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Metagenomic Analysis of Serum Microbe-Derived Extracellular Vesicles and Diagnostic Models to Differentiate Ovarian Cancer and Benign Ovarian Tumor

We aimed to develop a diagnostic model identifying ovarian cancer (OC) from benign ovarian tumors using metagenomic data from serum microbe-derived extracellular vesicles (EVs). We obtained serum samples from 166 patients with pathologically confirmed OC and 76 patients with benign ovarian tumors. F...

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Autores principales: Kim, Se Ik, Kang, Nayeon, Leem, Sangseob, Yang, Jinho, Jo, HyunA, Lee, Maria, Kim, Hee Seung, Dhanasekaran, Danny N., Kim, Yoon-Keun, Park, Taesung, Song, Yong Sang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7281409/
https://www.ncbi.nlm.nih.gov/pubmed/32455705
http://dx.doi.org/10.3390/cancers12051309
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author Kim, Se Ik
Kang, Nayeon
Leem, Sangseob
Yang, Jinho
Jo, HyunA
Lee, Maria
Kim, Hee Seung
Dhanasekaran, Danny N.
Kim, Yoon-Keun
Park, Taesung
Song, Yong Sang
author_facet Kim, Se Ik
Kang, Nayeon
Leem, Sangseob
Yang, Jinho
Jo, HyunA
Lee, Maria
Kim, Hee Seung
Dhanasekaran, Danny N.
Kim, Yoon-Keun
Park, Taesung
Song, Yong Sang
author_sort Kim, Se Ik
collection PubMed
description We aimed to develop a diagnostic model identifying ovarian cancer (OC) from benign ovarian tumors using metagenomic data from serum microbe-derived extracellular vesicles (EVs). We obtained serum samples from 166 patients with pathologically confirmed OC and 76 patients with benign ovarian tumors. For model construction and validation, samples were randomly divided into training and test sets in the ratio 2:1. Isolation of microbial EVs from serum samples of the patients and 16S rDNA amplicon sequencing were carried out. Metagenomic and clinicopathologic data-based OC diagnostic models were constructed in the training set and then validated in the test set. There were significant differences in the metagenomic profiles between the OC and benign ovarian tumor groups; specifically, genus Acinetobacter was significantly more abundant in the OC group. More importantly, Acinetobacter was the only common genus identified by seven different statistical analysis methods. Among the various metagenomic and clinicopathologic data-based OC diagnostic models, the model consisting of age, serum CA-125 levels, and relative abundance of Acinetobacter showed the best diagnostic performance with the area under the receiver operating characteristic curve of 0.898 and 0.846 in the training and test sets, respectively. Thus, our findings establish a metagenomic analysis of serum microbe-derived EVs as a potential tool for the diagnosis of OC.
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spelling pubmed-72814092020-06-19 Metagenomic Analysis of Serum Microbe-Derived Extracellular Vesicles and Diagnostic Models to Differentiate Ovarian Cancer and Benign Ovarian Tumor Kim, Se Ik Kang, Nayeon Leem, Sangseob Yang, Jinho Jo, HyunA Lee, Maria Kim, Hee Seung Dhanasekaran, Danny N. Kim, Yoon-Keun Park, Taesung Song, Yong Sang Cancers (Basel) Article We aimed to develop a diagnostic model identifying ovarian cancer (OC) from benign ovarian tumors using metagenomic data from serum microbe-derived extracellular vesicles (EVs). We obtained serum samples from 166 patients with pathologically confirmed OC and 76 patients with benign ovarian tumors. For model construction and validation, samples were randomly divided into training and test sets in the ratio 2:1. Isolation of microbial EVs from serum samples of the patients and 16S rDNA amplicon sequencing were carried out. Metagenomic and clinicopathologic data-based OC diagnostic models were constructed in the training set and then validated in the test set. There were significant differences in the metagenomic profiles between the OC and benign ovarian tumor groups; specifically, genus Acinetobacter was significantly more abundant in the OC group. More importantly, Acinetobacter was the only common genus identified by seven different statistical analysis methods. Among the various metagenomic and clinicopathologic data-based OC diagnostic models, the model consisting of age, serum CA-125 levels, and relative abundance of Acinetobacter showed the best diagnostic performance with the area under the receiver operating characteristic curve of 0.898 and 0.846 in the training and test sets, respectively. Thus, our findings establish a metagenomic analysis of serum microbe-derived EVs as a potential tool for the diagnosis of OC. MDPI 2020-05-21 /pmc/articles/PMC7281409/ /pubmed/32455705 http://dx.doi.org/10.3390/cancers12051309 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kim, Se Ik
Kang, Nayeon
Leem, Sangseob
Yang, Jinho
Jo, HyunA
Lee, Maria
Kim, Hee Seung
Dhanasekaran, Danny N.
Kim, Yoon-Keun
Park, Taesung
Song, Yong Sang
Metagenomic Analysis of Serum Microbe-Derived Extracellular Vesicles and Diagnostic Models to Differentiate Ovarian Cancer and Benign Ovarian Tumor
title Metagenomic Analysis of Serum Microbe-Derived Extracellular Vesicles and Diagnostic Models to Differentiate Ovarian Cancer and Benign Ovarian Tumor
title_full Metagenomic Analysis of Serum Microbe-Derived Extracellular Vesicles and Diagnostic Models to Differentiate Ovarian Cancer and Benign Ovarian Tumor
title_fullStr Metagenomic Analysis of Serum Microbe-Derived Extracellular Vesicles and Diagnostic Models to Differentiate Ovarian Cancer and Benign Ovarian Tumor
title_full_unstemmed Metagenomic Analysis of Serum Microbe-Derived Extracellular Vesicles and Diagnostic Models to Differentiate Ovarian Cancer and Benign Ovarian Tumor
title_short Metagenomic Analysis of Serum Microbe-Derived Extracellular Vesicles and Diagnostic Models to Differentiate Ovarian Cancer and Benign Ovarian Tumor
title_sort metagenomic analysis of serum microbe-derived extracellular vesicles and diagnostic models to differentiate ovarian cancer and benign ovarian tumor
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7281409/
https://www.ncbi.nlm.nih.gov/pubmed/32455705
http://dx.doi.org/10.3390/cancers12051309
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