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Miniaturized microfluidic-based nucleic acid analyzer to identify new biomarkers of biopsy lung cancer samples for subtyping

Identifying new biomarkers is necessary and important to diagnose and treat malignant lung cancer. However, existing protein marker detection methods usually require complex operation steps, leading to a lag time for diagnosis. Herein, we developed a rapid, minimally invasive, and convenient nucleic...

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Autores principales: Lin, Xue, Bo, Zi-Hao, Lv, Wenqi, Zhou, Zhanping, Huang, Qin, Du, Wenli, Shan, Xiaohui, Fu, Rongxin, Jin, Xiangyu, Yang, Han, Su, Ya, Jiang, Kai, Guo, Yuchen, Wang, Hongwu, Xu, Feng, Huang, Guoliang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9466282/
https://www.ncbi.nlm.nih.gov/pubmed/36105308
http://dx.doi.org/10.3389/fchem.2022.946157
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author Lin, Xue
Bo, Zi-Hao
Lv, Wenqi
Zhou, Zhanping
Huang, Qin
Du, Wenli
Shan, Xiaohui
Fu, Rongxin
Jin, Xiangyu
Yang, Han
Su, Ya
Jiang, Kai
Guo, Yuchen
Wang, Hongwu
Xu, Feng
Huang, Guoliang
author_facet Lin, Xue
Bo, Zi-Hao
Lv, Wenqi
Zhou, Zhanping
Huang, Qin
Du, Wenli
Shan, Xiaohui
Fu, Rongxin
Jin, Xiangyu
Yang, Han
Su, Ya
Jiang, Kai
Guo, Yuchen
Wang, Hongwu
Xu, Feng
Huang, Guoliang
author_sort Lin, Xue
collection PubMed
description Identifying new biomarkers is necessary and important to diagnose and treat malignant lung cancer. However, existing protein marker detection methods usually require complex operation steps, leading to a lag time for diagnosis. Herein, we developed a rapid, minimally invasive, and convenient nucleic acid biomarker recognition method, which enabled the combined specific detection of 11 lung cancer typing markers in a microliter reaction system after only one sampling. The primers for the combined specific detection of 11 lung cancer typing markers were designed and screened, and the microfluidic chip for parallel detection of the multiple markers was designed and developed. Furthermore, a miniaturized microfluidic-based analyzer was also constructed. By developing a microfluidic chip and a miniaturized nucleic acid analyzer, we enabled the detection of the mRNA expression levels of multiple biomarkers in rice-sized tissue samples. The miniaturized nucleic acid analyzer could detect ≥10 copies of nucleic acids. The cell volume of the typing reaction on the microfluidic chip was only 0.94 μL, less than 1/25 of that of the conventional 25-μL Eppendorf tube PCR method, which significantly reduced the testing cost and significantly simplified the analysis of multiple biomarkers in parallel. With a simple injection operation and reverse transcription loop-mediated isothermal amplification (RT-LAMP), real-time detection of 11 lung cancer nucleic acid biomarkers was performed within 45 min. Given these compelling features, 86 clinical samples were tested using the miniaturized nucleic acid analyzer and classified according to the cutoff values of the 11 biomarkers. Furthermore, multi-biomarker analysis was conducted by a machine learning model to classify different subtypes of lung cancer, with an average area under the curve (AUC) of 0.934. This method shows great potential for the identification of new nucleic acid biomarkers and the accurate diagnosis of lung cancer.
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spelling pubmed-94662822022-09-13 Miniaturized microfluidic-based nucleic acid analyzer to identify new biomarkers of biopsy lung cancer samples for subtyping Lin, Xue Bo, Zi-Hao Lv, Wenqi Zhou, Zhanping Huang, Qin Du, Wenli Shan, Xiaohui Fu, Rongxin Jin, Xiangyu Yang, Han Su, Ya Jiang, Kai Guo, Yuchen Wang, Hongwu Xu, Feng Huang, Guoliang Front Chem Chemistry Identifying new biomarkers is necessary and important to diagnose and treat malignant lung cancer. However, existing protein marker detection methods usually require complex operation steps, leading to a lag time for diagnosis. Herein, we developed a rapid, minimally invasive, and convenient nucleic acid biomarker recognition method, which enabled the combined specific detection of 11 lung cancer typing markers in a microliter reaction system after only one sampling. The primers for the combined specific detection of 11 lung cancer typing markers were designed and screened, and the microfluidic chip for parallel detection of the multiple markers was designed and developed. Furthermore, a miniaturized microfluidic-based analyzer was also constructed. By developing a microfluidic chip and a miniaturized nucleic acid analyzer, we enabled the detection of the mRNA expression levels of multiple biomarkers in rice-sized tissue samples. The miniaturized nucleic acid analyzer could detect ≥10 copies of nucleic acids. The cell volume of the typing reaction on the microfluidic chip was only 0.94 μL, less than 1/25 of that of the conventional 25-μL Eppendorf tube PCR method, which significantly reduced the testing cost and significantly simplified the analysis of multiple biomarkers in parallel. With a simple injection operation and reverse transcription loop-mediated isothermal amplification (RT-LAMP), real-time detection of 11 lung cancer nucleic acid biomarkers was performed within 45 min. Given these compelling features, 86 clinical samples were tested using the miniaturized nucleic acid analyzer and classified according to the cutoff values of the 11 biomarkers. Furthermore, multi-biomarker analysis was conducted by a machine learning model to classify different subtypes of lung cancer, with an average area under the curve (AUC) of 0.934. This method shows great potential for the identification of new nucleic acid biomarkers and the accurate diagnosis of lung cancer. Frontiers Media S.A. 2022-08-29 /pmc/articles/PMC9466282/ /pubmed/36105308 http://dx.doi.org/10.3389/fchem.2022.946157 Text en Copyright © 2022 Lin, Bo, Lv, Zhou, Huang, Du, Shan, Fu, Jin, Yang, Su, Jiang, Guo, Wang, Xu and Huang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Chemistry
Lin, Xue
Bo, Zi-Hao
Lv, Wenqi
Zhou, Zhanping
Huang, Qin
Du, Wenli
Shan, Xiaohui
Fu, Rongxin
Jin, Xiangyu
Yang, Han
Su, Ya
Jiang, Kai
Guo, Yuchen
Wang, Hongwu
Xu, Feng
Huang, Guoliang
Miniaturized microfluidic-based nucleic acid analyzer to identify new biomarkers of biopsy lung cancer samples for subtyping
title Miniaturized microfluidic-based nucleic acid analyzer to identify new biomarkers of biopsy lung cancer samples for subtyping
title_full Miniaturized microfluidic-based nucleic acid analyzer to identify new biomarkers of biopsy lung cancer samples for subtyping
title_fullStr Miniaturized microfluidic-based nucleic acid analyzer to identify new biomarkers of biopsy lung cancer samples for subtyping
title_full_unstemmed Miniaturized microfluidic-based nucleic acid analyzer to identify new biomarkers of biopsy lung cancer samples for subtyping
title_short Miniaturized microfluidic-based nucleic acid analyzer to identify new biomarkers of biopsy lung cancer samples for subtyping
title_sort miniaturized microfluidic-based nucleic acid analyzer to identify new biomarkers of biopsy lung cancer samples for subtyping
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9466282/
https://www.ncbi.nlm.nih.gov/pubmed/36105308
http://dx.doi.org/10.3389/fchem.2022.946157
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