-12-06 2022-02 /pmc/articles/PMC8819331/ /pubmed/34837453 http://dx.doi.org/10.1111/cas.15222 Text en © 2021 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Gao, Shugeng Guo, Wei Liu, Tiejun Liang, Naixin Ma, Qianli Gao, Yibo Tan, Fengwei Xue, Qi He, Jie Plasma extracellular vesicle microRNA profiling and the identification of a diagnostic signature for stage I lung adenocarcinoma |
title | Plasma extracellular vesicle microRNA profiling and the identification of a diagnostic signature for stage I lung adenocarcinoma |
title_full | Plasma extracellular vesicle microRNA profiling and the identification of a diagnostic signature for stage I lung adenocarcinoma |
title_fullStr | Plasma extracellular vesicle microRNA profiling and the identification of a diagnostic signature for stage I lung adenocarcinoma |
title_full_unstemmed | Plasma extracellular vesicle microRNA profiling and the identification of a diagnostic signature for stage I lung adenocarcinoma |
title_short | Plasma extracellular vesicle microRNA profiling and the identification of a diagnostic signature for stage I lung adenocarcinoma |
title_sort | plasma extracellular vesicle microrna profiling and the identification of a diagnostic signature for stage i lung adenocarcinoma |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8819331/ https://www.ncbi.nlm.nih.gov/pubmed/34837453 http://dx.doi.org/10.1111/cas.15222 |
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