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Identification and Characterization of Extrachromosomal Circular DNA in Plasma of Lung Adenocarcinoma Patients

BACKGROUND: Chromosome is the basic framework for eukaryotic cells to store genetic information, but certain genes exist in circulation, such as extrachromosomal circular DNA (eccDNA). The unique genetic characteristics and structure of eccDNA provide a new vision on the early diagnosis of cancer; h...

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Autores principales: Wu, Xiaoqiong, Li, Pu, Yimiti, Maimaitiaili, Ye, Zhiqiu, Fang, Xuqian, Chen, Peizhan, Gu, Zhidong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9113459/
https://www.ncbi.nlm.nih.gov/pubmed/35592538
http://dx.doi.org/10.2147/IJGM.S363425
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author Wu, Xiaoqiong
Li, Pu
Yimiti, Maimaitiaili
Ye, Zhiqiu
Fang, Xuqian
Chen, Peizhan
Gu, Zhidong
author_facet Wu, Xiaoqiong
Li, Pu
Yimiti, Maimaitiaili
Ye, Zhiqiu
Fang, Xuqian
Chen, Peizhan
Gu, Zhidong
author_sort Wu, Xiaoqiong
collection PubMed
description BACKGROUND: Chromosome is the basic framework for eukaryotic cells to store genetic information, but certain genes exist in circulation, such as extrachromosomal circular DNA (eccDNA). The unique genetic characteristics and structure of eccDNA provide a new vision on the early diagnosis of cancer; however, whether eccDNA contributes to the early diagnosis and progression of lung cancer remains unclear. METHODS: We performed next-generation sequencing (NGS) analysis of eccDNA from the plasma of 6 lung adenocarcinoma (LUAD) patients. The data of plasma eccDNA of healthy people were obtained from public available database. We compared size distribution, chromosome origin, formation and expression patterns of eccDNA between LUAD patients and those of 6 healthy people and 4 healthy gravidas. RESULTS: A total number of 716,059 eccDNA ranging from 22 bp to 3,297,519 bp were detected with an average size less than 800bp and distinctive bimodality in size around 191 bp and 320 bp. After comparison of eccDNA abundance in each sequencing sample, nine eccDNA were ranked on top with higher frequency in lung adenocarcinoma patients than healthy people. Among them, four eccDNA (DOCK1, PPIC, TBC1D16, and RP11-370A5.1) were uniquely expressed in lung adenocarcinoma patients, which may serve as potential biomarkers for early diagnosis LUAD. CONCLUSION: Cancer-specific eccDNA was presented in LUAD compared to normal people, which might serve as a promising biomarker in LUAD.
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spelling pubmed-91134592022-05-18 Identification and Characterization of Extrachromosomal Circular DNA in Plasma of Lung Adenocarcinoma Patients Wu, Xiaoqiong Li, Pu Yimiti, Maimaitiaili Ye, Zhiqiu Fang, Xuqian Chen, Peizhan Gu, Zhidong Int J Gen Med Original Research BACKGROUND: Chromosome is the basic framework for eukaryotic cells to store genetic information, but certain genes exist in circulation, such as extrachromosomal circular DNA (eccDNA). The unique genetic characteristics and structure of eccDNA provide a new vision on the early diagnosis of cancer; however, whether eccDNA contributes to the early diagnosis and progression of lung cancer remains unclear. METHODS: We performed next-generation sequencing (NGS) analysis of eccDNA from the plasma of 6 lung adenocarcinoma (LUAD) patients. The data of plasma eccDNA of healthy people were obtained from public available database. We compared size distribution, chromosome origin, formation and expression patterns of eccDNA between LUAD patients and those of 6 healthy people and 4 healthy gravidas. RESULTS: A total number of 716,059 eccDNA ranging from 22 bp to 3,297,519 bp were detected with an average size less than 800bp and distinctive bimodality in size around 191 bp and 320 bp. After comparison of eccDNA abundance in each sequencing sample, nine eccDNA were ranked on top with higher frequency in lung adenocarcinoma patients than healthy people. Among them, four eccDNA (DOCK1, PPIC, TBC1D16, and RP11-370A5.1) were uniquely expressed in lung adenocarcinoma patients, which may serve as potential biomarkers for early diagnosis LUAD. CONCLUSION: Cancer-specific eccDNA was presented in LUAD compared to normal people, which might serve as a promising biomarker in LUAD. Dove 2022-05-09 /pmc/articles/PMC9113459/ /pubmed/35592538 http://dx.doi.org/10.2147/IJGM.S363425 Text en © 2022 Wu et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Wu, Xiaoqiong
Li, Pu
Yimiti, Maimaitiaili
Ye, Zhiqiu
Fang, Xuqian
Chen, Peizhan
Gu, Zhidong
Identification and Characterization of Extrachromosomal Circular DNA in Plasma of Lung Adenocarcinoma Patients
title Identification and Characterization of Extrachromosomal Circular DNA in Plasma of Lung Adenocarcinoma Patients
title_full Identification and Characterization of Extrachromosomal Circular DNA in Plasma of Lung Adenocarcinoma Patients
title_fullStr Identification and Characterization of Extrachromosomal Circular DNA in Plasma of Lung Adenocarcinoma Patients
title_full_unstemmed Identification and Characterization of Extrachromosomal Circular DNA in Plasma of Lung Adenocarcinoma Patients
title_short Identification and Characterization of Extrachromosomal Circular DNA in Plasma of Lung Adenocarcinoma Patients
title_sort identification and characterization of extrachromosomal circular dna in plasma of lung adenocarcinoma patients
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9113459/
https://www.ncbi.nlm.nih.gov/pubmed/35592538
http://dx.doi.org/10.2147/IJGM.S363425
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